Donor Profile : Donor 50070

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Donor ID: 50070

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Meet The Donor

Donor 50070 loves money, but not in the way you might think. He wants to learn all he can about current markets and personal finance. On the flip side, he loves the outdoors just as much. In his spare time, you'll find him hiking, rock climbing, or even taking a leisurely walk. He's happy doing it all!

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Genetic Testing Performed: Please review the list of genetic tests performed before choosing a donor because donors have different levels of testing. Genetics is very complicated and testing can only reduce but not eliminate the risk of a donor being a carrier of a particular condition.


Any potential new health information will be indicated here. Please check periodically for medical updates. This profile is current as of:
May 20, 2025 10:20 AM EST


Document ID: 5C1D7D17E688B9CA1133B4AEBDDA7DEAC73EAED8CC1B8545386D9F5E1C383892

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Donor's "Name": Apollo

Year of Birth: 2002

Marital Status: Single

Number of Children: 0

Occupation:
(last reported)
Student

Education: Bachelor of Arts, Finance

Blood Type: A +

Nationality:
(self reported)
Maternal: Scottish
Paternal: Swiss

Race: White Or Caucasian

CMV Status: NEG
Learn More

Last Medical History Update: 03/17/2025

  • Reported Pregnancy/Birth
  • xyIdentity Disclosure
  • Available Inventory
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ADDITIONAL DONOR DETAILS

  • Height:
    5'9" (175.26 cm)
    Weight:
    163 lbs (74 kg)
    Eye Color:
    Brown
    Hair Color:
    Red, Dark
    Hair Texture:
    Thick
    Hair Loss:
    None
    Hair Type:
    Wavy
    Body Build:
    Medium
    Freckles:
    Few
    Skin Tone:
    Fair
  • ADVISORY

    This donor is a carrier of one or more genetic conditions.

    The list below includes the condition(s) that the donor carries. To view a complete list of the genes included in the donor's carrier testing click the relevant link below. To download the donor's test reports click the relevant link below. To purchase this donor's sperm, the intended parent/recipient must sign an acknowledgement form. For more information, please contact us.

    Over the years, Xytex has expanded genetic testing of donors as genetic knowledge and technology have advanced. As a result, not all donors have been tested for the same conditions or with the same methods. For more information about genetic testing view our Genetics FAQs.

    This donor has been evaluated for carrier status of the listed conditions. A negative result reduces, but does not eliminate, the likelihood of the donor being a carrier. If you are a known carrier of a genetic condition, please use the advanced search features to find donors who have tested negative for the condition(s) that you carry. Click the relevant link below to download the donor's test reports to share with your physician and/or genetic counselor.

    This donor's carrier testing included 301 genes.

    Biotinidase Deficiency (BTD)
    Carrier
    Hereditary Hemochromatosis Type 1 (HFE)
    Carrier
    21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
    No disease-causing variants detected
    3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (HMGCL)
    No disease-causing variants detected
    3-Methylcrotonyl-CoA Carboxylase Deficiency, MCCC1-Related (MCCC1)
    No disease-causing variants detected
    3-Methylcrotonyl-CoA Carboxylase Deficiency, MCCC2-Related (MCCC2)
    No disease-causing variants detected
    3-Methylglutaconic Aciduria Type III also known as Costeff Optic Atrophy (OPA3)
    No disease-causing variants detected
    3-Phosphoglycerate Dehydrogenase Deficiency, PHGDH-Related (PHGDH)
    No disease-causing variants detected
    6-Pyruvoyl-Tetrahydropterin Synthase Deficiency (PTS)
    No disease-causing variants detected
    Abetalipoproteinemia (MTTP)
    No disease-causing variants detected
    Achromatopsia (CNGB3)
    No disease-causing variants detected
    Acrodermatitis Enteropathica (SLC39A4)
    No disease-causing variants detected
    Acute Infantile Liver Failure (TRMU)
    No disease-causing variants detected
    Acyl-CoA Oxidase I Deficiency (ACOX1)
    No disease-causing variants detected
    Adenosine Deaminase Deficiency (ADA)
    No disease-causing variants detected
    Adrenoleukodystrophy, X-Linked (ABCD1)
    No disease-causing variants detected
    Aicardi-Goutieres Syndrome (SAMHD1)
    No disease-causing variants detected
    Aldosterone Synthase Deficiency also known as Corticosterone Methyloxidase Deficiency (CYP11B2)
    No disease-causing variants detected
    Alkaptonuria (HGD)
    No disease-causing variants detected
    Alpha-1 Antitrypsin Deficiency (SERPINA1)
    No disease-causing variants detected
    Alpha-Mannosidosis (MAN2B1)
    No disease-causing variants detected
    Alpha-Thalassemia (HBA1/HBA2)
    No disease-causing mutations detected; normal hemoglobin analysis
    Alpha-Thalassemia Intellectual Disability Syndrome, X-Linked (ATRX)
    No disease-causing variants detected
    Alport Syndrome, COL4A3-Related (COL4A3)
    No disease-causing variants detected
    Alport Syndrome, COL4A4-Related (COL4A4)
    No disease-causing variants detected
    Alport Syndrome, X-Linked (COL4A5)
    No disease-causing variants detected
    Alstrom Syndrome (ALMS1)
    No disease-causing variants detected
    Andermann Syndrome (SLC12A6)
    No disease-causing variants detected
    Arginase Deficiency also known as Argininemia (ARG1)
    No disease-causing variants detected
    Argininosuccinic Aciduria (ASL)
    No disease-causing variants detected
    Aromatase Deficiency (CYP19A1)
    No disease-causing variants detected
    Arthrogryposis, Mental Retardation, and Seizures (SLC35A3)
    No disease-causing variants detected
    Asparagine Synthetase Deficiency (ASNS)
    No disease-causing variants detected
    Aspartylglucosaminuria (AGA)
    No disease-causing variants detected
    Ataxia With Vitamin E Deficiency (TTPA)
    No disease-causing variants detected
    Ataxia-Telangiectasia (ATM)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS1-Related (BBS1)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS10-Related (BBS10)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS12-Related (BBS12)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS2-Related (BBS2)
    No disease-causing variants detected
    Bartter Syndrome, Type 4A (BSND)
    No disease-causing variants detected
    Bernard-Soulier Syndrome, Type A1 (GP1BA)
    No disease-causing variants detected
    Bernard-Soulier Syndrome, Type C (GP9)
    No disease-causing variants detected
    Beta-Ketothiolase Deficiency (ACAT1)
    No disease-causing variants detected
    Beta-Thalassemia, Sickle Cell Disease, and Beta-Globin Disorders (HBB)
    No disease-causing mutations detected; normal hemoglobin analysis
    Bloom Syndrome (BLM)
    No disease-causing variants detected
    Canavan Disease (ASPA)
    No disease-causing variants detected
    Carbamoylphosphate Synthetase I Deficiency (CPS1)
    No disease-causing variants detected
    Carnitine Palmitoyltransferase IA Deficiency (CPT1A)
    No disease-causing variants detected
    Carnitine Palmitoyltransferase II Deficiency (CPT2)
    No disease-causing variants detected
    Carpenter Syndrome (RAB23)
    No disease-causing variants detected
    Cartilage-Hair Hypoplasia (RMRP)
    No disease-causing variants detected
    Cerebral Creatine Deficiency Syndrome 1, X-Linked (SLC6A8)
    No disease-causing variants detected
    Cerebrotendinous Xanthomatosis (CYP27A1)
    No disease-causing variants detected
    Charcot-Marie-Tooth Disease, Type 4D (NDRG1)
    No disease-causing variants detected
    Charcot-Marie-Tooth Disease, Type 5 / Arts Syndrome, X-Linked (PRPS1)
    No disease-causing variants detected
    Charcot-Marie-Tooth Disease, X-Linked (GJB1)
    No disease-causing variants detected
    Choreoacanthocytosis (VPS13A)
    No disease-causing variants detected
    Choroidemia, X-Linked (CHM)
    No disease-causing variants detected
    Chromosome Analysis (Karyotype)
    Normal male karyotype
    Chronic Granulomatous Disease, CYBA-Related (CYBA)
    No disease-causing variants detected
    Chronic Granulomatous Disease, CYBB-Related, X-Linked (CYBB)
    No disease-causing variants detected
    Citrin Deficiency (SLC25A13)
    No disease-causing variants detected
    Citrullinemia Type 1 (ASS1)
    No disease-causing variants detected
    Cockayne Syndrome Type A (ERCC8)
    No disease-causing variants detected
    Cockayne Syndrome Type B (ERCC6)
    No disease-causing variants detected
    Cohen Syndrome (VPS13B)
    No disease-causing variants detected
    Combined Malonic and Methylmalonic Aciduria (ACSF3)
    No disease-causing variants detected
    Combined Oxidative Phosphorylation Deficiency 1 (GFM1)
    No disease-causing variants detected
    Combined Oxidative Phosphorylation Deficiency 3 (TSFM)
    No disease-causing variants detected
    Combined Pituitary Hormone Deficiency 2 (PROP1)
    No disease-causing variants detected
    Combined Pituitary Hormone Deficiency 3 (LHX3)
    No disease-causing variants detected
    Combined SAP Deficiency (PSAP)
    No disease-causing variants detected
    Congenital Adrenal Hyperplasia due to 11-Beta-Hydroxylase Deficiency (CYP11B1)
    No disease-causing variants detected
    Congenital Adrenal Hyperplasia due to 17-Alpha-Hydroxylase Deficiency (CYP17A1)
    No disease-causing variants detected
    Congenital Adrenal Hyperplasia due to 3-Beta-Hydroxysteroid Dehydrogenase Type II Deficiency (HSD3B2)
    No disease-causing variants detected
    Congenital Amegakaryocytic Thrombocytopenia (MPL)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation Type 1a, PMM2-Related (PMM2)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation Type 1b (MPI)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation, Type Ic (ALG6)
    No disease-causing variants detected
    Congenital Insensitivity to Pain with Anhidrosis (NTRK1)
    No disease-causing variants detected
    Congenital Myasthenic Syndrome (CHRNE)
    No disease-causing variants detected
    Congenital Myasthenic Syndrome (RAPSN)
    No disease-causing variants detected
    Congenital Neutropenia (HAX1)
    No disease-causing variants detected
    Congenital Neutropenia, VPS45-Related (VPS45)
    No disease-causing variants detected
    Corneal Dystrophy and Perceptive Deafness (SLC4A11)
    No disease-causing variants detected
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing variants detected
    Cystinosis (CTNS)
    No disease-causing variants detected
    D-Bifunctional Protein Deficiency (HSD17B4)
    No disease-causing variants detected
    Deafness, Autosomal Recessive 77 (LOXHD1)
    No disease-causing variants detected
    Dyskeratosis Congenita, RTEL1-Related (RTEL1)
    No disease-causing variants detected
    Dystrophic Epidermolysis Bullosa (COL7A1)
    No disease-causing variants detected
    Dystrophinopathies, DMD-Related, X-Linked (DMD)
    No disease-causing variants detected
    Ehlers-Danlos Syndrome, Type VIIC (ADAMTS2)
    No disease-causing variants detected
    Ellis-Van Creveld Syndrome, EVC-Related (EVC)
    No disease-causing variants detected
    Ellis-Van Creveld Syndrome, EVC2-Related (EVC2)
    No disease-causing variants detected
    Emery-Dreifuss Muscular Dystrophy, X-Linked (EMD)
    No disease-causing variants detected
    Enhanced S-Cone Syndrome (NR2E3)
    No disease-causing variants detected
    Ethylmalonic Encephalopathy (ETHE1)
    No disease-causing variants detected
    F5-Related Disorders (F5)
    No disease-causing variants detected
    Fabry Disease, X-Linked (GLA)
    No disease-causing variants detected
    Factor IX Deficiency, X-Linked (F9)
    No disease-causing variants detected
    Factor XI Deficiency (F11)
    No disease-causing variants detected
    Familial Dysautonomia (ELP1)
    No disease-causing variants detected
    Familial Hypercholesterolemia (LDLR)
    No disease-causing variants detected
    Familial Hypercholesterolemia (LDLRAP1)
    No disease-causing variants detected
    Familial Hyperinsulinism and Other ABCC8-Related Disorders (ABCC8)
    No disease-causing variants detected
    Familial Hyperinsulinism and Other KCNJ11-Related Disorders (KCNJ11)
    No disease-causing variants detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing variants detected
    Fanconi Anemia Type A (FANCA)
    No disease-causing variants detected
    Fanconi Anemia Type C (FANCC)
    No disease-causing variants detected
    Fanconi Anemia, Type G (FANCG)
    No disease-causing variants detected
    FKTN-Related Disorders including Walker-Warburg Syndrome (FKTN)
    No disease-causing variants detected
    Fragile X Syndrome, X-Linked (FMR1)
    No disease-causing mutations detected; CGG repeat number within normal range
    Fumarase Deficiency (FH)
    No disease-causing variants detected
    Galactokinase Deficiency (GALK1)
    No disease-causing variants detected
    Galactosemia, GALT-Related (GALT)
    No disease-causing variants detected
    Gaucher Disease (GBA)
    No disease-causing variants detected
    Gitelman Syndrome (SLC12A3)
    No disease-causing variants detected
    GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2)
    No disease-causing variants detected
    Glucose-6-Phosphate Dehydrogenase Deficiency, X-Linked (G6PD)
    No disease-causing variants detected
    Glutaric Acidemia Type 1 (GCDH)
    No disease-causing variants detected
    Glutaric Acidemia, Type IIa (ETFA)
    No disease-causing variants detected
    Glutaric Acidemia, Type IIc (ETFDH)
    No disease-causing variants detected
    Glycine Encephalopathy, AMT-Related (AMT)
    No disease-causing variants detected
    Glycine Encephalopathy, GLDC-Related (GLDC)
    No disease-causing variants detected
    Glycogen Storage Disease Type Ia (G6PC)
    No disease-causing variants detected
    Glycogen Storage Disease Type Ib (SLC37A4)
    No disease-causing variants detected
    Glycogen Storage Disease Type III (AGL)
    No disease-causing variants detected
    Glycogen Storage Disease Type V (PYGM)
    No disease-causing variants detected
    Glycogen Storage Disease, Type IV also known as Adult Polyglucosan Body Disease (GBE1)
    No disease-causing variants detected
    Glycogen Storage Disease, Type VII (PFKM)
    No disease-causing variants detected
    GRACILE Syndrome (BCS1L)
    No disease-causing variants detected
    Guanidinoacetate Methyltransferase Deficiency also known as Cerebral Creatine Deficiency Syndrome 2 (GAMT)
    No disease-causing variants detected
    Hemochromatosis, Type 3 (TFR2)
    No disease-causing variants detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing variants detected
    Hereditary Hemochromatosis (HJV)
    No disease-causing variants detected
    Hereditary Spastic Paraparesis 49 (TECPR2)
    No disease-causing variants detected
    Hermansky-Pudlak Syndrome, Type 1 (HPS1)
    No disease-causing variants detected
    Hermansky-Pudlak Syndrome, Type 3 (HPS3)
    No disease-causing variants detected
    Holocarboxylase Synthetase Deficiency (HLCS)
    No disease-causing variants detected
    Homocystinuria (CBS)
    No disease-causing variants detected
    Homocystinuria due to MTHFR Deficiency (MTHFR)
    No disease-causing variants detected
    Homocystinuria, Cobalamin E Type (MTRR)
    No disease-causing variants detected
    Hydrolethalus Syndrome (HYLS1)
    No disease-causing variants detected
    Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome (SLC25A15)
    No disease-causing variants detected
    Hypohidrotic Ectodermal Dysplasia, X-Linked (EDA)
    No disease-causing variants detected
    Hypophosphatasia, Autosomal Recessive (ALPL)
    No disease-causing variants detected
    Inclusion Body Myopathy 2 (GNE)
    No disease-causing variants detected
    Isovaleric Acidemia (IVD)
    No disease-causing variants detected
    Joubert Syndrome 2 (TMEM216)
    No disease-causing variants detected
    Joubert Syndrome 7 also known as Meckel Syndrome 5 (RPGRIP1L)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa (LAMA3)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa (LAMB3)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa (LAMC2)
    No disease-causing variants detected
    Juvenile Retinoschisis, X-Linked (RS1)
    No disease-causing variants detected
    Krabbe Disease (GALC)
    No disease-causing variants detected
    Leber Congenital Amaurosis 10 and Other CEP290-Related Ciliopathies (CEP290)
    No disease-causing variants detected
    Leber Congenital Amaurosis 13 (RDH12)
    No disease-causing variants detected
    Leber Congenital Amaurosis 2 also known as Retinitis Pigmentosa 20 (RPE65)
    No disease-causing variants detected
    Leber Congenital Amaurosis 5 (LCA5)
    No disease-causing variants detected
    Leber Congenital Amaurosis 8 also known as Retinitis Pigmentosa 12 (CRB1)
    No disease-causing variants detected
    Leigh Syndrome, French-Canadian Type (LRPPRC)
    No disease-causing variants detected
    Lethal Congenital Contracture Syndrome 1 (GLE1)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2A also known as Calpainopathy (CAPN3)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2B also known as Dysferlinopathy (DYSF)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2C also known as Gamma-Sarcoglycanopathy (SGCG)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2D also known as Alpha-Sarcoglycanopathy (SGCA)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2E also known as Beta-Sarcoglycanopathy (SGCB)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2I (FKRP)
    No disease-causing variants detected
    Lipoid Adrenal Hyperplasia (STAR)
    No disease-causing variants detected
    Lipoprotein Lipase Deficiency (LPL)
    No disease-causing variants detected
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    No disease-causing variants detected
    Lysinuric Protein Intolerance (SLC7A7)
    No disease-causing variants detected
    Lysosomal Acid Lipase Deficiency including Wolman Disease and Cholesteryl Ester Storage Disease (LIPA)
    No disease-causing variants detected
    Major Histocompatibility Complex Class II Deficiency also known as Bare Lymphocyte Syndrome Type II (CIITA)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 1A (BCKDHA)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 1B (BCKDHB)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 2 (DBT)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing variants detected
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing variants detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts Type 1 (MLC1)
    No disease-causing variants detected
    Menkes Disease and Other ATP7A-Related Disorders, X-Linked (ATP7A)
    No disease-causing variants detected
    Merosin-Deficient Muscular Dystrophy (LAMA2)
    No disease-causing variants detected
    Metachromatic Leukodystrophy (ARSA)
    No disease-causing variants detected
    Methylmalonic Acidemia (MMAA)
    No disease-causing variants detected
    Methylmalonic Acidemia (MMAB)
    No disease-causing variants detected
    Methylmalonic Acidemia (MUT)
    No disease-causing variants detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin C Type (MMACHC)
    No disease-causing variants detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin D Type (MMADHC)
    No disease-causing variants detected
    Microphthalmia and Anophthalmia (VSX2)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency (ACAD9)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency 16 (NDUFAF5)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency, NDUFS6-Related (NDUFS6)
    No disease-causing variants detected
    Mitochondrial DNA Depletion Syndrome 6 also known as Navajo Neurohepatopathy (MPV17)
    No disease-causing variants detected
    Mitochondrial Myopathy and Sideroblastic Anemia 1 (PUS1)
    No disease-causing variants detected
    Mitochondrial Neurogastrointestinal Encephalopathy Disease (TYMP)
    No disease-causing variants detected
    MKS1-Related Disorders, including Bardet-Biedl Syndrome 13, Joubert Syndrome 28, and Meckel Syndrome 1 (MKS1)
    No disease-causing variants detected
    Mucolipidosis II and IIIA (GNPTAB)
    No disease-causing variants detected
    Mucolipidosis III Gamma (GNPTG)
    No disease-causing variants detected
    Mucolipidosis Type IV (MCOLN1)
    No disease-causing variants detected
    Mucopolysaccharidosis Type I also known as Hurler Syndrome (IDUA)
    No disease-causing variants detected
    Mucopolysaccharidosis Type II also known as Hunter Syndrome, X-Linked (IDS)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IIIA also known as Sanfilippo A Syndrome (SGSH)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IIIB also known as Sanfilippo B Syndrome (NAGLU)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IIIC also known as Sanfilippo C Syndrome (HGSNAT)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IIID (GNS)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IVb also known as GM1 Gangliosidosis (GLB1)
    No disease-causing variants detected
    Mucopolysaccharidosis Type VI (ARSB)
    No disease-causing variants detected
    Mucopolysaccharidosistype IX (HYAL1)
    No disease-causing variants detected
    Multiple Sulphatase Deficiency (SUMF1)
    No disease-causing variants detected
    Muscle-Eye-Brain Disease (POMGNT1)
    No disease-causing variants detected
    Myotubular Myopathy, X-Linked (MTM1)
    No disease-causing variants detected
    N-Acetylglutamate Synthase Deficiency (NAGS)
    No disease-causing variants detected
    Nemaline Myopathy 2 (NEB)
    No disease-causing variants detected
    Nephrogenic Diabetes Insipidus, Type II (AQP2)
    No disease-causing variants detected
    Nephrotic Syndrome, NPHS1-Related also known as Congenital Finnish Nephrosis (NPHS1)
    No disease-causing variants detected
    Nephrotic Syndrome, NPHS2-Related also known as Steroid-Resistant Nephrotic Syndrome (NPHS2)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN3-Related (CLN3)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN5-Related (CLN5)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN6-Related (CLN6)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN8-Related also known as Northern Epilepsy (CLN8)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, MFSD8-Related (MFSD8)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, PPT1-Related (PPT1)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, TPP1-Related (TPP1)
    No disease-causing variants detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing variants detected
    Niemann-Pick Disease Type C, NPC1-Related (NPC1)
    No disease-causing variants detected
    Niemann-Pick Disease Type C, NPC2-Related (NPC2)
    No disease-causing variants detected
    Nijmegen Breakage Syndrome (NBN)
    No disease-causing variants detected
    Odonto-Onycho-Dermal Dysplasia also known as Schopf-Schulz-Passarge Syndrome (WNT10A)
    No disease-causing variants detected
    Omenn Syndrome and Severe Combined Immunodeficiency, Athabaskan-Type (DCLRE1C)
    No disease-causing variants detected
    Omenn Syndrome, RAG2-Related (RAG2)
    No disease-causing variants detected
    Ornithine Aminotransferase Deficiency (OAT)
    No disease-causing variants detected
    Ornithine Transcarbamylase Deficiency, X-Linked (OTC)
    No disease-causing variants detected
    Osteochondrodysplasias, Sulfate Transporter-Related (SLC26A2)
    No disease-causing variants detected
    Osteopetrosis Type 1 (TCIRG1)
    No disease-causing variants detected
    Pendred Syndrome (SLC26A4)
    No disease-causing variants detected
    Peroxisome Biogenesis Disorder, Type 3 (PEX12)
    No disease-causing variants detected
    Phenylalanine Hydroxylase Deficiency also known as Phenylketonuria (PAH)
    No disease-causing variants detected
    Polycystic Kidney Disease, Autosomal Recessive (PKHD1)
    No disease-causing variants detected
    Polyglandular Autoimmune Syndrome Type 1 (AIRE)
    No disease-causing variants detected
    Polymicrogyria (ADGRG1)
    No disease-causing variants detected
    Pompe Disease also known as Glycogen Storage Disease Type II (GAA)
    No disease-causing variants detected
    Pontocerebellar Hypoplasia Type 1A (VRK1)
    No disease-causing variants detected
    Pontocerebellar Hypoplasia Type 6 (RARS2)
    No disease-causing variants detected
    Postnatal Progressive Microcephaly also known as Infantile Cerebral and Cerebellar Atrophy (MED17)
    No disease-causing variants detected
    Primary Carnitine Deficiency (SLC22A5)
    No disease-causing variants detected
    Primary Ciliary Dyskinesia, DNAH5-Related (DNAH5)
    No disease-causing variants detected
    Primary Ciliary Dyskinesia, DNAI1-Related (DNAI1)
    No disease-causing variants detected
    Primary Ciliary Dyskinesia, DNAI2-Related (DNAI2)
    No disease-causing variants detected
    Primary Hyperoxaluria Type 1 (AGXT)
    No disease-causing variants detected
    Primary Hyperoxaluria Type 2 (GRHPR)
    No disease-causing variants detected
    Primary Hyperoxaluria, Type 3 (HOGA1)
    No disease-causing variants detected
    Progressive Cerebello-Cerebral Atrophy (SEPSECS)
    No disease-causing variants detected
    Progressive Familial Intrahepatic Cholestasis Type 2 (ABCB11)
    No disease-causing variants detected
    Propionic Acidemia, PCCA-Related (PCCA)
    No disease-causing variants detected
    Propionic Acidemia, PCCB-Related (PCCB)
    No disease-causing variants detected
    Prothrombin-Related Thrombophilia (F2)
    No disease-causing variants detected
    Pycnodysostosis (CTSK)
    No disease-causing variants detected
    Pyruvate Carboxylase Deficiency (PC)
    No disease-causing variants detected
    Pyruvate Dehydrogenase E1-Alpha Deficiency, X-Linked (PDHA1)
    No disease-causing variants detected
    Pyruvate Dehydrogenase E1-Beta Deficiency (PDHB)
    No disease-causing variants detected
    Renal Tubular Acidosis and Deafness (ATP6V1B1)
    No disease-causing variants detected
    Retinitis Pigmentosa 25 (EYS)
    No disease-causing variants detected
    Retinitis Pigmentosa 26 (CERKL)
    No disease-causing variants detected
    Retinitis Pigmentosa 28 (FAM161A)
    No disease-causing variants detected
    Retinitis Pigmentosa 59 (DHDDS)
    No disease-causing variants detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing variants detected
    Rhizomelic Chondrodysplasia Punctata Type 3 (AGPS)
    No disease-causing variants detected
    Roberts Syndrome (ESCO2)
    No disease-causing variants detected
    Salla Disease (SLC17A5)
    No disease-causing variants detected
    Sandhoff Disease (HEXB)
    No disease-causing variants detected
    Schimke Immunoosseous Dysplasia (SMARCAL1)
    No disease-causing variants detected
    Severe Combined Immunodeficiency, X-Linked (IL2RG)
    No disease-causing variants detected
    Sjogren-Larsson Syndrome (ALDH3A2)
    No disease-causing variants detected
    Smith-Lemli-Opitz Syndrome (DHCR7)
    No disease-causing variants detected
    Spastic Ataxia of Charlevoix-Saguenay, Autosomal Recessive (SACS)
    No disease-causing variants detected
    Spastic Paraplegia, Type 15 (ZFYVE26)
    No disease-causing variants detected
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Spondylothoracic Dysostosis (MESP2)
    No disease-causing variants detected
    Steel Syndrome (COL27A1)
    No disease-causing variants detected
    Stuve-Wiedemann Syndrome (LIFR)
    No disease-causing variants detected
    Tay-Sachs Disease also known as Hexosaminidase A Deficiency (HEXA)
    No disease-causing variants detected
    TGM1-Related Autosomal Recessive Congenital Ichthyosis (TGM1)
    No disease-causing variants detected
    Tyrosine Hydroxylase Deficiency (TH)
    No disease-causing variants detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing variants detected
    Tyrosinemia, Type II (TAT)
    No disease-causing variants detected
    Usher Syndrome Type IB (MYO7A)
    No disease-causing variants detected
    Usher Syndrome Type IC (USH1C)
    No disease-causing variants detected
    Usher Syndrome Type ID (CDH23)
    No disease-causing variants detected
    Usher Syndrome Type IF (PCDH15)
    No disease-causing variants detected
    Usher Syndrome Type IIA (USH2A)
    No disease-causing variants detected
    Usher Syndrome Type IIIA (CLRN1)
    No disease-causing variants detected
    Vanishing White Matter Disease (EIF2B5)
    No disease-causing variants detected
    Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
    No disease-causing variants detected
    Wilson Disease (ATP7B)
    No disease-causing variants detected
    Xeroderma Pigmentosum, Group A (XPA)
    No disease-causing variants detected
    Xeroderma Pigmentosum, Group C (XPC)
    No disease-causing variants detected
    Zellweger Spectrum Disorder, PEX2-Related (PEX2)
    No disease-causing variants detected
    Zellweger Spectrum Disorder, PEX6-Related (PEX6)
    No disease-causing variants detected
    Zellweger Syndrome Spectrum (PEX1)
    No disease-causing variants detected
    Zellweger Syndrome Spectrum, PEX10- Related (PEX10)
    No disease-causing variants detected
  • Medication Allergy:
    No
    Food Allergy:
    No
    Pet Allergy:
    No
    Hay Fever Allergy:
    No
    Insect Allergy:
    No
    Vaccine Allergy:
    No
    Healthy Teeth:
    Yes
    Braces:
    Yes
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    Yes
    Chicken Pox Age:
    8
    Vertigo:
    No
    Eyesight Correction:
    No
    Near or Far Sighted:
    Skin Infection:
    No
    Gallstones:
    No
    Removed Gall Bladder:
    No
    Hernia:
    No
    Mumps:
    No
    Measles:
    No
    Measles Age:
    German Measles:
    No
    German Measles Age:
    Sinus Infection:
    No
    Stomach Ulcers:
    No
  • Skills, Hobbies and Interests:

  • In School:
    Yes
    Is the donor currently enrolled in or does the donor hold an undergraduate degree?
    Yes
    Degree Earned/Working towards:
    Bachelor of Arts
    Degree Status:
    Currently enrolled
    Major:
    Finance
    Minor:
    N/A
    Is the donor currently enrolled in or does the donor hold a graduate degree?
    No
    Is the donor currently enrolled in or does the donor hold a post graduate degree?
    No
    Is the donor currently enrolled in or does the donor have any specialized training (Including Military, Police, Firefighter, EMS, Real Estate, etc.)?
    No
  • The following medical conditions apply to the donor and his BLOOD RELATIVES ONLY (grandparents, parents, aunts, uncles, cousins, brothers, sisters, nieces, nephews and children of the donor).

    If a donor answers "yes" to any high-risk question on his Medical History Questionnaire, the donor is ineligible.

    Autoimmune Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    CREST Syndrome X
    Lupus X
    Scleroderma X
    Sjogren's Syndrome X
    Blood Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Anemia X
    Fanconi Anemia X
    Hemophilia X
    Immunodeficiency X
    Leukemia X
    Sickle Cell X
    Thalassemia X
    Von Willebrand's disease X
    Cancer Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Cancer (Breast) X
    Cancer (Colon) X
    Cancer (Leukemia) X
    Cancer (Lung) X
    Cancer (Other) X
    Cancer (Skin) X
    Lymphoma X
    Melanoma X
    Prostate X
    Tumor X
    Cardio Vascular Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Congenital Heart Disease X
    Heart Attack X Grandfather X 80
    Heart Disease X
    High Blood Pressure X
    High Cholesterol/Triglycerides X
    Stroke X Grandfather X 75
    Cardio Vascular (Other) X
    Congenital Malformations Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Deviated Septum X
    Malformations (Cleft Lip) X
    Malformations (Cleft Palate) X
    Malformations (Club Foot) X
    Malformations (Hypospadias) X
    Malformations (Other) X
    Malformations (Polydactyly) X
    Malformations (Syndactyly) X
    Undescended Testicles X
    Gastro-Intestinal Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Gallstones X
    GI (Crohn's) X
    GI (Diverticulitis) X
    GI (Other) X
    GI (Pyloric Stenosis) X
    GI (Ulcerative Colitis) X
    GI (Ulcers) X
    Hemochromatosis X
    Hepatitis X
    Kidney Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Adrenal Hyperplasia X
    Born with 1 kidney X
    Kidney (Other) X
    Kidney disease or urinary tract disorder X
    Kidney Disorder X
    Polycystic Kidney Disease X
    Progressive Kidney Disease X
    Mental Health Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Anxiety disorder X
    Mental (Depression) X Father 51
    Mental (Manic Depressive) X
    Mental (Schizophrenia) X
    Mental Retardation X
    Obsessive-compulsive disorder X
    Metabolic/Endrocrine Dis. Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Diabetes (Insulin Dependent) X
    Diabetes (Non-Insulin Dependent) X
    Galactosemia X
    Gaucher's disease X
    Goiter X
    Hypoglycemia X
    Maple Syrup disease X
    PKU or Inherited Metabolic Disorder X
    Tay Sachs X
    Thyroid Disorder X
    Muscular/Bones/Joint Disease Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Achondroplasia (Dwarfism) X
    Arthritis (Other) X
    Congenital Hip Disease X
    Gout X
    Loss of Muscle Coordination X
    Marfan's Disease X
    Muscular Dystrophy X
    Osteoarthritis X
    Osteoporosis X
    Rheumatoid Arthritis X
    Scoliosis X
    Spinal Muscular Atrophy X
    Neurological Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Learning Disorder: ADD, ADHD, Dyslexia X Me 20
    Autism/ Asperger X
    Canavan's disease X
    Cerebral Palsy X
    Dementia X
    Disorders of the spinal cord X
    Dyslexia X
    Familial dysautonomia X
    Lesch-Nyhan Syndrome X
    Migraines X
    Mucolipidosis type IV X
    Neurologic (Alzheimer) X
    Neurologic (Creutzfeldt-Jakob Disease) X
    Neurologic (Epilepsy) X
    Neurologic (Guillain Barre) X
    Neurologic (Huntington's) X
    Neurologic (JC Virus) X
    Neurologic (Lou Gehrig's Disease) X
    Neurologic (Multiple Sclerosis) X
    Neurologic (Neural Tube Defect) X
    Neurologic (Neurofibromatosis) X
    Neurologic (Parkinson's Disease) X
    Neurologic (Subacute Sclerosing Panencephalitis) X
    Nieman-Pick X
    Spongiform encephalopathy/prion disease X
    Tourette Syndrome X
    Other Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Alcoholism X
    Bloom syndrome X
    Cystic Fibrosis X
    Down Syndrome X
    Drug Abuse X
    Encephalitis: viral or of unknown origin X
    Fragile X X
    Klinefelter X
    Meningitis X
    Noonan or Turner Syndrome X
    Early Death - Suicide X Father 51
    Other - Inherited Genetic Condition X
    Other Disease/Condition X
    Premature Organ Degeneration X
    Radiation Exposure X
    SIDS X
    Toxic Chemical Exposure X
    Turner's Syndrome X
    West Nile (suspected or confirmed by lab testing) X
    Respiratory Disease Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Allergies (Drug) X
    Allergies (Food) X
    Allergies (Hay Fever) X
    Allergies (Insect) X
    Allergies (Other) X
    Allergies (Pet) X
    Asthma X
    Emphysema X
    SARS X
    Tuberculosis X
    Sight/Sound/Smell Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Cataracts X
    Deafness X
    Deafness (before age 50) X
    Ear deformity X
    Eyesight (Blindness) X
    Eyesight (Red-Green Color Blindness) X
    Eyesight (Glaucoma) X
    Eyesight (Other) X
    Eyesight (Retinoblastoma) X
    Macular degeneration X
    Skin Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Albinism X
    Eczema X
    Pigmentation disorders (including Vitiligo) X
    Psoriasis X
    Skin Disease X
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Father
    Hair Color: Blonde, Medium Eyesight:
    Freckles: None Hair Texture:
    Health Status: Skin Tone: Medium Dominant Hand:
    Year of Birth: 1971 Cause of Death: Suicide Hair Loss: Receding
    Height: 6'" (182.88 cm) Age at Death: 51 Body Hair: Curly
    Weight: 250 lbs. (113 kg) Occupation: Sales Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision. Enjoyed fishing and hunting.
    FAMILY MEMBER: Mother
    Hair Color: Red, Light Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1975 Cause of Death: Hair Loss: Thinning
    Height: 5'05" (165.1 cm) Age at Death: Body Hair: Wavy
    Weight: 175 lbs. (79 kg) Occupation: Information Technology Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Pescatarian. Enjoys horseback riding.
    FAMILY MEMBER: Brother
    Hair Color: Red, Dark Eyesight:
    Freckles: Numerous Hair Texture: Thin
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 2006 Cause of Death: Hair Loss:
    Height: 6'" (182.88 cm) Age at Death: Body Hair: Wavy
    Weight: 160 lbs. (72 kg) Occupation: Student Eye Color: Brown, Dark
    Half Siblings: No Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Tech savvy. Enjoys video games.
    FAMILY MEMBER: Brother
    Hair Color: Black Eyesight:
    Freckles: Few Hair Texture: Fine
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 2000 Cause of Death: Hair Loss:
    Height: 6'" (182.88 cm) Age at Death: Body Hair:
    Weight: 215 lbs. (97 kg) Occupation: Welder Eye Color: Brown, Dark
    Half Siblings: No Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Avid reader. His interest is in philosophy.
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Brown, Medium Eyesight:
    Freckles: None Hair Texture:
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1939 Cause of Death: Heart Attack Hair Loss: Receding
    Height: 6'" (182.88 cm) Age at Death: 80 Body Hair: Straight
    Weight: 190 lbs. (86 kg) Occupation: Navy Captain Eye Color: Brown, Dark
    Half Siblings: Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision. Weapon specialist.
    FAMILY MEMBER: Grandmother
    Hair Color: Blonde, Light Eyesight:
    Freckles: None Hair Texture:
    Health Status: Fair Skin Tone: Fair Dominant Hand:
    Year of Birth: 1943 Cause of Death: Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: Body Hair: Curly
    Weight: 150 lbs. (68 kg) Occupation: Homemaker Eye Color: Brown, Dark
    Half Siblings: Education: College (Some) Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Enjoys cooking.
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1968 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Brown, Medium Eyesight:
    Freckles: None Hair Texture:
    Health Status: Skin Tone: Medium Dominant Hand:
    Year of Birth: 1945 Cause of Death: Stroke Hair Loss: Receding
    Height: 5'11" (180.34 cm) Age at Death: 75 Body Hair: Straight
    Weight: 180 lbs. (81 kg) Occupation: Former Air Force Pilot, Statistician Eye Color: Brown, Dark
    Half Siblings: Education: Masters Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision.
    FAMILY MEMBER: Grandmother
    Hair Color: Blonde, Dark Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1949 Cause of Death: Hair Loss: Thinning
    Height: 5'03" (160.02 cm) Age at Death: Body Hair: Straight
    Weight: 130 lbs. (59 kg) Occupation: Retired, Homemaker Eye Color: Brown, Dark
    Half Siblings: Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Enjoys art, painting, and sculpting.
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1965 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:

Purchase Bundle Options

Purchase Bundle Options

Vial Types Available for Donor #50070

All prices shown are in USD.

$1625 per vial Identity Disclosure xyGene Washed

$1625 per vial Identity Disclosure xyGene Unwashed

$1380 per vial Identity Disclosure xyGene ART

Due to inventory, above prices do not guarantee that listed vial types are currently available. Please contact our team to check availability.

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Purchasing vials from Xytex requires agreeing to and digitally signing the Xytex Services and Shipping Agreement and the ID Disclosure Agreement. At the time of checkout, you'll be prompted to digitally sign these documents. In addition, your order must be shipped to your healthcare facility's address. If you require your order to be shipped to a personal address, an additional agreement must be signed by your healthcare facility before your order can be shipped and your order may be delayed.