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Donor Profile : Donor 5607

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Donor ID: 5607

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Meet The Donor

Donor 5607's perfect day would be spent walking in Paris with his son, eating good food and taking in the sights. He's kind and funny, and classical music calms him when life gets hectic. He loves teaching more than just about anything, but he is also drawn to learning. He's currently pursuing his PhD!

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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:
June 3, 2023 7:58 PM EST


Document ID: C976977F185AAF13D4ADB6A046FB3CD2BC0804B3CC5DBADC0A6D2E15DF74EBD4

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Donor's "Name": Roger

Year of Birth: 1990

Marital Status: Married

Number of Children: 1

Occupation:
(last reported) RESEARCH ASSISTANT

Education: BACHELOR OF SCIENCE, ECONOMICS, MASTER OF SCIENCE, FINANCE, PHD, ECONOMICS

Blood Type: O +

Nationality:
(self reported) Maternal: Kazakh
Paternal: Russian

Race: White Or Caucasian

CMV Status: NEG
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Last Medical History Update: 05/11/2023

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

  • Height:
    5'7" (170.18 cm)
    Weight:
    154 lbs (69 kg)
    Eye Color:
    Green/Grey
    Hair Color:
    Brown
    Hair Texture:
    Fine
    Hair Loss:
    None
    Hair Type:
    Wavy
    Body Build:
    Medium
    Freckles:
    None
    Skin Tone:
    Fair

  • ADVISORY

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

    Below is a list of all conditions for which donor 5607 was tested, including the condition(s) of which he is a carrier. To purchase vials from this donor, the intended parent must sign an acknowledgment 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 contact us, and we will provide a copy of the donor's test reports to your physician and/or genetic counselor.

    This donor was tested for 284 conditions.

    Limb-Girdle Muscular Dystrophy Type 2A also known as Calpainopathy (CAPN3)
    Carrier
    21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
    No disease-causing mutations detected
    3-Hydroxy-3-Methylglutaryl-CoA (HMG-CoA) Lyase Deficiency (HMGCL)
    No disease-causing mutations detected
    3-Methylcrotonyl-CoA Carboxylase Deficiency, MCCC1-Related (MCCC1)
    No disease-causing mutations detected
    3-Methylcrotonyl-CoA Carboxylase Deficiency, MCCC2-Related (MCCC2)
    No disease-causing mutations detected
    3-Methylglutaconic Aciduria Type III also known as Costeff Optic Atrophy (OPA3)
    No disease-causing mutations detected
    3-Phosphoglycerate Dehydrogenase Deficiency, PHGDH-Related (PHGDH)
    No disease-causing mutations detected
    6-Pyruvoyl-Tetrahydropterin Synthase Deficiency (PTS)
    No disease-causing mutations detected
    Abetalipoproteinemia (MTTP)
    No disease-causing mutations detected
    Achromatopsia (CNGB3)
    No disease-causing mutations detected
    Acrodermatitis Enteropathica (SLC39A4)
    No disease-causing mutations detected
    Acute Infantile Liver Failure (TRMU)
    No disease-causing mutations detected
    Acyl-CoA Oxidase I Deficiency (ACOX1)
    No disease-causing mutations detected
    Adenosine Deaminase Deficiency (ADA)
    No disease-causing mutations detected
    Adrenoleukodystrophy, X-Linked (ABCD1)
    No disease-causing mutations detected
    Aicardi-Goutieres Syndrome (SAMHD1)
    No disease-causing mutations detected
    Aldosterone Synthase Deficiency also known as Corticosterone Methyloxidase Deficiency (CYP11B2)
    No disease-causing mutations detected
    Alpha-Mannosidosis (MAN2B1)
    No disease-causing mutations detected
    Alpha-Thalassemia (HBA1/HBA2)
    No disease-causing mutations detected; normal red blood cell indices and hemoglobin analysis
    Alpha-Thalassemia Intellectual Disability Syndrome, X-Linked (ATRX)
    No disease-causing mutations detected
    Alport Syndrome, COL4A3-Related (COL4A3)
    No disease-causing mutations detected
    Alport Syndrome, COL4A4-Related (COL4A4)
    No disease-causing mutations detected
    Alport Syndrome, X-Linked (COL4A5)
    No disease-causing mutations detected
    Alstrom Syndrome (ALMS1)
    No disease-causing mutations detected
    Andermann Syndrome (SLC12A6)
    No disease-causing mutations detected
    Argininosuccinic Aciduria (ASL)
    No disease-causing mutations detected
    Aromatase Deficiency (CYP19A1)
    No disease-causing mutations detected
    Arthrogryposis, Mental Retardation, and Seizures (SLC35A3)
    No disease-causing mutations detected
    Asparagine Synthetase Deficiency (ASNS)
    No disease-causing mutations detected
    Aspartylglucosaminuria (AGA)
    No disease-causing mutations detected
    Ataxia With Vitamin E Deficiency (TTPA)
    No disease-causing mutations detected
    Ataxia-Telangiectasia (ATM)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome 13 also known as Meckel Syndrome 1 (MKS1)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS1-Related (BBS1)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS10-Related (BBS10)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS12-Related (BBS12)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS2-Related (BBS2)
    No disease-causing mutations detected
    Bartter Syndrome, Type 4A (BSND)
    No disease-causing mutations detected
    Bernard-Soulier Syndrome, Type A1 (GP1BA)
    No disease-causing mutations detected
    Bernard-Soulier Syndrome, Type C (GP9)
    No disease-causing mutations detected
    Beta-Ketothiolase Deficiency (ACAT1)
    No disease-causing mutations detected
    Beta-Thalassemia, Sickle Cell Disease, and Beta-Globin Disorders (HBB)
    No disease-causing mutations detected; normal red blood cell indices and hemoglobin analysis
    Bilateral Frontoparietal Polymicrogyria (GPR56)
    No disease-causing mutations detected
    Biotinidase Deficiency (BTD)
    No disease-causing mutations detected
    Bloom Syndrome (BLM)
    No disease-causing mutations detected
    Canavan Disease (ASPA)
    No disease-causing mutations detected
    Carbamoylphosphate Synthetase I Deficiency (CPS1)
    No disease-causing mutations detected
    Carnitine Palmitoyltransferase IA Deficiency (CPT1A)
    No disease-causing mutations detected
    Carnitine Palmitoyltransferase II Deficiency (CPT2)
    No disease-causing mutations detected
    Carpenter Syndrome (RAB23)
    No disease-causing mutations detected
    Cartilage-Hair Hypoplasia (RMRP)
    No disease-causing mutations detected
    Cerebral Creatine Deficiency Syndrome 1 (SLC6A8)
    No disease-causing mutations detected
    Cerebrotendinous Xanthomatosis (CYP27A1)
    No disease-causing mutations detected
    Charcot-Marie-Tooth Disease, Type 4D (NDRG1)
    No disease-causing mutations detected
    Charcot-Marie-Tooth Disease, Type 5 / Arts Syndrome (PRPS1)
    No disease-causing mutations detected
    Charcot-Marie-Tooth Disease, X-Linked (GJB1)
    No disease-causing mutations detected
    Choreoacanthocytosis (VPS13A)
    No disease-causing mutations detected
    Choroidemia, X-Linked (CHM)
    No disease-causing mutations detected
    Chromosome Analysis (Karyotype)
    Normal male karyotype
    Chronic Granulomatous Disease, CYBA-Related (CYBA)
    No disease-causing mutations detected
    Chronic Granulomatous Disease, CYBB-Related (CYBB)
    No disease-causing mutations detected
    Citrin Deficiency (SLC25A13)
    No disease-causing mutations detected
    Citrullinemia Type 1 (ASS1)
    No disease-causing mutations detected
    Cohen Syndrome (VPS13B)
    No disease-causing mutations detected
    Combined Malonic and Methylmalonic Aciduria (ACSF3)
    No disease-causing mutations detected
    Combined Oxidative Phosphorylation Deficiency 1 (GFM1)
    No disease-causing mutations detected
    Combined Oxidative Phosphorylation Deficiency 3 (TSFM)
    No disease-causing mutations detected
    Combined Pituitary Hormone Deficiency 2 (PROP1)
    No disease-causing mutations detected
    Combined Pituitary Hormone Deficiency 3 (LHX3)
    No disease-causing mutations detected
    Combined SAP Deficiency (PSAP)
    No disease-causing mutations detected
    Congenital Adrenal Hyperplasia due to 17-Alpha-Hydroxylase Deficiency (CYP17A1)
    No disease-causing mutations detected
    Congenital Adrenal Hyperplasia due to 3-Beta-Hydroxysteroid Dehydrogenase Type II Deficiency (HSD3B2)
    No disease-causing mutations detected
    Congenital Amegakaryocytic Thrombocytopenia (MPL)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1a, PMM2-Related (PMM2)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1b (MPI)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation, Type Ic (ALG6)
    No disease-causing mutations detected
    Congenital Insensitivity to Pain with Anhidrosis (NTRK1)
    No disease-causing mutations detected
    Congenital Myasthenic Syndrome (CHRNE)
    No disease-causing mutations detected
    Congenital Myasthenic Syndrome (RAPSN)
    No disease-causing mutations detected
    Congenital Neutropenia (HAX1)
    No disease-causing mutations detected
    Congenital Neutropenia, VPS45-Related (VPS45)
    No disease-causing mutations detected
    Corneal Dystrophy and Perceptive Deafness (SLC4A11)
    No disease-causing mutations detected
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing mutations detected
    Cystinosis (CTNS)
    No disease-causing mutations detected
    D-Bifunctional Protein Deficiency (HSD17B4)
    No disease-causing mutations detected
    Deafness, Autosomal Recessive 77 (LOXHD1)
    No disease-causing mutations detected
    Dyskeratosis Congenita, RTEL1-Related (RTEL1)
    No disease-causing mutations detected
    Dystrophic Epidermolysis Bullosa (COL7A1)
    No disease-causing mutations detected
    Dystrophinopathies, DMD-Related, X-Linked (DMD)
    No disease-causing mutations detected
    Ehlers-Danlos Syndrome, Type VIIC (ADAMTS2)
    No disease-causing mutations detected
    Ellis-Van Creveld Syndrome, EVC-Related (EVC)
    No disease-causing mutations detected
    Emery-Dreifuss Muscular Dystrophy, X-Linked (EMD)
    No disease-causing mutations detected
    Enhanced S-Cone Syndrome (NR2E3)
    No disease-causing mutations detected
    Ethylmalonic Encephalopathy (ETHE1)
    No disease-causing mutations detected
    Fabry Disease, X-Linked (GLA)
    No disease-causing mutations detected
    Factor IX Deficiency, X-Linked (F9)
    No disease-causing mutations detected
    Factor XI Deficiency (F11)
    No disease-causing mutations detected
    Familial Dysautonomia (IKBKAP)
    No disease-causing mutations detected
    Familial Hypercholesterolemia (LDLR)
    No disease-causing mutations detected
    Familial Hypercholesterolemia (LDLRAP1)
    No disease-causing mutations detected
    Familial Hyperinsulinism and Other ABCC8-Related Disorders (ABCC8)
    No disease-causing mutations detected
    Familial Hyperinsulinism and Other KCNJ11-Related Disorders (KCNJ11)
    No disease-causing mutations detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing mutations detected
    Fanconi Anemia Type A (FANCA)
    No disease-causing mutations detected
    Fanconi Anemia Type C (FANCC)
    No disease-causing mutations detected
    Fanconi Anemia, Type G (FANCG)
    No disease-causing mutations detected
    FKTN-Related Disorders including Walker-Warburg Syndrome (FKTN)
    No disease-causing mutations detected
    Fragile X Syndrome (FMR1)
    No disease-causing mutations detected; CGG repeat number within normal range
    Fumarase Deficiency (FH)
    No disease-causing mutations detected
    Galactokinase Deficiency (GALK1)
    No disease-causing mutations detected
    Galactosemia, GALT-Related (GALT)
    No disease-causing mutations detected
    Gaucher Disease (GBA)
    No disease-causing mutations detected
    Gitelman Syndrome (SLC12A3)
    No disease-causing mutations detected
    GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2)
    No disease-causing mutations detected
    Glutaric Acidemia Type 1 (GCDH)
    No disease-causing mutations detected
    Glutaric Acidemia, Type IIa (ETFA)
    No disease-causing mutations detected
    Glutaric Acidemia, Type IIc (ETFDH)
    No disease-causing mutations detected
    Glycine Encephalopathy, AMT-Related (AMT)
    No disease-causing mutations detected
    Glycine Encephalopathy, GLDC-Related (GLDC)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ia (G6PC)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ib (SLC37A4)
    No disease-causing mutations detected
    Glycogen Storage Disease Type III (AGL)
    No disease-causing mutations detected
    Glycogen Storage Disease Type V (PYGM)
    No disease-causing mutations detected
    Glycogen Storage Disease, Type IV also known as Adult Polyglucosan Body Disease (GBE1)
    No disease-causing mutations detected
    Glycogen Storage Disease, Type VII (PFKM)
    No disease-causing mutations detected
    GRACILE Syndrome (BCS1L)
    No disease-causing mutations detected
    Guanidinoacetate Methyltransferase Deficiency also known as Cerebral Creatine Deficiency Syndrome 2 (GAMT)
    No disease-causing mutations detected
    Hemochromatosis, Type 2A (HFE2)
    No disease-causing mutations detected
    Hemochromatosis, Type 3 (TFR2)
    No disease-causing mutations detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing mutations detected
    Hereditary Spastic Paraparesis 49 (TECPR2)
    No disease-causing mutations detected
    Hermansky-Pudlak Syndrome, Type 1 (HPS1)
    No disease-causing mutations detected
    Hermansky-Pudlak Syndrome, Type 3 (HPS3)
    No disease-causing mutations detected
    Holocarboxylase Synthetase Deficiency (HLCS)
    No disease-causing mutations detected
    Homocystinuria (CBS)
    No disease-causing mutations detected
    Homocystinuria due to MTHFR Deficiency (MTHFR)
    No disease-causing mutations detected
    Homocystinuria, Cobalamin E Type (MTRR)
    No disease-causing mutations detected
    Hydrolethalus Syndrome (HYLS1)
    No disease-causing mutations detected
    Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome (SLC25A15)
    No disease-causing mutations detected
    Hypohidrotic Ectodermal Dysplasia, X-Linked (EDA)
    No disease-causing mutations detected
    Hypophosphatasia, Autosomal Recessive (ALPL)
    No disease-causing mutations detected
    Inclusion Body Myopathy 2 (GNE)
    No disease-causing mutations detected
    Isovaleric Acidemia (IVD)
    No disease-causing mutations detected
    Joubert Syndrome 2 (TMEM216)
    No disease-causing mutations detected
    Joubert Syndrome 7 also known as Meckel Syndrome 5 (RPGRIP1L)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMA3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMB3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMC2)
    No disease-causing mutations detected
    Juvenile Retinoschisis, X-Linked (RS1)
    No disease-causing mutations detected
    Krabbe Disease (GALC)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 10 and Other CEP290-Related Ciliopathies (CEP290)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 13 (RDH12)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 2 also known as Retinitis Pigmentosa 20 (RPE65)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 5 (LCA5)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 8 also known as Retinitis Pigmentosa 12 (CRB1)
    No disease-causing mutations detected
    Leigh Syndrome, French-Canadian Type (LRPPRC)
    No disease-causing mutations detected
    Lethal Congenital Contracture Syndrome 1 (GLE1)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2B also known as Dysferlinopathy (DYSF)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2C also known as Gamma-Sarcoglycanopathy (SGCG)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2D also known as Alpha-Sarcoglycanopathy (SGCA)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2E also known as Beta-Sarcoglycanopathy (SGCB)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2I (FKRP)
    No disease-causing mutations detected
    Lipoid Adrenal Hyperplasia (STAR)
    No disease-causing mutations detected
    Lipoprotein Lipase Deficiency (LPL)
    No disease-causing mutations detected
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    No disease-causing mutations detected
    Lysinuric Protein Intolerance (SLC7A7)
    No disease-causing mutations detected
    Lysosomal Acid Lipase Deficiency including Wolman Disease and Cholesteryl Ester Storage Disease (LIPA)
    No disease-causing mutations detected
    Major Histocompatibility Complex Class II Deficiency also known as Bare Lymphocyte Syndrome Type II (CIITA)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 1A (BCKDHA)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 1B (BCKDHB)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing mutations detected
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing mutations detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts Type 1 (MLC1)
    No disease-causing mutations detected
    Menkes Disease and Other ATP7A-Related Disorders, X-Linked (ATP7A)
    No disease-causing mutations detected
    Metachromatic Leukodystrophy (ARSA)
    No disease-causing mutations detected
    Methylmalonic Acidemia (MMAA)
    No disease-causing mutations detected
    Methylmalonic Acidemia (MMAB)
    No disease-causing mutations detected
    Methylmalonic Acidemia (MUT)
    No disease-causing mutations detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin C Type (MMACHC)
    No disease-causing mutations detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin D Type (MMADHC)
    No disease-causing mutations detected
    Microphthalmia and Anophthalmia (VSX2)
    No disease-causing mutations detected
    Mitochondrial Complex I Deficiency (ACAD9)
    No disease-causing mutations detected
    Mitochondrial Complex I Deficiency 16 (NDUFAF5)
    No disease-causing mutations detected
    Mitochondrial Complex I Deficiency, NDUFS6-Related (NDUFS6)
    No disease-causing mutations detected
    Mitochondrial DNA Depletion Syndrome 6 also known as Navajo Neurohepatopathy (MPV17)
    No disease-causing mutations detected
    Mitochondrial Myopathy and Sideroblastic Anemia 1 (PUS1)
    No disease-causing mutations detected
    Mitochondrial Neurogastrointestinal Encephalopathy Disease (TYMP)
    No disease-causing mutations detected
    Mucolipidosis II and IIIA (GNPTAB)
    No disease-causing mutations detected
    Mucolipidosis III Gamma (GNPTG)
    No disease-causing mutations detected
    Mucolipidosis Type IV (MCOLN1)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type I also known as Hurler Syndrome (IDUA)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type II also known as Hunter Syndrome, X-Linked (IDS)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIIA also known as Sanfilippo A Syndrome (SGSH)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIIB also known as Sanfilippo B Syndrome (NAGLU)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIIC also known as Sanfilippo C Syndrome (HGSNAT)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIID (GNS)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IVb also known as GM1 Gangliosidosis (GLB1)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type VI (ARSB)
    No disease-causing mutations detected
    Mucopolysaccharidosistype IX (HYAL1)
    No disease-causing mutations detected
    Multiple Sulphatase Deficiency (SUMF1)
    No disease-causing mutations detected
    Muscle-Eye-Brain Disease (POMGNT1)
    No disease-causing mutations detected
    Myotubular Myopathy, X-Linked (MTM1)
    No disease-causing mutations detected
    N-Acetylglutamate Synthase Deficiency (NAGS)
    No disease-causing mutations detected
    Nemaline Myopathy 2 (NEB)
    No disease-causing mutations detected
    Nephrogenic Diabetes Insipidus, Type II (AQP2)
    No disease-causing mutations detected
    Nephrotic Syndrome, NPHS1-Related also known as Congenital Finnish Nephrosis (NPHS1)
    No disease-causing mutations detected
    Nephrotic Syndrome, NPHS2-Related also known as Steroid-Resistant Nephrotic Syndrome (NPHS2)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN3-Related (CLN3)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN5-Related (CLN5)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN6-Related (CLN6)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN8-Related also known as Northern Epilepsy (CLN8)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, MFSD8-Related (MFSD8)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, PPT1-Related (PPT1)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, TPP1-Related (TPP1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type C, NPC1-Related (NPC1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type C, NPC2-Related (NPC2)
    No disease-causing mutations detected
    Nijmegen Breakage Syndrome (NBN)
    No disease-causing mutations detected
    Oculocutaneous Albinism Type 2 (OCA2)
    No disease-causing mutations detected
    Odonto-Onycho-Dermal Dysplasia also known as Schopf-Schulz-Passarge Syndrome (WNT10A)
    No disease-causing mutations detected
    Omenn Syndrome and Severe Combined Immunodeficiency, Athabaskan-Type (DCLRE1C)
    No disease-causing mutations detected
    Omenn Syndrome, RAG2-Related (RAG2)
    No disease-causing mutations detected
    Ornithine Aminotransferase Deficiency (OAT)
    No disease-causing mutations detected
    Ornithine Transcarbamylase Deficiency, X-Linked (OTC)
    No disease-causing mutations detected
    Osteochondrodysplasias, Sulfate Transporter-Related (SLC26A2)
    No disease-causing mutations detected
    Osteopetrosis Type 1 (TCIRG1)
    No disease-causing mutations detected
    Pendred Syndrome (SLC26A4)
    No disease-causing mutations detected
    Phenylalanine Hydroxylase Deficiency also known as Phenylketonuria (PAH)
    No disease-causing mutations detected
    Polycystic Kidney Disease, Autosomal Recessive (PKHD1)
    No disease-causing mutations detected
    Polyglandular Autoimmune Syndrome Type 1 (AIRE)
    No disease-causing mutations detected
    Pompe Disease also known as Glycogen Storage Disease Type II (GAA)
    No disease-causing mutations detected
    Pontocerebellar Hypoplasia Type 1A (VRK1)
    No disease-causing mutations detected
    Pontocerebellar Hypoplasia Type 6 (RARS2)
    No disease-causing mutations detected
    Postnatal Progressive Microcephaly also known as Infantile Cerebral and Cerebellar Atrophy (MED17)
    No disease-causing mutations detected
    Primary Carnitine Deficiency (SLC22A5)
    No disease-causing mutations detected
    Primary Ciliary Dyskinesia, DNAH5-Related (DNAH5)
    No disease-causing mutations detected
    Primary Ciliary Dyskinesia, DNAI1-Related (DNAI1)
    No disease-causing mutations detected
    Primary Ciliary Dyskinesia, DNAI2-Related (DNAI2)
    No disease-causing mutations detected
    Primary Hyperoxaluria Type 1 (AGXT)
    No disease-causing mutations detected
    Primary Hyperoxaluria Type 2 (GRHPR)
    No disease-causing mutations detected
    Primary Hyperoxaluria, Type 3 (HOGA1)
    No disease-causing mutations detected
    Progressive Cerebello-Cerebral Atrophy (SEPSECS)
    No disease-causing mutations detected
    Progressive Familial Intrahepatic Cholestasis Type 2 (ABCB11)
    No disease-causing mutations detected
    Propionic Acidemia, PCCA-Related (PCCA)
    No disease-causing mutations detected
    Propionic Acidemia, PCCB-Related (PCCB)
    No disease-causing mutations detected
    Pycnodysostosis (CTSK)
    No disease-causing mutations detected
    Pyruvate Dehydrogenase E1-Alpha Deficiency (PDHA1)
    No disease-causing mutations detected
    Pyruvate Dehydrogenase E1-Beta Deficiency (PDHB)
    No disease-causing mutations detected
    Renal Tubular Acidosis and Deafness (ATP6V1B1)
    No disease-causing mutations detected
    Retinitis Pigmentosa 25 (EYS)
    No disease-causing mutations detected
    Retinitis Pigmentosa 26 (CERKL)
    No disease-causing mutations detected
    Retinitis Pigmentosa 28 (FAM161A)
    No disease-causing mutations detected
    Retinitis Pigmentosa 59 (DHDDS)
    No disease-causing mutations detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing mutations detected
    Rhizomelic Chondrodysplasia Punctata Type 3 (AGPS)
    No disease-causing mutations detected
    Roberts Syndrome (ESCO2)
    No disease-causing mutations detected
    Salla Disease (SLC17A5)
    No disease-causing mutations detected
    Sandhoff Disease (HEXB)
    No disease-causing mutations detected
    Schimke Immunoosseous Dysplasia (SMARCAL1)
    No disease-causing mutations detected
    Segawa Syndrome (TH)
    No disease-causing mutations detected
    Severe Combined Immunodeficiency, X-Linked (IL2RG)
    No disease-causing mutations detected
    Sjogren-Larsson Syndrome (ALDH3A2)
    No disease-causing mutations detected
    Smith-Lemli-Opitz Syndrome (DHCR7)
    No disease-causing mutations detected
    Spastic Ataxia of Charlevoix-Saguenay, Autosomal Recessive (SACS)
    No disease-causing mutations detected
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Spondylothoracic Dysostosis (MESP2)
    No disease-causing mutations detected
    Steel Syndrome (COL27A1)
    No disease-causing mutations detected
    Stuve-Wiedemann Syndrome (LIFR)
    No disease-causing mutations detected
    Tay-Sachs Disease also known as Hexosaminidase A Deficiency (HEXA)
    No disease-causing mutations detected; normal enzyme analysis
    TGM1-Related Autosomal Recessive Congenital Ichthyosis (TGM1)
    No disease-causing mutations detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing mutations detected
    Usher Syndrome Type IB (MYO7A)
    No disease-causing mutations detected
    Usher Syndrome Type IC (USH1C)
    No disease-causing mutations detected
    Usher Syndrome Type ID (CDH23)
    No disease-causing mutations detected
    Usher Syndrome Type IF (PCDH15)
    No disease-causing mutations detected
    Usher Syndrome Type IIA (USH2A)
    No disease-causing mutations detected
    Usher Syndrome Type IIIA (CLRN1)
    No disease-causing mutations detected
    Vanishing White Matter Disease (EIF2B5)
    No disease-causing mutations detected
    Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
    No disease-causing mutations detected
    Wilson Disease (ATP7B)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX1-Related (PEX1)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX2-Related (PEX2)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX6-Related (PEX6)
    No disease-causing mutations detected
    Zellweger Syndrome Spectrum, PEX10- Related (PEX10)
    No disease-causing mutations detected
  • Medication Allergy:
    No
    Food Allergy:
    No
    Pet Allergy:
    No
    Hay Fever Allergy:
    No
    Insect Allergy:
    No
    Vaccine Allergy:
    No
    Healthy Teeth:
    Yes
    Braces:
    No
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    No
    Chicken Pox Age:
    Vertigo:
    No
    Comments:
    Donor had a hernia surgically removed at the age of 4.
    Eyesight Correction:
    Yes
    Near or Far Sighted:
    Nearsighted
    Skin Infection:
    No
    Gallstones:
    No
    Removed Gall Bladder:
    No
    Hernia:
    Yes
    Mumps:
    No
    Measles:
    No
    Measles Age:
    German Measles:
    No
    German Measles Age:
    Sinus Infection:
    No
    Stomach Ulcers:
    No

  • Skills, Hobbies and Interests:
    TRAVEL, TEACHING, MOVIES

  • In School:
    Yes
    Is the donor currently enrolled in or does the donor hold an undergraduate degree?
    Yes
    Degree Earned/Working towards:
    BACHELOR OF SCIENCE
    Degree Status:
    Graduated
    Major:
    ECONOMICS
    Minor:
    LAW
    Is the donor currently enrolled in or does the donor hold a graduate degree?
    Yes
    Degree Earned/Working towards:
    MASTER OF SCIENCE
    Degree Status:
    Graduated
    Major:
    FINANCE
    Minor:
    N/A
    Degree Earned/Working towards:
    PHD
    Degree Status:
    Currently enrolled
    Major:
    ECONOMICS
    Minor:
    N/A
    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 Grandfather X 67
    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
    Heart Disease X
    High Blood Pressure X
    High Cholesterol/Triglycerides X
    Stroke X
    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
    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 Disease 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
    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
    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 (Creutzfeld-Jacob 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 - Bronchial Asthma X Grandmother X 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 Grandmother X 36
    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 (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, Dark Eyesight:
    Freckles: Few Hair Texture: Coarse
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 1963 Cause of Death: Hair Loss:
    Height: 5'07" (170.18 cm) Age at Death: Body Hair: Straight
    Weight: 154 lbs. (69 kg) Occupation: IT Engineer Eye Color: Grey
    Half Siblings: No Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Interests are in weightlifting, computers, and reading.
    FAMILY MEMBER: Mother
    Hair Color: Brown, Dark Eyesight:
    Freckles: Few Hair Texture: Fine
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1965 Cause of Death: Hair Loss:
    Height: 5'01" (154.94 cm) Age at Death: Body Hair: Wavy
    Weight: 139 lbs. (63 kg) Occupation: Telecom Engineer; Teacher; Seamstress Eye Color: Brown, Dark
    Half Siblings: No Education: Masters Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She is a speech therapist for kids and a defectologist. Enjoys sewing, reading, and gardening.
    FAMILY MEMBER: Son
    Hair Color: Blonde, Dark Eyesight:
    Freckles: None Hair Texture: Fine
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 2017 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair: Straight
    Weight: 033 lbs. (14 kg) Occupation: Eye Color: Brown, Dark
    Half Siblings: No Education: Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He is bilingual, has an excellent memory, and is very sociable. Enjoys running, impersonating animals, and playing with dogs.

  • 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: Black Eyesight:
    Freckles: None Hair Texture: Fine
    Health Status: Fair Skin Tone: Olive Dominant Hand:
    Year of Birth: 1937 Cause of Death: Hair Loss:
    Height: 5'09" (175.26 cm) Age at Death: Body Hair: Straight
    Weight: 150 lbs. (68 kg) Occupation: Telecommunications Engineer-Supervisor Eye Color: Grey
    Half Siblings: Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Interests are in radio technology and reading.
    FAMILY MEMBER: Grandmother
    Hair Color: Blonde, Medium Eyesight:
    Freckles: None Hair Texture: Thin
    Health Status: Fair Skin Tone: Fair Dominant Hand:
    Year of Birth: 1941 Cause of Death: Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: Body Hair: Straight
    Weight: 169 lbs. (76 kg) Occupation: Telecommunications Engineer Eye Color: Grey
    Half Siblings: Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoys phone talks and reading.

  • 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, Dark Eyesight:
    Freckles: None Hair Texture:
    Health Status: Skin Tone: Medium Dominant Hand:
    Year of Birth: 1926 Cause of Death: LUNG CANCER Hair Loss:
    Height: 5'05" (165.1 cm) Age at Death: 68 Body Hair: Wavy
    Weight: 154 lbs. (69 kg) Occupation: Driver, Shoemaker Eye Color: Brown, Dark
    Half Siblings: Education: GED Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoyed reading and gardening.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Light Eyesight:
    Freckles: Numerous Hair Texture: Fine
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1931 Cause of Death: BRONCHIAL ASTHMA Hair Loss:
    Height: 5'" (152.4 cm) Age at Death: 51 Body Hair: Straight
    Weight: 143 lbs. (64 kg) Occupation: Road Technician Eye Color: Green
    Half Siblings: Education: GED Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoyed sewing and knitting.
    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:
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1963 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:
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Fair Skin Tone: Dominant Hand:
    Year of Birth: 1957 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 #5607

All prices shown are in USD.

$1350 per vial Identity Disclosure xyGene Washed

$1350 per vial Identity Disclosure xyGene Unwashed

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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