fbpx

Donor Profile : Donor 5533

of Profiles
 in your search results

Donor ID: 5533

Save to Favorites

View Donor Photos

Xytex offers you the opportunity to not only view your sperm donor online, but to also purchase his photos.

  • Share donor prints with friends to help you decide
  • Print & keep images in your portfolio to share with your child later

*Due to HFEA Regulations, UK Clients are unable to purchase photos at this time.

Available in various formats, sizes and platforms.

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.

Sign in or Create an Account to view Enhanced Profile

Donor's "Name": Zane

Year of Birth: 1981

Marital Status: Single

Number of Children: 1

Religion: None

Occupation: Renewal Specialist

Blood Type: AB -

Nationality:
(self reported)
Maternal: French
Paternal: English

Race: White Or Caucasian

CMV Status: POS
Learn More

Last Medical History Update: 09/23/2019

  • Reported Pregnancy/Birth
  • xyIdentity Disclosure
  • Available Inventory
ORDER NOW

ADDITIONAL DONOR DETAILS

  • Height:
    6'2" (187.96 cm)
    Weight:
    178 lbs (80 kg)
    Eye Color:
    Blue
    Hair Color:
    Brown
    Hair Texture:
    Average
    Hair Loss:
    None
    Hair Type:
    Average
    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 5533 was tested, including the condition(s) of which he is a carrier. To purchase units from this donor the 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 Video and 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 171 conditions.

    Congenital Disorder of Glycosylation, Type Ic (ALG6)
    Carrier
    Galactosemia, GALT-Related (GALT)
    Carrier of Duarte variant
    11-Beta-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP11B1)
    No disease-causing mutations detected
    21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
    No disease-causing mutations detected
    3-Methylglutaconic Aciduria, Type III also known as Costeff Optic Atrophy Syndrome (OPA3)
    No disease-causing mutations detected
    6-Pyruvoyl-Tetrahydropterin Synthase Deficiency (PTS)
    No disease-causing mutations detected
    Adenosine Deaminase Deficiency (ADA)
    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
    Alport Syndrome, COL4A3-Related (COL4A3)
    No disease-causing mutations detected
    Alport Syndrome, COL4A4-Related (COL4A4)
    No disease-causing mutations detected
    Alstrom Syndrome (ALMS1)
    No disease-causing mutations detected
    Andermann Syndrome (SLC12A6)
    No disease-causing mutations detected
    Argininemia (ARG1)
    No disease-causing mutations detected
    Argininosuccinic Aciduria (ASL)
    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
    ATP7A-Related Disorders, X-Linked (ATP7A)
    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
    Beta-Thalassemia, Sickle Cell Disease, Beta-Globin-Related Hemoglobinopathies (HBB)
    No disease-causing mutations detected; normal red blood cell indices and hemoglobin analysis
    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
    Cartilage-Hair Hypoplasia (RMRP)
    No disease-causing mutations detected
    Cerebrotendinous Xanthomatosis (CYP27A1)
    No disease-causing mutations detected
    Chromosomal Analysis
    Normal male karyotype
    Citrullinemia Type 1 (ASS1)
    No disease-causing mutations detected
    Cohen Syndrome (VPS13B)
    No disease-causing mutations detected
    Combined Pituitary Hormone Deficiency 2 (PROP1)
    No disease-causing mutations detected
    Congenital Amegakaryocytic Thrombocytopenia (MPL)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1a (PMM2)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1b (MPI)
    No disease-causing mutations detected
    Cystic Fibrosis (CFTR)
    No disease-causing mutations detected
    Cystinosis (CTNS)
    No disease-causing mutations detected
    D-Bifunctional Protein Deficiency (HSD17B4)
    No disease-causing mutations detected
    Delta-Sarcoglycanopathy (SGCD)
    No disease-causing mutations detected
    Dyskeratosis Congenita, RTEL1-Related (RTEL1)
    No disease-causing mutations detected
    Dystrophinopathies, X-Linked (DMD)
    No disease-causing mutations detected
    Ellis-Van Creveld Syndrome, EVC-Related (EVC)
    No disease-causing mutations detected
    Ellis-Van Creveld Syndrome, EVC2-Related (EVC2)
    No disease-causing mutations detected
    ERCC6-Related Disorders (ERCC6)
    No disease-causing mutations detected
    ERCC8-Related Disorders (ERCC8)
    No disease-causing mutations detected
    Fabry Disease, X-Linked (GLA)
    No disease-causing mutations detected
    Familial Dysautonomia (IKBKAP)
    No disease-causing mutations detected
    Familial Hyperinsulinism, ABCC8-Related (ABCC8)
    No disease-causing mutations detected
    Familial Hyperinsulinism, KCNJ11-Related (KCNJ11)
    No disease-causing mutations detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing mutations detected
    Fanconi Anemia Group A (FANCA)
    No disease-causing mutations detected
    Fanconi Anemia Group C (FANCC)
    No disease-causing mutations detected
    Galactokinase Deficiency (GALK1)
    No disease-causing mutations detected
    Gaucher Disease (GBA)
    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
    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
    GRACILE Syndrome (BCS1L)
    No disease-causing mutations detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing mutations detected
    HMG-CoA Lyase Deficiency (HMGCL)
    No disease-causing mutations detected
    Holocarboxylase Synthetase Deficiency (HLCS)
    No disease-causing mutations detected
    Homocystinuria, CBS-Related (CBS)
    No disease-causing mutations detected
    Hydrolethalus Syndrome (HYLS1)
    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
    Junctional Epidermolysis Bullosa, LAMA3-Related (LAMA3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa, LAMB3-Related (LAMB3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa, LAMC2-Related (LAMC2)
    No disease-causing mutations detected
    Krabbe Disease (GALC)
    No disease-causing mutations detected
    Leigh Syndrome, French-Canadian Type (LRPPRC)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2A also known as Calpainopathy (CAPN3)
    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
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    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 Lipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing mutations detected
    Maple Syrup Urine Disease, Type II (DBT)
    No disease-causing mutations detected
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing mutations detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts (MLC1)
    No disease-causing mutations detected
    Merosin-Deficient Muscular Dystrophy (LAMA2)
    No disease-causing mutations detected
    Metachromatic Leukodystrophy (ARSA)
    No disease-causing mutations detected
    Methylmalonic Acidemia, MMAA-Related (MMAA)
    No disease-causing mutations detected
    Methylmalonic Acidemia, MMAB-Related (MMAB)
    No disease-causing mutations detected
    Methylmalonic Acidemia, MUT-Related (MUT)
    No disease-causing mutations detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin C Type (MMACHC)
    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 IVb also known as GM1 Gangliosidosis (GLB1)
    No disease-causing mutations detected
    Mucopolysaccharidosis, Type II, X-Linked (IDS)
    No disease-causing mutations detected
    Mucopolysaccharidosis, Type IIIA (SGSH)
    No disease-causing mutations detected
    Mucopolysaccharidosis, Type IIIB (NAGLU)
    No disease-causing mutations detected
    Mucopolysaccharidosis, Type IIIC (HGSNAT)
    No disease-causing mutations detected
    Muscle-Eye-Brain Disease (POMGNT1)
    No disease-causing mutations detected
    Nemaline Myopathy 2 (NEB)
    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, PPT1-Related (PPT1)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, TPP1-Related (TPP1)
    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
    Niemann-Pick Disease, SMPD1-Related (SMPD1)
    No disease-causing mutations detected
    Nijmegen Breakage Syndrome (NBN)
    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
    Peroxisome Biogenesis Disorder, Type 3 (PEX12)
    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
    Primary Carnitine Deficiency (SLC22A5)
    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
    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 Carboxylase Deficiency (PC)
    No disease-causing mutations detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing mutations detected
    Salla Disease (SLC17A5)
    No disease-causing mutations detected
    Sandhoff Disease (HEXB)
    No disease-causing mutations detected
    Segawa Syndrome (TH)
    No disease-causing mutations detected
    Short Chain Acyl-CoA Dehydrogenase Deficiency (ACADS)
    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
    Spastic Paraplegia, Type 15 (ZFYVE26)
    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
    Tay-Sachs Disease (HEXA)
    No disease-causing mutations detected
    TGM1-Related Autosomal Recessive Congenital Ichthyosis (TGM1)
    No disease-causing mutations detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing mutations detected
    Tyrosinemia, Type II (TAT)
    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 IF (PCDH15)
    No disease-causing mutations detected
    Usher Syndrome Type IIA (USH2A)
    No disease-causing mutations detected
    Usher Syndrome Type III (CLRN1)
    No disease-causing mutations detected
    Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
    No disease-causing mutations detected
    Walker-Warburg Syndrome, FKTN-Related (FKTN)
    No disease-causing mutations detected
    Wilson Disease (ATP7B)
    No disease-causing mutations detected
    Wolman Disease also known as Cholesteryl Ester Storage Disease (LIPA)
    No disease-causing mutations detected
    Xeroderma Pigmentosum, Group A (XPA)
    No disease-causing mutations detected
    Xeroderma Pigmentosum, Group C (XPC)
    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 Syndrome Spectrum, PEX10- Related (PEX10)
    No disease-causing mutations detected
    Zellweger Syndrome Spectrum, PEX6-Related (PEX6)
    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:
    Yes
    Chicken Pox Age:
    7
    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 Interest:
    Playing sports, exercise

  • In School:
    No
    Is the donor currently enrolled in or does the donor hold an undergraduate degree?
    No
    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.)?
    Yes
    Type Of Training:
    Military police
    Training Body:
    Military
    Certificate(s) Earned:
    Training course certificate
  • 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
    Sjorgen'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
    VonWillebrand'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
    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 (Crohns) 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 Grandfather X 61
    Kidney disease of 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
    Acondroplasia (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/ Aspergers 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's) 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 (Neurofibrimatosis) X
    Neurologic (Parkinson's Disease) X
    Neurologic (Subacute Sclerosing Panencephalitis) X
    Nieman-Pick X
    Spongioform 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
    Other - Early Death X
    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 (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: Brown, Dark Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 1958 Cause of Death: Hair Loss: Receding
    Height: 5'11" (180.34 cm) Age at Death: Body Hair: Straight
    Weight: 220 lbs. (99 kg) Occupation: Logistics & Distribution Eye Color: Blue
    Half Siblings: No Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has full lips and a strong brow line. He is Mr. Fix-it, mechanically inclined, and a hard worker. Enjoys golf, college football, and his grandchildren.
    FAMILY MEMBER: Mother
    Hair Color: Blonde, Strawberry Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1961 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair: Straight
    Weight: 150 lbs. (68 kg) Occupation: Retired Accountant Eye Color: Blue
    Half Siblings: No Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples (when she smiles) and high cheek bones. She’s a pastry chef who is generous and hardworking. Enjoys crafts.
    FAMILY MEMBER: Son
    Hair Color: Brown, Medium Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 2005 Cause of Death: Hair Loss:
    Height: 4'10" (147.32 cm) Age at Death: Body Hair: Straight
    Weight: 85 lbs. (38 kg) Occupation: Eye Color: Blue
    Half Siblings: No Education: Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples. He’s polite and quiet. Enjoys basketball.
    FAMILY MEMBER: Brother
    Hair Color: Red, Dark Eyesight:
    Freckles: Numerous Hair Texture: Thick
    Health Status: Fair Skin Tone: Fair Dominant Hand:
    Year of Birth: 1984 Cause of Death: Hair Loss:
    Height: 5'09" (175.26 cm) Age at Death: Body Hair: Straight
    Weight: 185 lbs. (83 kg) Occupation: Sales Eye Color: Blue
    Half Siblings: Yes Education: Body Build: Medium
    Half Siblings Parent: Mother Eyesight Correction: Near or Far Sighted:
    Comments: Enjoys cooking.
    FAMILY MEMBER: Sister
    Hair Color: Brown, Medium Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1990 Cause of Death: Hair Loss:
    Height: 5'07" (170.18 cm) Age at Death: Body Hair: Straight
    Weight: 150 lbs. (68 kg) Occupation: Construction Management Eye Color: Blue
    Half Siblings: Yes Education: College (Some) Body Build: Medium
    Half Siblings Parent: Mother Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples. She was a county Spelling Bee champion when she was younger. Enjoys music, friends, and family.
    FAMILY MEMBER: Brother
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1989 Cause of Death: Hair Loss:
    Height: 6'02" (187.96 cm) Age at Death: Body Hair: Straight
    Weight: 200 lbs. (90 kg) Occupation: Police Officer Eye Color: Blue
    Half Siblings: Yes Education: High School Body Build: Medium
    Half Siblings Parent: Father Eyesight Correction: Near or Far Sighted:
    Comments: He’s athletic with a strong brow line. Enjoys golf, sports, and volunteering.
    FAMILY MEMBER: Sister
    Hair Color: Brown, Medium Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1986 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair: Straight
    Weight: 145 lbs. (65 kg) Occupation: Teacher Eye Color: Blue
    Half Siblings: Yes Education: College Body Build: Medium
    Half Siblings Parent: Father Eyesight Correction: Near or Far Sighted:
    Comments: She has compassion and leadership skills. She’s won multiple beauty pageants.
  • 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: Thick
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1931 Cause of Death: Kidney Hair Loss:
    Height: 6'" (182.88 cm) Age at Death: 61 Body Hair: Wavy
    Weight: 190 lbs. (86 kg) Occupation: Barber Eye Color: Hazel/Blue
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Served in WWII. Enjoyed history and gem stones.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Light Eyesight:
    Freckles: Few Hair Texture: Thick
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1937 Cause of Death: Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: Body Hair: Straight
    Weight: 160 lbs. (72 kg) Occupation: Board of Education Eye Color: Blue
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples and high cheekbones. She’s a pastry chef. Enjoys church/religion, gems & mining.
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1960 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: Good Skin Tone: Dominant Hand:
    Year of Birth: 1958 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: Skin Tone: Dominant Hand:
    Year of Birth: 1955 Cause of Death: Natural 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, Dark Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 1942 Cause of Death: Hair Loss:
    Height: 5'11" (180.34 cm) Age at Death: Body Hair: Straight
    Weight: 175 lbs. (79 kg) Occupation: Real Estate Broker Eye Color: Blue
    Half Siblings: Education: College (Some) Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has a distinctive jaw line. Received multiple awards including real estate awards. Enjoys ballroom dancing, music, and farming.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Fair Skin Tone: Medium Dominant Hand:
    Year of Birth: 1939 Cause of Death: Hair Loss:
    Height: 5'01" (154.94 cm) Age at Death: Body Hair: Straight
    Weight: 115 lbs. (52 kg) Occupation: Housekeeper Eye Color: Hazel/Blue
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has high cheekbones. She kept up/keeps up with technology well into her ‘old-age’. Enjoys cooking, animals, and grandchildren.
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1970 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: 1966 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: 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

Unit Types Available for Donor #5533

All prices shown are in USD.

$1195 per unit Identity Disclosure xyGene Washed

$1195 per unit Identity Disclosure xyGene Unwashed

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

Ready to Order Units?

Click the button below to order online.
ORDER NOW

Need personalized help with your order?

Monday - Friday, 9 a.m. - 5 p.m. EST (excludes USA holidays)

Online Ordering Disclaimer:
Purchasing units 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.