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Donor Profile : Donor 5426

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Donor ID: 5426

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Meet The Donor

It's quite an accomplishment to obtain Eagle Scout status, and Donor 5426 knows it. He also draws and plays piano and guitar, in addition to attending a prestigious engineering school. He loves storytelling and the emotions and memories a good story will invoke.

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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.

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Donor's "Name": Clay

Year of Birth: 1992

Marital Status: Single

Number of Children: 0

Religion: Christian

Occupation: Student

Blood Type: O +

Nationality:
(self reported)
Maternal: English
Scottish
Indigenous American
Paternal: English
Scottish
Indigenous American

Race: White Or Caucasian

CMV Status: POS
Learn More

Last Medical History Update: 05/07/2020

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

  • Height:
    5'7" (170.18 cm)
    Weight:
    140 lbs (63 kg)
    Eye Color:
    Blue/Grey
    Hair Color:
    Blonde, Dark
    Hair Texture:
    Fine
    Hair Loss:
    None
    Hair Type:
    Average
    Dominant Hand:
    Right
    Hairy Chest:
    No
    Hairy:
    Yes
    Ear Lobes:
    Attached
    Beard Color:
    Blonde, Dark
    Eyebrows:
    Medium
    Dimples:
    No
    Acne:
    Yes
    Acne Information:
    Shoe Size:
    7 1/2
    Body Build:
    Small
    Freckles:
    Few
    Skin Tone:
    Fair
    Face Shape:
    Oval
    Lips:
    Normal
    Nose Shape:
    Normal
    Long Eyelashes:
    No
  • Since an early age, I’ve loved adventure and the outdoors. I was a Boy Scout for 7 years and attained the highest honor of Eagle Scout. I’ve played all kinds of sports ranging from Boxing, to Archery, to Cheerleading. I ran varsity cross country in high school, as well as being involved in musical theater.
    While writing this to you, I’m a first-generation college student studying computer science at a top ranked engineering school. I’ve paid for almost my entire college education by myself without taking a single cent out in loans. I’m a member of a social fraternity on campus, and am also a D1 scholarship athlete. I have a wide variety of talents I’ve picked up over the years such as whistling, welding, making sushi, speaking Japanese, and juggling.
    My family members tend to live for a long time, in fact my grandmother is turning 94 this year. My family shows tendency towards creativity and intelligence, my father designs circuits and electronics that are being put into the International Space Station. His brother runs his own dentistry clinic, and their father was head of a federal banking chain during the middle of the 20th century. My great grandfather ran the largest chicken hatchery in the entire southeast, something he built from the ground up. My grandmother is not only an accomplished artist, but also a published writer.
    I’ve got a passion for telling stories. Writing, speaking, the medium doesn’t matter. The thing that matters to me is seeing the other person enjoy the experience. Stories are pieces of our legacy. They’re part of what we leave behind. They can be trivial, or they can be defining moments showing a glimpse of who we were and who we will become. Fiction or not, stories connect people and I love sharing them.
    Before I end this letter, I just hope that reading this has helped you in some way. Even if only a little bit. Make sure that you live your life in a way that makes you and others happy. Good luck!

    Sincerely,
    Donor 5426

  • 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 106 conditions.

    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
    Achromatopsia (CNGB3)
    No disease-causing mutations detected
    Alkaptonuria (HGD)
    No disease-causing mutations detected
    Alpha-1 Antitrypsin Deficiency (SERPINA1)
    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
    Andermann Syndrome (SLC12A6)
    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, BBS1-Related (BBS1)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS10-Related (BBS10)
    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
    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
    Choroidemia (CHM)
    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 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
    Factor XI Deficiency (F11)
    No disease-causing mutations detected
    Familial Dysautonomia (IKBKAP)
    No disease-causing mutations detected
    Familial Hyperinsulinism, ABCC8-Related (ABCC8)
    No disease-causing mutations detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing mutations detected
    Fanconi Anemia Group C (FANCC)
    No disease-causing mutations detected
    Galactosemia, GALT-Related (GALT)
    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
    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
    GRACILE Syndrome (BCS1L)
    No disease-causing mutations detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing mutations detected
    Hereditary Thymine-Uraciluria also known as Dihydropyrimidine Dehydrogenase Deficiency (DPYD)
    No disease-causing mutations detected
    Homocystinuria, CBS-Related (CBS)
    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
    Juvenile Retinoschisis, X-Linked (RS1)
    No disease-causing mutations detected
    Krabbe Disease (GALC)
    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
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    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
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing mutations detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts (MLC1)
    No disease-causing mutations detected
    Metachromatic Leukodystrophy (ARSA)
    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
    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, 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, SMPD1-Related (SMPD1)
    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
    Osteochondrodysplasias, Sulfate Transporter-Related (SLC26A2)
    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
    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
    Pseudocholinesterase Deficiency (BCHE)
    No disease-causing mutations detected
    Pycnodysostosis (CTSK)
    No disease-causing mutations detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing mutations detected
    Salla Disease (SLC17A5)
    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
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Steroid-Resistant Nephrotic Syndrome
    See results for Nephrotic Syndrome, NPHS2-Related (NPHS2)
    Tay-Sachs Disease (HEXA)
    No disease-causing mutations detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing mutations detected
    Usher Syndrome Type IF (PCDH15)
    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
    Wilson Disease (ATP7B)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX1-Related (PEX1)
    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:
    Yes
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    No
    Chicken Pox Age:
    Vertigo:
    No
    Eyesight Correction:
    Yes
    Near or Far Sighted:
    Nearsighted
    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:
    Yes
    Stomach Ulcers:
    No
  • ATHLETIC

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    • 4
    • 5

    COUCH POTATO

    OPTIMISTIC

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    • 3
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    PESSIMISTIC

    ASSERTIVE

    • 1
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    • 3
    • 4
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    PASSIVE

    LEADER

    • 1
    • 2
    • 3
    • 4
    • 5

    FOLLOWER

    EASY GOING

    • 1
    • 2
    • 3
    • 4
    • 5

    CONTROLLING, RIGID

    ARTISTIC

    • 1
    • 2
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    MICHELANGELO WHO?

    EXTROVERT

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    INTROVERT

    Celebrity Look Alike:

    Vegetarian: No

    Adjectives: Silly, Loyal, Friendly

    Fine Art Skills: Music (piano & guitar) and drawing

    Technical/Mechanical Ability: I can weld, fix plumbing and/or electrical problems, and set a timer on a VCR.

    Skills, Hobbies and Interest: I can whistle, weld metal together, roll sushi, and hold my breath for over a minute. I run long distance for exercise and am also a GT scholarship athlete for cheerleader.

  • Carried to Term:
    No
    Pregnancy Complications:
    No
    Birth Weight:
    6 lbs ounces
    Childhood Health:
    Excellent
    Birth Length:
    16 inches
    Twin:
    No
    Twin Type:
    In School:
    Yes
    In School Major:
    Computer science
    Post Graduate:
    No
    Training Type:
    College Degrees:
    none
  • 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 Grandfather X 94
    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
    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 Grandmother X 77
    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 Mother X 56
    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 Grandfather X 28
    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) Gluten X Mother X 54
    Allergies (Hay Fever) X
    Allergies (Insect) X
    Allergies (Other) X
    Allergies (Pet) Cats X Mother X 34
    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 Grandfather X 89
    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: Black Eyesight:
    Freckles: Numerous Hair Texture: Thick
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1949 Cause of Death: Hair Loss: Extensive Balding
    Height: 5'09" (175.26 cm) Age at Death: Body Hair: Straight
    Weight: 170 lbs. (77 kg) Occupation: Electrical Engineer Eye Color: Brown, Dark
    Half Siblings: No Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He used to be a rock star; he’s a lead guitar player and pilot. Enjoys cars, computers, cycling, football, model and regular: planes and trains, and guns.
    FAMILY MEMBER: Mother
    Hair Color: Blonde, Dark Eyesight:
    Freckles: Few Hair Texture: Thin
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1955 Cause of Death: Hair Loss:
    Height: 5'02" (157.48 cm) Age at Death: Body Hair: Straight
    Weight: 130 lbs. (59 kg) Occupation: Accountant Eye Color: Brown, Dark
    Half Siblings: No Education: Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has correct vision. She has two green thumbs! Enjoys cooking, filing taxes, accounting, marketing, gardening and sewing.
  • 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: Blonde, Strawberry Eyesight:
    Freckles: Numerous Hair Texture: Thin
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1919 Cause of Death: Old age Hair Loss: Extensive Balding
    Height: 5'08" (172.72 cm) Age at Death: 96 Body Hair: Straight
    Weight: 160 lbs. (72 kg) Occupation: Bank CEO Eye Color: Blue
    Half Siblings: Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision. Enjoyed farming, sailing/boating, cooking, and RC airplanes.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Medium Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Fair Skin Tone: Fair Dominant Hand:
    Year of Birth: 1924 Cause of Death: Hair Loss:
    Height: 5'03" (160.02 cm) Age at Death: Body Hair: Curly
    Weight: 120 lbs. (54 kg) Occupation: School Teacher Eye Color: Brown, Light
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Enjoys painting, drawing, writing (published).
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1952 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: 1955 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: Black Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Fair Skin Tone: Medium Dominant Hand:
    Year of Birth: 1922 Cause of Death: Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Straight
    Weight: 180 lbs. (81 kg) Occupation: Eye Color: Brown, Dark
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture: Thin
    Health Status: Fair Skin Tone: Fair Dominant Hand:
    Year of Birth: 1928 Cause of Death: Hair Loss:
    Height: 5'" (152.4 cm) Age at Death: Body Hair: Curly
    Weight: 110 lbs. (49 kg) Occupation: School Teacher Eye Color: Brown, Light
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Enjoys gardening, knitting, crocheting, and sewing.
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1961 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: 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:
    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:
Buy one get one 1/2 off on this featured donor

Purchase Bundle Options

Purchase Bundle Options

Unit Types Available for Donor #5426

All prices shown are in USD.

$1195 per unit Identity Disclosure xyGene Washed

$1195 per unit Identity Disclosure xyGene Unwashed

$650 per unit Identity Disclosure xyGene ART

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

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