Donor Profile : Donor 40013

of Profiles
 in your search results
Buy one get one 1/2 off on this featured donor

Donor ID: 40013

Save to Favorites

Meet The Donor

Donor 40013 is extremely intelligent, and started his own business. He tested out 4-5 before finding a successful formula. He loves dogs, especially large breeds. His true passion - and one he hopes everyone enjoys - is music. He's a talented guitarist but excels at songwriting. He's athletic and assertive but music keeps him in touch with his softer side.

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": Dylan

Year of Birth: 1990

Marital Status: Married

Number of Children: 0

Religion: Agnostic

Occupation:
(last reported)
Business Owner

Blood Type: A +

Nationality:
(self reported)
Maternal: Irish
Paternal: German

Race: White Or Caucasian

CMV Status: POS
Learn More

Last Medical History Update: 08/17/2020

  • Reported Pregnancy/Birth
  • xyIdentity Disclosure
  • Available Inventory
Download PDF Profile ORDER NOW

ADDITIONAL DONOR DETAILS

  • Height:
    5'10" (177.8 cm)
    Weight:
    155 lbs (70 kg)
    Eye Color:
    Hazel/Green
    Hair Color:
    Brown, Dark
    Hair Texture:
    Fine
    Hair Loss:
    None
    Hair Type:
    Straight
    Dominant Hand:
    Right
    Hairy Chest:
    Yes
    Hairy:
    Yes
    Ear Lobes:
    Detached
    Beard Color:
    Black
    Eyebrows:
    Medium
    Dimples:
    Yes
    Acne:
    No
    Acne Information:
    Shoe Size:
    10
    Body Build:
    Medium
    Freckles:
    Few
    Skin Tone:
    Medium
    Face Shape:
    Oval
    Lips:
    Normal
    Nose Shape:
    Normal
    Long Eyelashes:
    No
  • It’s a hard thing to do—to fill a page with the culmination of your experience in life thus far. Where do you draw the line between extraneous and essential? How can I know what will be important for you to know? I guess the best I can hope to do is to provide you with some context to those feelings in your gut, those underlying attractions or dislikes that you can’t seem to put your finger on. Let’s get into it.
    I’m the youngest of three kids from two amazing parents. My father is smart, innovative, and highly successful. My mother is beautiful, kind, and as sweet as can be. My sister is a firecracker. She’s witty, sharp, but also very gentle and motherly with three kids of her own. My brother is an incredible violinist and a genius when it comes to computers and technology— he taught himself to code at the age of 13. Defying all the odds, I was somehow born exceedingly athletic. I switched between baseball and soccer as a kid, but quickly realized my strengths were on the soccer pitch. Although the family itself is kind of a mixed bag, we all share one thing in common— a gift for music. My father and I play guitar, my sister sings, my brother plays violin and mandolin, and my mother grew up on the piano bench. If you haven’t yet, give it go. Writing songs has always helped me get through hard times.
    I don’t know if this is something you’ll relate to, but I love dogs. I grew up with a beagle, then a golden retriever. Now as an adult, I have a Saint Bernard, Newfoundland, and a German Shepherd. There’s no friend more dependable than a good dog.
    If you’re anything like me, you’ll be filled with entrepreneurial aspirations. Don’t be afraid to try that side of you out. I got that from my father, and I hope I can pass that down to you. My first 4 or 5 businesses either flopped or floundered, but I kept going and moderate success followed and made way for bigger and bigger opportunities.
    This is the part where I pass on some advice. Don’t get this confused with me thinking I know what’s best for you. The only person who knows that for certain is you. These are just a few rules I live by that work well for me.


    1) Everything in moderation. Don’t get too caught up in one thing. Even something good can turn toxic when overused.
    2) Don’t be afraid of growth. You should be constantly pushing yourself, stretching your limits, and pulling at your boundaries. Love every version of yourself but strive to improve. You’ll be wrong a lot. Learn to accept that. It’s the acceptance of your shortcomings that will allow you to make adjustments and legitimately grow. This holds true in your relationships, your education, your career, you name it.
    3) Read Self-Reliance by Ralph Waldo Emerson then read it again. It’s a great essay with some really amazing perspective on how to cultivate a really strong and secure sense of yourself. It can get a little intense, but just ignore those parts. I try to read it once a year to keep me on track and feeling like there’s nothing, I can’t accomplish.
    4) Be loyal. The world needs more loyalty. Be a rock amongst your friends and family. Always do right by them.

    The best I could hope is that you find happiness. I wish I could tell you where to look, but it’s different for everyone. Live with humility, be the best you, and one day it will be yours.

    Sincerely,
    Donor 40013

  • ADVISORY

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

    Below is a list of all conditions for which donor 40013 was tested, including the condition(s) of which he is a carrier. To purchase units 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 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 177 conditions.
       Download Evaluation Summary

    Galactosemia, GALT-Related (GALT)
    Carrier of Duarte variant
    GRACILE Syndrome (BCS1L)
    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-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
    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
    Arginase Deficiency also known as Argininemia (ARG1)
    No disease-causing mutations detected
    Argininosuccinic Aciduria (ASL)
    No disease-causing mutations detected
    Arthrogryposis, Mental Retardation, and Seizures (AMRS)
    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
    Beta-Thalassemia, Sickle Cell Disease, and Beta-Globin Disorders (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
    Cockayne Syndrome Type A (ERCC8)
    No disease-causing mutations detected
    Cockayne Syndrome Type B (ERCC6)
    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 Adrenal Hyperplasia due to 11-Beta-Hydroxylase Deficiency (CYP11B1)
    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
    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
    Delta-Sarcoglycanopathy (SGCD)
    No disease-causing mutations detected
    Dyskeratosis Congenita, RTEL1-Related (RTEL1)
    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
    Ellis-Van Creveld Syndrome, EVC2-Related (EVC2)
    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 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
    FKTN-Related Disorders including Walker-Warburg Syndrome (FKTN)
    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
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing mutations detected
    Holocarboxylase Synthetase Deficiency (HLCS)
    No disease-causing mutations detected
    Homocystinuria (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)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMB3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (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
    Lysosomal Acid Lipase Deficiency including Wolman Disease and Cholesteryl Ester Storage Disease (LIPA)
    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 2 (DBT)
    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
    Merosin-Deficient Muscular Dystrophy (LAMA2)
    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
    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 IVb also known as GM1 Gangliosidosis (GLB1)
    No disease-causing mutations detected
    Multiple Sulphatase Deficiency (SUMF1)
    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 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
    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
    Retinitis Pigmentosa 59 (DHDDS)
    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 also known as Hexosaminidase A Deficiency (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 IIIA (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
    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 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:
    Yes
    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
  • ATHLETIC

    • 1
    • 2
    • 3
    • 4
    • 5

    COUCH POTATO

    OPTIMISTIC

    • 1
    • 2
    • 3
    • 4
    • 5

    PESSIMISTIC

    ASSERTIVE

    • 1
    • 2
    • 3
    • 4
    • 5

    PASSIVE

    LEADER

    • 1
    • 2
    • 3
    • 4
    • 5

    FOLLOWER

    EASY GOING

    • 1
    • 2
    • 3
    • 4
    • 5

    CONTROLLING, RIGID

    ARTISTIC

    • 1
    • 2
    • 3
    • 4
    • 5

    MICHELANGELO WHO?

    EXTROVERT

    • 1
    • 2
    • 3
    • 4
    • 5

    INTROVERT

    Celebrity Look Alike: Justin Long-Actor

    Vegetarian: No

    Adjectives: Confident, Loyal, Empathetic

    Fine Art Skills: Music: guitar and songwriting

    Technical/Mechanical Ability: Moderate handyman skills

    Skills, Hobbies and Interests:

  • Carried to Term:
    Yes
    Pregnancy Complications:
    No
    Birth Weight:
    8 lbs ounces
    Childhood Health:
    Excellent
    Birth Length:
    20 inches
    Twin:
    No
    Twin Type:
    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.)?
    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
    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 Grandfather X 45
    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
    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 Grandfather X 45
    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) Cat X Mother 15
    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: Blonde, Medium Eyesight:
    Freckles: None Hair Texture: Fine
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 1960 Cause of Death: Hair Loss:
    Height: 6'" (182.88 cm) Age at Death: Body Hair:
    Weight: 175 lbs. (79 kg) Occupation: CEO-Tech Company Eye Color: Brown, Light
    Half Siblings: No Education: Masters Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has correct vision. He’s a German major. Enjoys fitness (running and swimming).
    FAMILY MEMBER: Mother
    Hair Color: Auburn Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 1959 Cause of Death: Hair Loss:
    Height: 5'04" (162.56 cm) Age at Death: Body Hair: Wavy
    Weight: 130 lbs. (59 kg) Occupation: Small Business Owner-Textiles Eye Color: Hazel/Green
    Half Siblings: No Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision and dimples. She’s active in the non-profit world and volunteers for everything. Enjoys piano and quilting.
    FAMILY MEMBER: Sister
    Hair Color: Blonde, Medium Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1987 Cause of Death: Hair Loss:
    Height: 5'09" (175.26 cm) Age at Death: Body Hair: Straight
    Weight: 140 lbs. (63 kg) Occupation: Teacher Eye Color: Blue/Green
    Half Siblings: No Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Started an interior design company.
    FAMILY MEMBER: Brother
    Hair Color: Blonde, Medium Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1989 Cause of Death: Hair Loss:
    Height: 5'09" (175.26 cm) Age at Death: Body Hair:
    Weight: 170 lbs. (77 kg) Occupation: Musician Eye Color: Hazel/Blue
    Half Siblings: No Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples. He’s an incredible violinist and improv studio musician. Taught himself to code at the age of 13.
  • 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, Light Eyesight:
    Freckles: None Hair Texture:
    Health Status: Skin Tone: Medium Dominant Hand:
    Year of Birth: 1930 Cause of Death: Old age Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: 85 Body Hair: Straight
    Weight: 160 lbs. (72 kg) Occupation: Pastor Eye Color: Brown, Dark
    Half Siblings: Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision. Built houses for Habitat for Humanity.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture: Fine
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1930 Cause of Death: Old age complications Hair Loss:
    Height: 5'04" (162.56 cm) Age at Death: 83 Body Hair:
    Weight: 150 lbs. (68 kg) Occupation: Homemaker Eye Color: Hazel/Green
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She was an excellent bowler.
  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Brown, Medium Eyesight:
    Freckles: Hair Texture:
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1930 Cause of Death: Heart attack (poor diet, no exercise) Hair Loss: Receding
    Height: 5'08" (172.72 cm) Age at Death: 45 Body Hair:
    Weight: 180 lbs. (81 kg) Occupation: Newspaper Owner Eye Color: Green
    Half Siblings: Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision. Owned and wrote for a small independent newspaper.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Medium Eyesight:
    Freckles: None Hair Texture:
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1930 Cause of Death: Old age complications Hair Loss:
    Height: 5'05" (165.1 cm) Age at Death: 88 Body Hair: Straight
    Weight: 150 lbs. (68 kg) Occupation: Homemaker Eye Color: Hazel/Green
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision.
    FAMILY MEMBER:
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Skin Tone: Dominant Hand:
    Year of Birth: 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 #40013

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?

Call 1-706-733-0130 or click here to chat with us.

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.