Meet Kirk (12039) – Open ID Donor.

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  • Eyes: Green
  • Hair: Strawberry Blonde
  • Height: 6'04"
  • Weight (lbs): 235
  • Blood: O Rh+
  • CMV: -
  • Ethnicity: Caucasian, Czech, English, Irish, Italian, Polish, Scottish
  • Jewish Ancestry: No
  • Education/Occupation: Masters Computer Science / Data Scientist
  • Live Birth / Pregnancy Confirmed: Yes
  • Extended Testing: Yes
  • Genetically tested for: View

Kirk’s thick wavy strawberry blonde hair is kept long. He has a full beard that he keeps nicely groomed and professional. His fair complexion and light dusting of freckles across his nose complete his charming look. Kirk has a sturdy build with broad shoulders and defined chest. He has long arms and legs that suit his tall 6’4” frame.

Kirk is extremely smart with a background in computer science and strong mathematical skills. He is very handy around the house and can pretty much fix anything that is put in front of him. Kirk can come off a bit shy at first but opens up in the right situations. Kirk is a family man with a big heart and kind demeanor. He would make a great choice for any family!

Genetic Testing

Over the years, we have expanded our 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. All donors have undergone genetic testing for Cystic Fibrosis, Spinal Muscular Atrophy and Karyotyping.  However, many donors have had more extensive testing performed.

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.

Karyotyping  Normal Male Karyoptype, 46XY
ABCC8-related hyperinsulinism Non-Carrier
alpha thalassemia Non-Carrier
ARSACS Non-Carrier
Bloom syndrome Non-Carrier
Canavan disease Non-Carrier
cystic fibrosis Non-Carrier
familial dysautonomia Non-Carrier
Fanconi anemia type C Non-Carrier
Gaucher disease Non-Carrier
glycogen storage disease type Ia Non-Carrier
Hb beta chain-related hemoglobinopathy (including beta thalassemia and sickle cell disease) No disease-causing mutations detected; normal complete blood count and hemoglobin analysis
hexosaminidase A deficiency (including Tay-Sachs disease) Non-Carrier
Joubert syndrome 2 Non-Carrier
lipoamide dehydrogenase deficiency Non-Carrier
maple syrup urine disease type 1B Non-Carrier
mucolipidosis IV Non-Carrier
NEB-related nemaline myopathy Non-Carrier
Niemann-Pick disease, SMPD1-associated Non-Carrier
spinal muscular atrophy No disease-causing mutations detected (2 copies or more)
Usher syndrome type 1F Non-Carrier
Usher syndrome type 3 Non-Carrier
Walker-Warburg syndrome Non-Carrier