Meet Gage (12011) – Open ID Donor.

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Gage has a lean build, with a slender torso and shoulders and toned, muscular legs. He has medium skin which tans very well in the summer, brown hair, bright blue/green eyes, and a dazzling smile. He has a handsome, angular face, great cheekbones, and a prominent nose.

Gage is an avid naturalist and wilderness explorer. He studied Marine Biology, has lead whaling tours off the coast of the PNW, as well as his current job as a naturalist and hiking guide for a private wilderness exploration cruise tour in Alaska. He also loves kayaking, skiing, and ultimate Frisbee, making him the perfect PNW outdoorsmen archetype. Gage loves to engage in conversation with everyone in the office; he is thoughtful, genuine, and kind, as well as a fantastic story teller, which puts him among the top favorites of the staff. If you are looking for someone who is outgoing, courageous, and full of spirit, Gage would be a great choice for you!

 

 

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