Meet Zane (9924) – Open ID Donor.

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Zane has a very muscular build, a result of a regular cardiovascular and heavy weightlifting exercise regime. He has dark green eyes that stand out against his olive skin tone and wavy brown hair. Zane is clean-cut, with short cut hair and a smooth complexion that is always clean shaven. He has a pink lips that form a wide smile with straight white teeth. Zane has strong features set in a slightly round face giving him a sweet and attractive quality.

Zane embodies the Midwest persona. He is sweet, polite, outgoing and always ready to lend a helping hand. Zane is very genuine and outgoing and makes friends wherever he goes. He is also athletic and musical, playing a variety of instruments. When asked why he wants to be a donor, Zane answered, “A child is the passing on of the legacy of life and contributing to that is the least I can do.” We cannot brag about Zane enough, he is a truly wonderful person and we love having him in the program.

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