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TYR

tyrosinase

gene with protein productOMIM: 6069335 заболеваний
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in4
Minimal pigment oculocutaneous albinism type 1ORPHA:352734
→
Temperature-sensitive oculocutaneous albinism type 1ORPHA:352737
→
Oculocutaneous albinism type 1BORPHA:79434
→
Oculocutaneous albinism type 1AORPHA:79431
→
Модифицирующая мутация1
Waardenburg syndrome type 2ORPHA:895
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Данные: Orphadata (CC-BY-4.0)