OCA2 Chromosome 15

OCA2 melanosomal transmembrane protein
330 variants 330 Health Risk

Upload your DNA to see your personal genotypes for variants in OCA2.

What This Gene Does
This gene encodes the human homolog of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis. It is involved in mammalian pigmentation, where it may control skin color variation and act as a determinant of brown or blue eye color. Mutations in this gene result in type 2 oculocutaneous albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]
Gene Info
Gene Group
Solute carrier family 13
Locus Type
gene with protein product
Location
15q12-q13.1
Ensembl
ENSG00000104044
Associated Conditions (18)
Tyrosinase-positive oculocutaneous albinism
OCA2-related disorder
SKIN/HAIR/EYE PIGMENTATION 1
BLUE/NONBLUE EYES
Oculocutaneous albinism
Albinism
Nonsyndromic Oculocutaneous Albinism
Albinism or congenital nystagmus
Uveal melanoma
Ovarian serous cystadenocarcinoma
Inborn genetic diseases
Cone-rod dystrophy
6 conditions
Clear cell carcinoma of kidney
Brown oculocutaneous albinism
Hypophosphatasia
See cases
Melanoma
Key Variants
RS1046172334
Conflicting classifications of pathogenicity
Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
Health Risk
RS1158730024
Conflicting classifications of pathogenicity
Health Risk
RS1258451850
Conflicting classifications of pathogenicity
OCA2-related disorder, OCA2-related disorder
Health Risk
RS1277911369
Conflicting classifications of pathogenicity
SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES, Tyrosinase-positive oculocutaneous albinism
Health Risk
RS1325388159
Conflicting classifications of pathogenicity
Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
Health Risk
RS1374558186
Conflicting classifications of pathogenicity
SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES, OCA2-related disorder
Health Risk
RS137956605
Conflicting classifications of pathogenicity
Tyrosinase-positive oculocutaneous albinism, OCA2-related disorder, Tyrosinase-positive oculocutaneous albinism
Health Risk
RS138065338
Conflicting classifications of pathogenicity
Tyrosinase-positive oculocutaneous albinism, SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES
Health Risk
RS1391198560
Conflicting classifications of pathogenicity
Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
Health Risk
RS140566426
Conflicting classifications of pathogenicity
Tyrosinase-positive oculocutaneous albinism, SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES
Health Risk
RS140932222
Conflicting classifications of pathogenicity
Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
Health Risk
RS141603023
Conflicting classifications of pathogenicity
Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
Health Risk
All Variants (330)
RSID Category Clinical Significance Conditions
RS2035478131 Health Risk Pathogenic
RS2036555943 Health Risk Pathogenic Tyrosinase-positive oculocutaneous albinism, OCA2-related disorder, Tyrosinase-positive oculocutaneous albinism
RS2036558249 Health Risk Pathogenic Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
RS2040042896 Health Risk Pathogenic
RS2041230041 Health Risk Pathogenic
RS2041526018 Health Risk Pathogenic
RS2042342323 Health Risk Pathogenic
RS2042387354 Health Risk Pathogenic
RS2042625844 Health Risk Pathogenic
RS2140668412 Health Risk Pathogenic
RS2140824287 Health Risk Pathogenic
RS2140965742 Health Risk Pathogenic Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
RS2140978976 Health Risk Pathogenic
RS2141229433 Health Risk Pathogenic
RS2504084532 Health Risk Pathogenic
RS2505163641 Health Risk Pathogenic
RS2506065436 Health Risk Pathogenic OCA2-related disorder, OCA2-related disorder
RS2506065459 Health Risk Pathogenic
RS2506065990 Health Risk Pathogenic
RS2506396018 Health Risk Pathogenic
RS2506396936 Health Risk Pathogenic
RS2506400688 Health Risk Pathogenic
RS2506495202 Health Risk Pathogenic
RS2506495474 Health Risk Pathogenic
RS2506575006 Health Risk Pathogenic
RS2506825899 Health Risk Pathogenic
RS2524458707 Health Risk Pathogenic Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
RS2548282084 Health Risk Pathogenic
RS2548338599 Health Risk Pathogenic
RS2548339234 Health Risk Pathogenic SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES, Tyrosinase-positive oculocutaneous albinism
RS2548339389 Health Risk Pathogenic
RS2548345341 Health Risk Pathogenic
RS2548345604 Health Risk Pathogenic
RS2548345877 Health Risk Pathogenic Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
RS2548350055 Health Risk Pathogenic
RS2548363425 Health Risk Pathogenic
RS2548363498 Health Risk Pathogenic Oculocutaneous albinism, Oculocutaneous albinism
RS2548363750 Health Risk Pathogenic
RS2548435013 Health Risk Pathogenic
RS2548435190 Health Risk Pathogenic
RS2548435739 Health Risk Pathogenic
RS2548453019 Health Risk Pathogenic
RS2548453877 Health Risk Pathogenic
RS2548474354 Health Risk Pathogenic
RS2548495118 Health Risk Pathogenic
RS2548495468 Health Risk Pathogenic
RS2548495570 Health Risk Pathogenic Tyrosinase-positive oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism
RS2548670988 Health Risk Pathogenic
RS2548671431 Health Risk Pathogenic SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES, SKIN/HAIR/EYE PIGMENTATION 1
RS2548672995 Health Risk Pathogenic
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