ABCA4 Chromosome 1

ATP binding cassette subfamily A member 4
1388 variants 1388 Health Risk

Upload your DNA to see your personal genotypes for variants in ABCA4.

What This Gene Does
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This protein is a retina-specific ABC transporter with N-retinylidene-PE as a substrate. It is expressed exclusively in retina photoreceptor cells, and the gene product mediates transport of an essental molecule, all-trans-retinal aldehyde (atRAL), across the photoreceptor cell membrane. Mutations in this gene are found in patients diagnosed with Stargardt disease, a form of juvenile-onset macular degeneration. Mutations in this gene are also associated with retinitis pigmentosa-19, cone-rod dystrophy type 3, early-onset severe retinal dystrophy, fundus flavimaculatus, and macular degeneration age-related 2. [provided by RefSeq, Sep 2019]
Gene Info
Gene Group
"ATP binding cassette subfamily A|ATPase phospholipid transporting"
Locus Type
gene with protein product
Location
1p22.1
Ensembl
ENSG00000198691
Associated Conditions (55)
Stargardt disease
Retinal dystrophy
Severe early-childhood-onset retinal dystrophy
Retinitis pigmentosa 19
ABCA4-related disorder
Cone-rod dystrophy 3
Retinitis pigmentosa
Cone dystrophy
Optic atrophy
ABCA4-related retinopathy
maculopathy
Age related macular degeneration 2
Cone-rod dystrophy
Inborn genetic diseases
Thymoma
Isolated macular dystrophy
Retinal disorder
MACULAR DEGENERATION
AGE-RELATED
2
+35 more conditions
Key Variants
All Variants (1388)
RSID Category Clinical Significance Conditions
RS2523999461 Health Risk Pathogenic
RS2523999467 Health Risk Pathogenic
RS2523999579 Health Risk Pathogenic
RS2524007787 Health Risk Pathogenic
RS2524008053 Health Risk Pathogenic
RS2524008077 Health Risk Pathogenic
RS2524008173 Health Risk Pathogenic
RS2524008286 Health Risk Pathogenic
RS2524014792 Health Risk Pathogenic Stargardt disease 3, Stargardt disease 3
RS2524048067 Health Risk Pathogenic
RS281865377 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Macular dystrophy, Retinitis pigmentosa
RS281865381 Health Risk Pathogenic
RS281865383 Health Risk Pathogenic
RS281865399 Health Risk Pathogenic
RS281865514 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS367839100 Health Risk Pathogenic Cone-rod dystrophy 3, Severe early-childhood-onset retinal dystrophy, Retinitis pigmentosa 19
RS369860406 Health Risk Pathogenic
RS369922919 Health Risk Pathogenic
RS369973540 Health Risk Pathogenic Cone-rod dystrophy 3, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS371489809 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Age related macular degeneration 2, Retinitis pigmentosa 19
RS373086027 Health Risk Pathogenic ABCA4-related retinopathy, ABCA4-related retinopathy
RS387906385 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Bietti crystalline corneoretinal dystrophy, Retinal dystrophy
RS387906387 Health Risk Pathogenic Retinal dystrophy, early-onset severe, Retinal dystrophy
RS387906388 Health Risk Pathogenic Cone-rod dystrophy 3, Cone-rod dystrophy 3
RS527236129 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS531109296 Health Risk Pathogenic ABCA4-related retinopathy, ABCA4-related retinopathy
RS542919944 Health Risk Pathogenic Stargardt disease, Retinal dystrophy, Stargardt disease
RS568627877 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Stargardt disease, Severe early-childhood-onset retinal dystrophy
RS61748517 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy, Cone dystrophy
RS61748531 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS61748533 Health Risk Pathogenic
RS61748539 Health Risk Pathogenic
RS61748542 Health Risk Pathogenic
RS61748550 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Retinitis pigmentosa 19
RS61748554 Health Risk Pathogenic Stargardt disease, Severe early-childhood-onset retinal dystrophy, Stargardt disease
RS61748555 Health Risk Pathogenic
RS61748559 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Age related macular degeneration 2
RS61749409 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Retinitis pigmentosa 19
RS61749412 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Stargardt disease, Retinal dystrophy
RS61749415 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS61749418 Health Risk Pathogenic Retinal dystrophy, Retinitis pigmentosa, Cone-rod dystrophy 3
RS61749420 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Cone-rod dystrophy 3, Age related macular degeneration 2
RS61749425 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS61749429 Health Risk Pathogenic Stargardt disease, ABCA4-related disorder, Isolated macular dystrophy
RS61749433 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Retinitis pigmentosa
RS61749438 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS61749439 Health Risk Pathogenic Age related macular degeneration 2, Age related macular degeneration 2
RS61749441 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS61749448 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS61749455 Health Risk Pathogenic Macular dystrophy, Retinal dystrophy, Age related macular degeneration 2
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