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
RS1662601425 Health Risk Pathogenic Stargardt disease 3, Retinitis pigmentosa 19, Stargardt disease 3
RS1662935816 Health Risk Pathogenic Generalized choriocapillaris dystrophy, Generalized choriocapillaris dystrophy
RS1800553 Health Risk Pathogenic MACULAR DEGENERATION, AGE-RELATED, 2
RS1800728 Health Risk Pathogenic Cone-rod dystrophy 3, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS192656357 Health Risk Pathogenic
RS200967229 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Stargardt disease
RS201471607 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Stargardt disease, Retinitis pigmentosa
RS201738997 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Abnormality of the eye, Retinal dystrophy
RS201855602 Health Risk Pathogenic Stargardt disease, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS202198282 Health Risk Pathogenic
RS2100987980 Health Risk Pathogenic
RS2100988221 Health Risk Pathogenic ABCA4-related retinopathy, ABCA4-related retinopathy
RS2100988422 Health Risk Pathogenic
RS2100993531 Health Risk Pathogenic
RS2100993760 Health Risk Pathogenic
RS2100994047 Health Risk Pathogenic
RS2100995699 Health Risk Pathogenic
RS2101000353 Health Risk Pathogenic
RS2101000357 Health Risk Pathogenic
RS2101000542 Health Risk Pathogenic
RS2101004096 Health Risk Pathogenic
RS2101007411 Health Risk Pathogenic
RS2101007419 Health Risk Pathogenic
RS2101007643 Health Risk Pathogenic
RS2101008577 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2101013784 Health Risk Pathogenic
RS2101015376 Health Risk Pathogenic
RS2101015583 Health Risk Pathogenic
RS2101020591 Health Risk Pathogenic
RS2101020760 Health Risk Pathogenic
RS2101022823 Health Risk Pathogenic Cone-rod dystrophy 3, Retinal dystrophy, Cone-rod dystrophy 3
RS2101022885 Health Risk Pathogenic
RS2101022969 Health Risk Pathogenic
RS2101023129 Health Risk Pathogenic Retinal dystrophy, Severe early-childhood-onset retinal dystrophy, Retinal dystrophy
RS2101023641 Health Risk Pathogenic
RS2101024039 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2101025946 Health Risk Pathogenic
RS2101027758 Health Risk Pathogenic Age related macular degeneration 2, Age related macular degeneration 2
RS2101027818 Health Risk Pathogenic
RS2101033438 Health Risk Pathogenic
RS2101033562 Health Risk Pathogenic
RS2101033677 Health Risk Pathogenic
RS2101033821 Health Risk Pathogenic
RS2101034641 Health Risk Pathogenic
RS2101035684 Health Risk Pathogenic
RS2101035787 Health Risk Pathogenic
RS2101036750 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinitis pigmentosa, Severe early-childhood-onset retinal dystrophy
RS2101036893 Health Risk Pathogenic
RS2101037158 Health Risk Pathogenic
RS2101037211 Health Risk Pathogenic
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