ABCA4 Chromosome 1

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

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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
RS2523751766 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2523752501 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS2523760441 Health Risk Pathogenic
RS2523760594 Health Risk Pathogenic
RS2523771313 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2523771540 Health Risk Pathogenic Retinitis pigmentosa 19, Retinitis pigmentosa 19
RS2523774251 Health Risk Pathogenic
RS2523774434 Health Risk Pathogenic
RS2523778270 Health Risk Pathogenic
RS2523780097 Health Risk Pathogenic
RS2523780335 Health Risk Pathogenic
RS2523790513 Health Risk Pathogenic
RS2523791093 Health Risk Pathogenic
RS2523791122 Health Risk Pathogenic
RS2523791418 Health Risk Pathogenic
RS2523797555 Health Risk Pathogenic
RS2523797636 Health Risk Pathogenic
RS2523805141 Health Risk Pathogenic
RS2523805441 Health Risk Pathogenic
RS2523822381 Health Risk Pathogenic
RS2523832548 Health Risk Pathogenic
RS2523832712 Health Risk Pathogenic
RS2523832753 Health Risk Pathogenic Retinitis pigmentosa, Severe early-childhood-onset retinal dystrophy, Age related macular degeneration 2
RS2523832903 Health Risk Pathogenic
RS2523833102 Health Risk Pathogenic Stargardt disease 3, Stargardt disease 3
RS2523841187 Health Risk Pathogenic
RS2523841751 Health Risk Pathogenic
RS2523841893 Health Risk Pathogenic
RS2523841936 Health Risk Pathogenic
RS2523843294 Health Risk Pathogenic
RS2523844007 Health Risk Pathogenic
RS2523844235 Health Risk Pathogenic
RS2523891438 Health Risk Pathogenic
RS2523894686 Health Risk Pathogenic
RS2523894863 Health Risk Pathogenic
RS2523895047 Health Risk Pathogenic
RS2523895384 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS2523895442 Health Risk Pathogenic
RS2523897592 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2523897865 Health Risk Pathogenic
RS2523902047 Health Risk Pathogenic
RS2523902363 Health Risk Pathogenic
RS2523902375 Health Risk Pathogenic
RS2523965353 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS2523965705 Health Risk Pathogenic
RS2523965817 Health Risk Pathogenic
RS2523966504 Health Risk Pathogenic
RS2523979862 Health Risk Pathogenic
RS2523980194 Health Risk Pathogenic
RS2523980415 Health Risk Pathogenic
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