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
RS1366296798 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1373168392 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1376036671 Health Risk Pathogenic
RS137853898 Health Risk Pathogenic
RS1385119665 Health Risk Pathogenic Retinal dystrophy, ABCA4-related disorder, Severe early-childhood-onset retinal dystrophy
RS1388510409 Health Risk Pathogenic
RS1396816886 Health Risk Pathogenic
RS1401924846 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS140671840 Health Risk Pathogenic
RS1410550128 Health Risk Pathogenic
RS1417184535 Health Risk Pathogenic Retinal dystrophy, ABCA4-related retinopathy, Retinal dystrophy
RS1428504985 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1437993640 Health Risk Pathogenic Stargardt disease, Retinal dystrophy, Stargardt disease
RS1439783011 Health Risk Pathogenic
RS1440824352 Health Risk Pathogenic
RS1448468321 Health Risk Pathogenic Retinal dystrophy, Inborn genetic diseases, Retinal dystrophy
RS1453899480 Health Risk Pathogenic
RS1457937638 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1467000353 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1475966997 Health Risk Pathogenic
RS148234178 Health Risk Pathogenic ABCA4-related retinopathy, Retinitis pigmentosa, ABCA4-related retinopathy
RS149381884 Health Risk Pathogenic
RS150686179 Health Risk Pathogenic
RS150774447 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Stargardt disease, ABCA4-related disorder
RS1553187160 Health Risk Pathogenic Cone-rod dystrophy 3, Cone-rod dystrophy 3
RS1553187162 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1553187228 Health Risk Pathogenic
RS1553190559 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1553190664 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1553192726 Health Risk Pathogenic Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa
RS1553193813 Health Risk Pathogenic Retinal dystrophy, Cone-rod dystrophy 3, Retinal dystrophy
RS1553196583 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1557768952 Health Risk Pathogenic
RS1557770132 Health Risk Pathogenic
RS1557787559 Health Risk Pathogenic Cone-rod dystrophy 3, Cone-rod dystrophy 3
RS1557787756 Health Risk Pathogenic maculopathy, Severe early-childhood-onset retinal dystrophy, Retinitis pigmentosa 19
RS1557795571 Health Risk Pathogenic
RS1570367230 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1570370826 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1570370929 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1570373408 Health Risk Pathogenic Cone-rod dystrophy 3, Retinal dystrophy, Cone-rod dystrophy 3
RS1570386206 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1570392557 Health Risk Pathogenic
RS1570393727 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1570407032 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1570426448 Health Risk Pathogenic
RS1571239957 Health Risk Pathogenic
RS1571243037 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1571245809 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1571250020 Health Risk Pathogenic Cone-rod dystrophy, Cone-rod dystrophy
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