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
RS886044723 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS886044733 Health Risk Conflicting classifications of pathogenicity Severe early-childhood-onset retinal dystrophy, ABCA4-related disorder, Retinal dystrophy
RS886044737 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Optic atrophy, Retinal dystrophy
RS886044743 Health Risk Conflicting classifications of pathogenicity Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS886044762 Health Risk Conflicting classifications of pathogenicity Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS886046565 Health Risk Conflicting classifications of pathogenicity ABCA4-related disorder, ABCA4-related disorder
RS891533398 Health Risk Conflicting classifications of pathogenicity
RS913030626 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinitis pigmentosa, Retinal dystrophy
RS942734318 Health Risk Conflicting classifications of pathogenicity Stargardt disease, Stargardt disease
RS966434923 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS1012284944 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1046550021 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS1064793007 Health Risk Likely pathogenic
RS1064793008 Health Risk Likely pathogenic
RS1064793012 Health Risk Likely pathogenic
RS1064793015 Health Risk Likely pathogenic
RS1131691262 Health Risk Likely pathogenic
RS1166357291 Health Risk Likely pathogenic Stargardt disease, ABCA4-related disorder, Stargardt disease
RS1212420029 Health Risk Likely pathogenic
RS1246844424 Health Risk Likely pathogenic Retinal dystrophy, Inborn genetic diseases, ABCA4-related retinopathy
RS1264338576 Health Risk Likely pathogenic
RS1297857869 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1316934987 Health Risk Likely pathogenic
RS1362964563 Health Risk Likely pathogenic Retinal dystrophy, Age related macular degeneration 2, Severe early-childhood-onset retinal dystrophy
RS138359497 Health Risk Likely pathogenic Cone-rod dystrophy 3, Age related macular degeneration 2, Severe early-childhood-onset retinal dystrophy
RS1388219872 Health Risk Likely pathogenic Stargardt disease, Stargardt disease
RS1394101107 Health Risk Likely pathogenic
RS141823837 Health Risk Likely pathogenic Retinal dystrophy, ABCA4-related disorder, Cone-rod dystrophy 3
RS1435203678 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS143797418 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Stargardt disease
RS147826775 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS148015012 Health Risk Likely pathogenic Retinal dystrophy, Age related macular degeneration 2, Severe early-childhood-onset retinal dystrophy
RS148460146 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Retinitis pigmentosa 19
RS1553186509 Health Risk Likely pathogenic Congenital stationary night blindness, Congenital stationary night blindness
RS1553188682 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1553189507 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1553192432 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS1553195472 Health Risk Likely pathogenic Macular dystrophy, Macular dystrophy
RS1557768924 Health Risk Likely pathogenic
RS1557778273 Health Risk Likely pathogenic
RS1570367144 Health Risk Likely pathogenic Stargardt disease, Stargardt disease
RS1570377836 Health Risk Likely pathogenic
RS1570377861 Health Risk Likely pathogenic Stargardt disease, Retinal dystrophy, Stargardt disease
RS1570380080 Health Risk Likely pathogenic Stargardt disease, Stargardt disease
RS1570382663 Health Risk Likely pathogenic Retinitis pigmentosa, Cone-rod dystrophy 3, Retinitis pigmentosa
RS1570387558 Health Risk Likely pathogenic
RS1570393848 Health Risk Likely pathogenic Cone-rod dystrophy 3, Cone-rod dystrophy 3
RS1570433137 Health Risk Likely pathogenic Stargardt disease, Stargardt disease
RS1571241947 Health Risk Likely pathogenic Stargardt disease, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS1571242070 Health Risk Likely pathogenic Cone-rod dystrophy, Age related macular degeneration 2, Stargardt disease
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