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
RS2101042802 Health Risk Pathogenic
RS2101042844 Health Risk Pathogenic
RS2101043601 Health Risk Pathogenic
RS2101047010 Health Risk Pathogenic
RS2101047091 Health Risk Pathogenic
RS2101048479 Health Risk Pathogenic Retinitis pigmentosa 19, Retinitis pigmentosa 19
RS2101050504 Health Risk Pathogenic
RS2101050573 Health Risk Pathogenic
RS2101050587 Health Risk Pathogenic
RS2101050605 Health Risk Pathogenic Stargardt disease, Retinal dystrophy, Stargardt disease
RS2101051331 Health Risk Pathogenic
RS2101051468 Health Risk Pathogenic
RS2101053424 Health Risk Pathogenic
RS2101053527 Health Risk Pathogenic
RS2101053584 Health Risk Pathogenic
RS2101053587 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2101057076 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS2101057149 Health Risk Pathogenic ABCA4-related retinopathy, ABCA4-related retinopathy
RS2101057370 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS2101059717 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS2101067575 Health Risk Pathogenic Retinitis pigmentosa 19, Retinitis pigmentosa 19
RS2101067647 Health Risk Pathogenic
RS2101069632 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2101069758 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2101069863 Health Risk Pathogenic
RS2101075191 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2101076246 Health Risk Pathogenic
RS2101078030 Health Risk Pathogenic
RS2101078370 Health Risk Pathogenic
RS2101078386 Health Risk Pathogenic
RS2101078482 Health Risk Pathogenic Stargardt disease 3, Stargardt disease 3
RS2101079010 Health Risk Pathogenic
RS2101079015 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2101079061 Health Risk Pathogenic
RS2101079369 Health Risk Pathogenic
RS2101079417 Health Risk Pathogenic
RS2101101226 Health Risk Pathogenic
RS2101101348 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2101101390 Health Risk Pathogenic
RS2101101428 Health Risk Pathogenic
RS2101104619 Health Risk Pathogenic
RS2101106481 Health Risk Pathogenic
RS2101106559 Health Risk Pathogenic
RS2101106686 Health Risk Pathogenic
RS2101106736 Health Risk Pathogenic
RS2101107081 Health Risk Pathogenic
RS2101135446 Health Risk Pathogenic
RS2101155690 Health Risk Pathogenic
RS2101156021 Health Risk Pathogenic
RS2101156053 Health Risk Pathogenic
« Prev 1 ... 14 15 16 17 18 19 20 ... 28 Next »
Sign Up to Analyze Your DNA Log In