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
RS1660350150 Health Risk Pathogenic Retinitis pigmentosa 19, Stargardt disease, Retinitis pigmentosa 19
RS1660360960 Health Risk Pathogenic
RS1660366419 Health Risk Pathogenic
RS1660368021 Health Risk Pathogenic
RS1660447204 Health Risk Pathogenic Cone dystrophy, Cone dystrophy
RS1660480045 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1660527423 Health Risk Pathogenic ABCA4-related retinopathy, ABCA4-related retinopathy
RS1660531880 Health Risk Pathogenic
RS1660573507 Health Risk Pathogenic
RS1660619132 Health Risk Pathogenic
RS1660619835 Health Risk Pathogenic
RS1660626613 Health Risk Pathogenic Age related macular degeneration 2, Age related macular degeneration 2
RS1660700107 Health Risk Pathogenic
RS1660700260 Health Risk Pathogenic Stargardt disease 3, Stargardt disease 3
RS1660702616 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1660761326 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1660762877 Health Risk Pathogenic Generalized choriocapillaris dystrophy, Generalized choriocapillaris dystrophy
RS1660844241 Health Risk Pathogenic
RS1660844326 Health Risk Pathogenic Isolated macular dystrophy, Isolated macular dystrophy
RS1660845802 Health Risk Pathogenic Cone dystrophy, Cone dystrophy
RS1660936779 Health Risk Pathogenic Isolated macular dystrophy, Isolated macular dystrophy
RS1660937747 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1660944269 Health Risk Pathogenic Severe early-childhood-onset retinal dystrophy, Cone-rod dystrophy 3, Age related macular degeneration 2
RS1660945616 Health Risk Pathogenic
RS1660983058 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1660993544 Health Risk Pathogenic
RS1660996754 Health Risk Pathogenic
RS1661097693 Health Risk Pathogenic
RS1661098509 Health Risk Pathogenic Retinitis pigmentosa, Severe early-childhood-onset retinal dystrophy, Retinitis pigmentosa
RS1661163134 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1661165160 Health Risk Pathogenic
RS1661166046 Health Risk Pathogenic
RS1661181033 Health Risk Pathogenic
RS1661577361 Health Risk Pathogenic Stargardt disease, Retinal dystrophy, Stargardt disease
RS1661578005 Health Risk Pathogenic Stargardt disease 3, Stargardt disease 3
RS1661578607 Health Risk Pathogenic
RS1661623028 Health Risk Pathogenic
RS1661660701 Health Risk Pathogenic
RS1661666701 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1661669685 Health Risk Pathogenic Retinal dystrophy, Retinal dystrophy
RS1661692833 Health Risk Pathogenic
RS1661749935 Health Risk Pathogenic
RS1662191792 Health Risk Pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS1662213462 Health Risk Pathogenic Cone-rod dystrophy, Cone-rod dystrophy
RS1662214905 Health Risk Pathogenic
RS1662216783 Health Risk Pathogenic Stargardt disease, Retinal dystrophy, Stargardt disease
RS1662327418 Health Risk Pathogenic Stargardt disease, Stargardt disease
RS1662506957 Health Risk Pathogenic
RS1662507319 Health Risk Pathogenic Cone-rod dystrophy, Cone-rod dystrophy
RS1662508844 Health Risk Pathogenic
« Prev 1 ... 12 13 14 15 16 17 18 ... 28 Next »
Sign Up to Analyze Your DNA Log In