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
RS2523771800 Health Risk Likely pathogenic
RS2523773776 Health Risk Likely pathogenic
RS2523780315 Health Risk Likely pathogenic
RS2523780433 Health Risk Likely pathogenic
RS2523790517 Health Risk Likely pathogenic
RS2523797746 Health Risk Likely pathogenic
RS2523816358 Health Risk Likely pathogenic Stargardt disease, Stargardt disease
RS2523817213 Health Risk Likely pathogenic
RS2523817445 Health Risk Likely pathogenic
RS2523821836 Health Risk Likely pathogenic
RS2523821851 Health Risk Likely pathogenic
RS2523833166 Health Risk Likely pathogenic
RS2523841647 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2523843902 Health Risk Likely pathogenic
RS2523843951 Health Risk Likely pathogenic
RS2523890741 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS2523965931 Health Risk Likely pathogenic Stargardt disease, Stargardt disease
RS2523979805 Health Risk Likely pathogenic
RS2523979837 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS2523980607 Health Risk Likely pathogenic Stargardt disease, Stargardt disease
RS2523999188 Health Risk Likely pathogenic Stargardt disease 3, Stargardt disease 3
RS2524047809 Health Risk Likely pathogenic
RS2524047814 Health Risk Likely pathogenic
RS2524048090 Health Risk Likely pathogenic
RS28938473 Health Risk Likely pathogenic Stargardt disease, Severe early-childhood-onset retinal dystrophy, Retinal dystrophy
RS369440533 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS376947008 Health Risk Likely pathogenic Cone-rod dystrophy 3, Cone-rod dystrophy 3
RS553776104 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS55732384 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Cone-rod dystrophy 3, Age related macular degeneration 2
RS61748526 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Retinitis pigmentosa, Severe early-childhood-onset retinal dystrophy
RS61748532 Health Risk Likely pathogenic Retinal dystrophy, Severe early-childhood-onset retinal dystrophy, Stargardt disease
RS61748534 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Cone-rod dystrophy 3, Severe early-childhood-onset retinal dystrophy
RS61748545 Health Risk Likely pathogenic Macular dystrophy, Retinal dystrophy, Cone-rod dystrophy 3
RS61749416 Health Risk Likely pathogenic
RS61749428 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS61749432 Health Risk Likely pathogenic
RS61749436 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS61749449 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS61749451 Health Risk Likely pathogenic Retinal dystrophy, Retinitis pigmentosa, Cone-rod dystrophy 3
RS61749453 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS61750128 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS61750139 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS61750148 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS61750158 Health Risk Likely pathogenic Cone-rod dystrophy 3, Cone-rod dystrophy 3
RS61750564 Health Risk Likely pathogenic Severe early-childhood-onset retinal dystrophy, Retinitis pigmentosa 19, Cone-rod dystrophy 3
RS61750568 Health Risk Likely pathogenic
RS61750636 Health Risk Likely pathogenic Retinitis pigmentosa, Retinitis pigmentosa
RS61750639 Health Risk Likely pathogenic Retinitis pigmentosa, Retinal dystrophy, Severe early-childhood-onset retinal dystrophy
RS61750642 Health Risk Likely pathogenic Stargardt disease, Stargardt disease
RS61750655 Health Risk Likely pathogenic Stargardt disease, Stargardt disease
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