SLC38A8 Chromosome 16

Solute carrier family 38 member 8
64 variants 64 Health Risk

Upload your DNA to see your personal genotypes for variants in SLC38A8.

What This Gene Does
This gene encodes a putative sodium-dependent amino-acid/proton antiporter. The protein has eleven transmembrane domains, an extracellular N-terminus and an intracellular C-terminal tail. The protein is a member of the SLC38 sodium-coupled neutral amino acid transporter family of proteins. Mutations in this gene result in foveal hypoplasia with or without optic nerve misrouting and/or anterior segment dysgenesis. [provided by RefSeq, May 2014]
Gene Info
Gene Group
Solute carrier family 38
Locus Type
gene with protein product
Location
16q23.3
Ensembl
ENSG00000166558
Associated Conditions (9)
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
Inborn genetic diseases
SLC38A8-related disorder
Uterine corpus endometrial carcinoma
Leber congenital amaurosis
Foveal hypoplasia
FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING AND ANTERIOR SEGMENT DYSGENESIS
FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING
Foveal hypoplasia 2 and optic nerve misrouting with or without anterior segment dysgenesis
Key Variants
RS139373929
Conflicting classifications of pathogenicity
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Inborn genetic diseases, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
Health Risk
RS150844985
Conflicting classifications of pathogenicity
Inborn genetic diseases, SLC38A8-related disorder, Uterine corpus endometrial carcinoma
Health Risk
RS376444481
Conflicting classifications of pathogenicity
Health Risk
RS760391436
Conflicting classifications of pathogenicity
Leber congenital amaurosis, Leber congenital amaurosis
Health Risk
RS778342318
Conflicting classifications of pathogenicity
Health Risk
RS1057516193
Likely pathogenic
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
Health Risk
RS1057521634
Likely pathogenic
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
Health Risk
RS1178023478
Likely pathogenic
Health Risk
RS1264151343
Likely pathogenic
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
Health Risk
RS1264247948
Likely pathogenic
Health Risk
RS1306823741
Likely pathogenic
Health Risk
RS1325791118
Likely pathogenic
Health Risk
All Variants (64)
RSID Category Clinical Significance Conditions
RS139373929 Health Risk Conflicting classifications of pathogenicity Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Inborn genetic diseases, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS150844985 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, SLC38A8-related disorder, Uterine corpus endometrial carcinoma
RS376444481 Health Risk Conflicting classifications of pathogenicity
RS760391436 Health Risk Conflicting classifications of pathogenicity Leber congenital amaurosis, Leber congenital amaurosis
RS778342318 Health Risk Conflicting classifications of pathogenicity
RS1057516193 Health Risk Likely pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS1057521634 Health Risk Likely pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS1178023478 Health Risk Likely pathogenic
RS1264151343 Health Risk Likely pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS1264247948 Health Risk Likely pathogenic
RS1306823741 Health Risk Likely pathogenic
RS1325791118 Health Risk Likely pathogenic
RS1379690075 Health Risk Likely pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS1409386171 Health Risk Likely pathogenic
RS1463272578 Health Risk Likely pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS149436446 Health Risk Likely pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS2085112203 Health Risk Likely pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS2507616467 Health Risk Likely pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS2507631270 Health Risk Likely pathogenic
RS2507631710 Health Risk Likely pathogenic
RS2507659020 Health Risk Likely pathogenic
RS374872713 Health Risk Likely pathogenic
RS376096200 Health Risk Likely pathogenic
RS779197965 Health Risk Likely pathogenic
RS903298698 Health Risk Likely pathogenic
RS1251780383 Health Risk Pathogenic
RS1256250716 Health Risk Pathogenic
RS1310357008 Health Risk Pathogenic
RS1335352747 Health Risk Pathogenic
RS146899328 Health Risk Pathogenic
RS1473492838 Health Risk Pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS1597273765 Health Risk Pathogenic Foveal hypoplasia, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia
RS2085111611 Health Risk Pathogenic
RS2085211910 Health Risk Pathogenic
RS2151131708 Health Risk Pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS2507618267 Health Risk Pathogenic
RS2507631298 Health Risk Pathogenic
RS2507654719 Health Risk Pathogenic
RS2507659253 Health Risk Pathogenic
RS2507659781 Health Risk Pathogenic
RS2507659939 Health Risk Pathogenic
RS2507668196 Health Risk Pathogenic
RS2507668346 Health Risk Pathogenic
RS2507668848 Health Risk Pathogenic
RS2507668893 Health Risk Pathogenic
RS2507681732 Health Risk Pathogenic
RS587777253 Health Risk Pathogenic Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome, Foveal hypoplasia, Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome
RS587777254 Health Risk Pathogenic FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING AND ANTERIOR SEGMENT DYSGENESIS, FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING AND ANTERIOR SEGMENT DYSGENESIS
RS587777255 Health Risk Pathogenic FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING AND ANTERIOR SEGMENT DYSGENESIS, Inborn genetic diseases, FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING AND ANTERIOR SEGMENT DYSGENESIS
RS587777256 Health Risk Pathogenic FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING, FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE MISROUTING
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