RecName: Full=Solute carrier family 38 member 8; AltName: Full=Amino a - Protein

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The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences. [Invest Ophthalmol Vis Sci. 2022]
The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences.
Kruijt CC, Gradstein L, Bergen AA, Florijn RJ, Arveiler B, Lasseaux E, Zanlonghi X, Bagdonaite-Bejarano L, Fulton AB, Yahalom C, et al. Invest Ophthalmol Vis Sci. 2022 Jan 3; 63(1):19.
Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia. [Int J Mol Sci. 2021]
Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia.
Schiff ER, Tailor VK, Chan HW, Theodorou M, Webster AR, Moosajee M. Int J Mol Sci. 2021 Jan 24; 22(3). Epub 2021 Jan 24.
The pathogenicity of SLC38A8 in five families with foveal hypoplasia and congenital nystagmus. [Exp Eye Res. 2020]
The pathogenicity of SLC38A8 in five families with foveal hypoplasia and congenital nystagmus.
Weiner C, Hecht I, Rotenstreich Y, Guttman S, Or L, Morad Y, Shapira G, Shomron N, Pras E. Exp Eye Res. 2020 Apr; 193:107958. Epub 2020 Feb 4.

RefSeq genomic sequence
See the genomic reference sequence for the SLC38A8 gene (NG_034136.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the SLC38A8 gene.

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A6NNN8 [Domain Mapping of Disease Mut...]
A6NNN8
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein