RecName: Full=Solute carrier family 7 member 14; AltName: Full=Gamma-a - Protein

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Phenotypic variability of SLC7A14 mutations in patients with inherited retinal dystrophy. [Ophthalmic Genet. 2019]
Phenotypic variability of SLC7A14 mutations in patients with inherited retinal dystrophy.
Guo LY, Zheng SL, Li J, Zhu Q, Duan WH, Zhang Y, Zhu YT, Hu M. Ophthalmic Genet. 2019 Apr; 40(2):118-123. Epub 2019 Mar 29.
Screening for SLC7A14 gene mutations in patients with autosomal recessive or sporadic retinitis pigmentosa. [Ophthalmic Genet. 2017]
Screening for SLC7A14 gene mutations in patients with autosomal recessive or sporadic retinitis pigmentosa.
Sugahara M, Oishi M, Oishi A, Ogino K, Morooka S, Gotoh N, Kang I, Yoshimura N. Ophthalmic Genet. 2017 Jan-Feb; 38(1):70-73. Epub 2016 Mar 30.
Structure and function of cationic amino acid transporters (CATs). [J Membr Biol. 2006]
Structure and function of cationic amino acid transporters (CATs).
Closs EI, Boissel JP, Habermeier A, Rotmann A. J Membr Biol. 2006; 213(2):67-77. Epub 2007 Apr 6.

RefSeq genomic sequence
See the genomic reference sequence for the SLC7A14 gene (NG_034121.1).
RefSeq protein
See the reference protein sequence for solute carrier family 7 member 14 (NP_066000.2).

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Q8TBB6 [Domain Mapping of Disease Mut...]
Q8TBB6
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Solute carrier family 7 member 14; AltName: Full=Gamma-aminobutyri...
RecName: Full=Solute carrier family 7 member 14; AltName: Full=Gamma-aminobutyric acid transporter SLC7A14
gi|296452968|sp|Q8TBB6.3|S7A14_HUMA

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