solute carrier family 7 member 14 [Mus musculus]

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SLC7A14 imports GABA to lysosomes and impairs hepatic insulin sensitivity via inhibiting mTORC2. [Cell Rep. 2023]
SLC7A14 imports GABA to lysosomes and impairs hepatic insulin sensitivity via inhibiting mTORC2.
Jiang X, Liu K, Jiang H, Yin H, Wang ED, Cheng H, Yuan F, Xiao F, Wang F, Lu W, et al. Cell Rep. 2023 Jan 31; 42(1):111984. Epub 2023 Jan 10.
SLC7A14 linked to autosomal recessive retinitis pigmentosa. [Nat Commun. 2014]
SLC7A14 linked to autosomal recessive retinitis pigmentosa.
Jin ZB, Huang XF, Lv JN, Xiang L, Li DQ, Chen J, Huang C, Wu J, Lu F, Qu J. Nat Commun. 2014 Mar 27; 5:3517. Epub 2014 Mar 27.
Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction. [Sci Adv. 2022]
Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction.
Giffen KP, Li Y, Liu H, Zhao XC, Zhang CJ, Shen RJ, Wang T, Janesick A, Chen BB, Gong SS, et al. Sci Adv. 2022 Apr 8; 8(14):eabk0942. Epub 2022 Apr 8.

RefSeq mRNA
See reference mRNA sequence for the Slc7a14 gene (NM_172861.3).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the Slc7a14 gene.

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Ensembl
Ensembl [Ensembl]
Ensembl
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein