solute carrier family 7 member 7 isoform 1, partial [Homo sapiens]

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[Clinical features of children with lysinuric protein intolerance and SLC7A7 gene mutation: an analysis of 3 cases]. [Zhongguo Dang Dai Er Ke Za Zhi...]
[Clinical features of children with lysinuric protein intolerance and SLC7A7 gene mutation: an analysis of 3 cases].
Cui D, Hu YH, Tang G, Shen D, Chen L, Liao JX, Chen SL. Zhongguo Dang Dai Er Ke Za Zhi. 2019 Apr; 21(4):375-380.
Analysis of LPI-causing mutations on y+LAT1 function and localization. [Orphanet J Rare Dis. 2019]
Analysis of LPI-causing mutations on y+LAT1 function and localization.
Rotoli BM, Barilli A, Ingoglia F, Visigalli R, Bianchi MG, Ferrari F, Martinelli D, Dionisi-Vici C, Dall'Asta V. Orphanet J Rare Dis. 2019 Mar 4; 14(1):63. Epub 2019 Mar 4.
Function of SLC7A7 in T-Cell Acute Lymphoblastic Leukemia. [Cell Physiol Biochem. 2018]
Function of SLC7A7 in T-Cell Acute Lymphoblastic Leukemia.
Ji X, Yang X, Wang N, Kang M, Wang Y, Rong L, Fang Y, Xue Y. Cell Physiol Biochem. 2018; 48(2):731-740. Epub 2018 Jul 19.

RefSeq genomic sequence
See the genomic reference sequence for the SLC7A7 gene (NG_012851.2).
RefSeq protein isoforms
See 7 reference sequence protein isoforms for the SLC7A7 gene.

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Protein