PREDICTED: Homo sapiens solute carrier family 10 member 7 (SLC10A7), t - Nucleotide

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Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine. [Orphanet J Rare Dis. 2023]
Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine.
Zhang W, Yao Z, Guo R, Cao J, Li W, Hao C, Zhang X. Orphanet J Rare Dis. 2023 Nov 30; 18(1):371. Epub 2023 Nov 30.
SLC10A7, an orphan member of the SLC10 family involved in congenital disorders of glycosylation. [Hum Genet. 2022]
SLC10A7, an orphan member of the SLC10 family involved in congenital disorders of glycosylation.
Durin Z, Dubail J, Layotte A, Legrand D, Cormier-Daire V, Foulquier F. Hum Genet. 2022 Jul; 141(7):1287-1298. Epub 2022 Jan 8.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.

RefSeq protein product
See the reference protein sequence for sodium/bile acid cotransporter 7 isoform X4 (XP_054206950.1).

PREDICTED: Homo sapiens solute carrier family 10 member 7 (SLC10A7), transcript ...
PREDICTED: Homo sapiens solute carrier family 10 member 7 (SLC10A7), transcript variant X7, mRNA
gi|2462599175|ref|XM_054350975.1|

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