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84068 SLC10A7

84068

SLC10A7

solute carrier family 10 member 7

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 10 member 7

研究结论

Date Results Publications
2021-01-09 13:28:00 The orphan solute carrier SLC10A7 is a novel negative regulator of intracellular calcium signaling. 32350310
2019-03-09 11:55:00 Mutation in SLC10A7 gene is associated with anxiety defective bone mineralization. 29878199
2019-01-12 10:44:00 SLC10A7 is involved in glycosaminoglycan synthesis and specifically in skeletal development. SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta. 30082715
2010-01-21 00:00:00 Molecular characterization and expression analysis of a novel member of the SLC10 family, SLC10A7, previously known as C4orf13, is reported 17628207
2010-01-21 00:00:00 cloning and characterization; mapped to chromosome 4q31.2 and contains 12 exons; widely expressed in human tissues 15932064

名称对应

Type IDs
Synonymous C4orf13, P7
Gene
UniProtKB-ID: NTCP7_HUMAN
UniprotKB: Q0GE19
UniParc: UPI00004C429B, UPI0000037BDC, UPI0000074176, UPI0000576505, UPI000020B548, UPI000020B547, UPI0000DD5C53
EMBL: CH471056, DQ122860, DQ871036, BC120971, AK075364, BC127627, DQ122861, BC120970, BC150308, BC023288, AL136728, BC148252, BC063471, CR933647, BC127626, AY346324
Ensembl: ENSG00000120519
KO: hsa:84068
Nucleutide sequences
EMBL-CDS: AAI20972.1, AAZ32256.1, EAX05026.1, AAH23288.1, AAI48253.1, AAI27627.1, ABI31650.1, AAI50309.1, BAC11571.1, CAB66662.2, AAH63471.1, AAI27628.1, AAZ32257.1, AAI20971.1, CAI45948.1, AAQ84722.1
Gene_ORFName: PSEC0051
Ensembl_TRS: ENST00000432059, ENST00000507030, ENST00000394059, ENST00000335472, ENST00000502607, ENST00000511374
Protein sequencees
Ensembl_PRO: ENSP00000334594, ENSP00000411297, ENSP00000422577, ENSP00000421603, ENSP00000377623, ENSP00000421275
RefSeq: XP_011530616.1, NP_001025169.1, NP_115504.1, NP_001304745.1, NP_001304747.1, NP_001304746.1, XP_016864178.1, XP_011530613.1, XP_016864179.1, XP_011530615.1, NP_001287771.1, XP_016864181.1, XP_016864180.1
Others
UniRef100: UniRef100_Q0GE19
UniRef90: UniRef90_Q0GE19
UniRef50: UniRef50_Q0GE19
UniGene: Hs.659209
CCDS: CCDS3768.1, CCDS82963.1, CCDS82962.1, CCDS34073.1, CCDS75198.1, CCDS82964.1

全选

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