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8034 SLC25A16

8034

SLC25A16

solute carrier family 25 member 16

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 25 member 16

研究结论

Date Results Publications
2019-04-27 10:48:00 The authors findings report an extreme rare missense mutation in SLC25A1 which supports the causality of this variant for autosomal recessive form of isolated fingernail dysplasia. 28504827
2013-07-02 10:26:00 Compares and contrasts all the known human SLC25A* genes and includes functional information. 23266187
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20877624
2010-06-30 22:05:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614
2009-12-02 21:41:00 Observational study of gene-disease association. (HuGE Navigator) 16385451

名称对应

Type IDs
Synonymous D10S105E, GDA, GDC, HGT.1, ML7, hML7
Gene
UniProtKB-ID: GDC_HUMAN, B4DPV4_HUMAN, B4DHV9_HUMAN
UniprotKB: P16260, B4DPV4, B4DHV9
UniParc: UPI000041AE1F, UPI00000704FB, UPI00017A70DC
EMBL: AK290255, M31659, AK295287, AK298510, CH471083, AL713888, BC030266
Ensembl: ENSG00000122912
KO: hsa:8034
Nucleutide sequences
EMBL-CDS: AAA36329.1, EAW54298.1, BAF82944.1, AAH30266.1, BAG60716.1, BAG58271.1
Ensembl_TRS: ENST00000609923
Protein sequencees
Ensembl_PRO: ENSP00000476815
RefSeq: NP_001311244.1, NP_001311243.1, NP_689920.1, NP_001311241.1, NP_001311246.1, NP_001311242.1
Others
UniRef100: UniRef100_B4DHV9, UniRef100_P16260
UniRef90: UniRef90_P16260, UniRef90_B4DHV9
UniRef50: UniRef50_P16260
UniGene: Hs.180408
CCDS: CCDS7280.1

全选

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研究热度

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