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84976 DISP1

84976

DISP1

dispatched RND transporter family member 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition dispatched RND transporter family member 1

研究结论

Date Results Publications
2019-04-20 11:43:00 Genome-wide association study does not support the role of DISP1 in predicting serotonin reuptake inhibitor response in obsessive-compulsive disorder. 29953682
2016-10-22 10:04:00 The top single-nucleotide polymorphism (SNP) was rs17162912 (P=1.76 x 10(-8)), which is near the DISP1 gene on 1q41-q42, a microdeletion region implicated in neurological development. 25824302
2013-07-13 11:52:00 DISP-1 is required for non-small cell lung carcinoma cells proliferation 22733134
2011-06-18 11:17:00 Studies indicate that DISP1 haploinsufficiency may not be solely responsible for the major features of 1q41q42 microdeletion syndrome, and other genes in the SRO likely play a role in the phenotype. 20951845
2011-01-15 11:27:00 report of 1st de novo DISP1 point mutation in patient with congenital diaphragmatic hernia (CDH); finding with Disp1 embryonic mouse diaphragm and lung expression and previously reported 1q41q42 aberrations in CDH suggests DISP1 may be CDH candidate gene 20799323

名称对应

Type IDs
Synonymous DISPA
Gene
UniProtKB-ID: DISP1_HUMAN
UniprotKB: Q96F81
UniParc: UPI000016069D
EMBL: AK023679, AK026114, AL133092, BC007734, BC011542, AK098669
Ensembl: ENSG00000154309
KO: hsa:84976
Nucleutide sequences
EMBL-CDS: BAB15365.1, AAH07734.1, BAB14637.1, BAC05373.1, CAB61406.1, AAH11542.2
Ensembl_TRS: ENST00000284476
Protein sequencees
Ensembl_PRO: ENSP00000284476
RefSeq: NP_001364157.1, XP_011508377.1, XP_016858101.1, XP_011508375.1, NP_001364158.1, XP_016858100.1, XP_011508376.1, XP_011508374.1, NP_001337559.1, NP_116279.2, XP_006711657.1, XP_006711655.1, NP_001356523.1
Others
UniRef100: UniRef100_Q96F81
UniRef90: UniRef90_Q96F81
UniRef50: UniRef50_Q3TDN0
UniGene: Hs.528817, Hs.692324
CCDS: CCDS1536.1

全选

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