Type | Description |
---|---|
Definition | dispatched RND transporter family member 1 |
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 |
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
|
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