Type | Description |
---|---|
Definition | kalirin RhoGEF kinase |
Date | Results | Publications |
---|---|---|
2020-10-03 12:56:00 | Synaptic Kalirin-7 and Trio Interactomes Reveal a GEF Protein-Dependent Neuroligin-1 Mechanism of Action. | 31801062 |
2019-10-26 12:17:00 | The interaction of kalirin with the C-terminal region of Htt influences the function of kalirin and modulates the cytotoxicity induced by C-terminal Htt. | 29789657 |
2019-06-15 11:13:00 | The data of this study reveal a novel mechanism for disease-associated single nucleotide variants of KALARN and provide a platform for modeling morphological changes in mental disorders. | 29241584 |
2018-12-22 11:57:00 | SNPs of the KALRN gene are associated with intracranial atherosclerotic stenosis in the northern Chinese population. | 30232674 |
2018-11-17 11:31:00 | Combination of polymorphisms in the NOD2, IL17RA, EPHA2 and KALRN genes could play a significant role in the development of sarcoidosis by maintaining a chronic pro-inflammatory status in macrophages | 29554915 |
Type | IDs |
---|---|
Synonymous | ARHGEF24, CHD5, CHDS5, DUET, DUO, HAPIP, TRAD |
Gene |
UniProtKB-ID:
KALRN_HUMAN,
C9IZQ6_HUMAN
UniprotKB:
O60229,
C9IZQ6
UniParc:
UPI000012C095,
UPI00001C0BD5,
UPI00001AEB7E,
UPI0000D61B68,
UPI0000457168,
UPI0000EE2103
EMBL:
BC026865,
AK125979,
BC058015,
AB011422,
AL137629,
AK131379,
U94190,
AC069233,
AC022336,
AC080008,
AC112129,
CH471052,
AC117401,
KF457679
Ensembl:
ENSG00000160145
KO:
hsa:8997
|
Nucleutide sequences |
EMBL-CDS:
AAH26865.1,
AAC15791.1,
BAD18530.1,
BAA76314.1,
EAW79410.1,
CAB70850.1,
AAH58015.1,
BAC86373.1,
EAW79423.1
Gene_ORFName:
hCG_2022551
Ensembl_TRS:
ENST00000360013,
ENST00000240874,
ENST00000291478,
ENST00000460856
|
Protein sequencees |
Ensembl_PRO:
ENSP00000291478,
ENSP00000353109,
ENSP00000240874,
ENSP00000418611
RefSeq:
XP_006713877.1,
XP_016862920.1,
NP_001375343.1,
XP_011511582.1,
XP_016862924.1,
XP_006713876.1,
NP_001309924.1,
NP_001309922.1,
XP_016862921.1,
XP_011511581.1,
NP_001375342.1,
XP_016862918.1,
NP_001309919.1,
NP_001309927.1,
NP_001309926.1,
NP_008995.2,
NP_001309918.1,
XP_016862923.1,
NP_001309928.1,
NP_001375346.1,
NP_001019831.2,
XP_006713874.1,
NP_001375345.1,
XP_011511583.1,
NP_003938.1,
NP_001309923.1,
NP_001309930.1,
NP_001309920.1,
NP_001375344.1,
NP_001375347.1,
NP_001375341.1,
XP_011511585.1,
NP_001309921.1,
XP_024309579.1,
NP_001309925.1,
XP_011511587.1,
XP_006713875.1,
NP_001375348.1,
NP_001309929.1,
NP_001309917.1,
XP_006713873.1,
XP_016862919.1
|
Others |
UniRef100:
UniRef100_C9IZQ6,
UniRef100_O60229
UniRef90:
UniRef90_P97924-6,
UniRef90_P97924
UniRef50:
UniRef50_P97924-2,
UniRef50_O75962
UniGene:
Hs.8004
CCDS:
CCDS3028.1,
CCDS3027.1
|
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Refseq |
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