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8997 KALRN

8997

KALRN

kalirin RhoGEF kinase

protein-coding

Homo sapiens

基因描述

Type Description
Definition kalirin RhoGEF kinase

研究结论

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

名称对应

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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