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165904 XIRP1

165904

XIRP1

xin actin binding repeat containing 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition xin actin binding repeat containing 1

研究结论

Date Results Publications
2019-09-28 12:37:00 Report pathogenic XIRP1/2 rare variants in arrhythmogenic disorders such as sudden unexplained nocturnal death syndrome and Brugada syndrome. 29306897
2018-01-20 10:03:00 Abnormal CMYA1 expression affects the phosphorylation of Cx43 through the protein kinase c signaling pathway, which is involved in the regulation of gap junction intercellular communication. 29176328
2015-05-16 10:32:00 Aciculin interacts with filamin C and Xin and is essential for myofibril assembly. 24963132
2014-07-05 12:46:00 The strong correlation between the degree of muscle damage and Xin immunoreactivity suggests that Xin may be a suitable outcome measure to evaluate disease progression and treatment effects in clinical trials. 24225086
2014-05-10 11:19:00 We identify the SH3 domains of nebulin and nebulette as novel ligands of proline-rich regions of Xin and XIRP2. 23985323

名称对应

Type IDs
Synonymous CMYA1, Xin
Gene
UniProtKB-ID: XIRP1_HUMAN
UniprotKB: Q702N8
UniParc: UPI00001BFB06, UPI000035CC32, UPI0000246D30
EMBL: AL713648, AK095941, BC127119, CR749430, AK096421, AJ271461, AJ626900, AJ626899, AY375160, BC139782, AK126299
Ensembl: ENSG00000168334
KO: hsa:165904
Nucleutide sequences
EMBL-CDS: CAD28459.1, AAI39783.1, AAQ64003.1, CAF25191.1, BAC04783.1, CAF25192.1, CAC81057.1, BAC86519.1, AAI27120.1, BAC04655.1, CAH18268.1
Ensembl_TRS: ENST00000421646, ENST00000396251, ENST00000340369
Protein sequencees
Ensembl_PRO: ENSP00000343140, ENSP00000379550, ENSP00000391645
RefSeq: XP_005264966.1, NP_919269.2, NP_001338306.1, NP_001185550.1
Others
UniRef100: UniRef100_Q702N8
UniRef90: UniRef90_Q702N8
UniRef50: UniRef50_Q702N8
UniGene: Hs.447868, Hs.737550
CCDS: CCDS2683.1, CCDS56245.1, CCDS87065.1

全选

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