Type | Description |
---|---|
Definition | xin actin binding repeat containing 1 |
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 |
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
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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