Type | Description |
---|---|
Definition | myomesin 3 |
Date | Results | Publications |
---|---|---|
2018-08-25 11:14:00 | mutations in Pakistani patients with dilated cardiomyopathy rs375563861 (C2orf40), rs143187236 (MYOM3), and rs564181443 (RTKN2) have 3 fold or higher allele frequency in South Asians than in the global populations | 29886034 |
2016-05-14 10:45:00 | MYOM3 fragments hold promise for minimally invasive assessment of experimental therapies for DMD and other neuromuscular disorders. | 26060189 |
2009-03-25 21:36:00 | Observational study of gene-disease association. (HuGE Navigator) | 19023099 |
2008-12-03 21:30:00 | Observational study of gene-disease association. (HuGE Navigator) | 17975119 |
Type | IDs |
---|---|
Gene |
UniProtKB-ID:
MYOM3_HUMAN
UniprotKB:
Q5VTT5
UniParc:
UPI00016428D7,
UPI0000203A5D,
UPI0000458AA0
EMBL:
CH471134,
BC067101,
BX647455,
AL591178,
AK128233,
AK093280,
BC014671,
BX647453,
BX537911
Ensembl:
ENSG00000142661
KO:
hsa:127294
|
Nucleutide sequences |
EMBL-CDS:
EAW95108.1,
AAH67101.1,
CAH10377.1,
BAC87343.1,
BAC04119.1,
AAH14671.1,
CAD97895.1,
CAH10376.1
Ensembl_TRS:
ENST00000338909,
ENST00000374434
|
Protein sequencees |
Ensembl_PRO:
ENSP00000363557,
ENSP00000342689
RefSeq:
NP_689585.3
|
Others |
UniRef100:
UniRef100_Q5VTT5
UniRef90:
UniRef90_Q5VTT5
UniRef50:
UniRef50_Q5VTT5
UniGene:
Hs.523413
CCDS:
CCDS41281.1
|
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Refseq |
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