Type | Description |
---|---|
Definition | myosin heavy chain 8 |
Date | Results | Publications |
---|---|---|
2021-04-03 13:31:00 | Novel MYH8 mutations in 152 Han Chinese samples with ovarian endometriosis. | 32308057 |
2021-03-13 13:26:00 | Novel exomic rare variants associated with venous thrombosis. | 32232851 |
2020-10-31 13:12:00 | Truncation of MYH8 tail in AML: a novel prognostic marker with increase cell migration and epithelial-mesenchymal transition utilizing RAF/MAPK pathway. | 31430364 |
2018-05-05 10:08:00 | There was an immediate shutdown of the MHC IIX gene after resistance exercise. Silencing of the MHC IIX gene is sustained at least 4 days after removal of the stimulus. | 28508505 |
2017-08-12 10:31:00 | Loss-of-function variants in the MYH8 gene do not cause autosomal dominant trismus-pseudocamptodactyly syndrome. | 28377322 |
Type | IDs |
---|---|
Synonymous | DA7, MyHC-peri, MyHC-pn, gtMHC-F |
Gene |
UniProtKB-ID:
MYH8_HUMAN
UniprotKB:
P13535
UniParc:
UPI000012FB7D
EMBL:
Z38133,
AF067143,
X51592,
M36769
Ensembl:
ENSG00000133020
KO:
hsa:4626
|
Nucleutide sequences |
EMBL-CDS:
AAC17185.1,
CAA35941.1,
AAC21557.1,
CAA86293.1
Ensembl_TRS:
ENST00000403437
|
Protein sequencees |
Ensembl_PRO:
ENSP00000384330
RefSeq:
NP_002463.2
|
Others |
UniRef100:
UniRef100_P13535
UniRef90:
UniRef90_P13535
UniRef50:
UniRef50_P13535
UniGene:
Hs.700484
CCDS:
CCDS11153.1
|
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---|---|---|---|---|---|---|---|---|
Refseq |
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