Homo sapiens Gene:
MYH7
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InnateDB Gene
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IDBG-3295.5
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Last Modified
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2012-02-14 [Report errors or provide feedback]
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Gene Symbol
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MYH7
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Gene Name
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myosin, heavy chain 7, cardiac muscle, beta
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Synonyms
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CMD1S;
CMH1;
MPD1;
MYHCB;
SPMD;
SPMM
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Species
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Homo sapiens
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Ensembl Gene
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ENSG00000092054
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Encoded Proteins
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IDBP-3299
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myosin, heavy chain 7, cardiac muscle, beta
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| Summary |
Muscle myosin is a hexameric protein containing 2 heavy chain subunits, 2 alkali light chain subunits, and 2 regulatory light chain subunits. This gene encodes the beta (or slow) heavy chain subunit of cardiac myosin. It is expressed predominantly in normal human ventricle. It is also expressed in skeletal muscle tissues rich in slow-twitch type I muscle fibers. Changes in the relative abundance of this protein and the alpha (or fast) heavy subunit of cardiac myosin correlate with the contractile velocity of cardiac muscle. Its expression is also altered during thyroid hormone depletion and hemodynamic overloading. Mutations in this gene are associated with familial hypertrophic cardiomyopathy, myosin storage myopathy, dilated cardiomyopathy, and Laing early-onset distal myopathy. [provided by RefSeq, Jul 2008]
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| Type |
Protein coding
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Genomic Location
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Chromosome 14:
23881947-23904927
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Strand
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Reverse strand
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Band
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q11.2
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Transcripts
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Number of Interactions
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This gene and/or its encoded proteins are associated with 6 experimentally validated interaction(s) in this database.
| Experimentally validated |
| Total |
6
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[view]
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| Protein‑Protein |
6
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| Protein‑DNA |
0 |
| Protein‑RNA |
0 |
| DNA-DNA |
0 |
| RNA-RNA |
0 |
| DNA-RNA |
0 |
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| Molecular Function |
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| Biological Process |
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| Cellular Component |
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| Species |
Mus musculus
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Bos taurus
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| Gene ID |
Gene Order |
Method |
Confidence |
Comments |
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ENSMUSG00000053093
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Ortholuge
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Non-SSD Ortholog
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Possible paralog/unusual divergence/ gene prediction error
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ENSBTAG00000009703
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Not yet available
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Ortholuge
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Non-SSD Ortholog
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Possible paralog/unusual divergence/ gene prediction error
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| NETPATH |
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| REACTOME |
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| KEGG |
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hsa05410
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Hypertrophic cardiomyopathy (HCM) |
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| INOH |
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| PID BIOCARTA |
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| PID NCI |
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SwissProt
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P12883
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TrEMBL
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A6N930
A6N931
A8CLL2
A8CLN2
Q59EV3
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UniProt Splice Variant
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Entrez Gene
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4625
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UniGene
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Hs.655129
Hs.719946
Hs.733442
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RefSeq
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NM_000257
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HUGO
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7577
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OMIM
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160760
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CCDS
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CCDS9601
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| HPRD |
01175
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IMGT
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EMBL
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AB209708
AJ238393
BC112171
BC112173
CH471078
EF179180
EF630363
EF630364
EF630365
EF630367
EU091312
EU091313
EU091314
EU091315
EU091316
EU747717
M17712
M21665
M25133
M25134
M25135
M27636
M57965
M58018
X03741
X04627
X04628
X04629
X04630
X04631
X04632
X04633
X05631
X06976
X51591
X52889
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GenPept
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AAA36343
AAA36345
AAA51837
AAA60384
AAA62830
AAA79019
AAI12172
AAI12174
ABN05283
ABR18776
ABR18777
ABR18778
ABR18780
ABV44799
ABV44800
ABV44801
ABV44802
ABV44803
ACH92815
BAD92945
CAA27381
CAA28300
CAA29119
CAA30039
CAA35940
CAA37068
CAC20413
EAW66152
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ImmGen
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MYH7 (murine)
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RNA Seq Atlas
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4625
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