Gene: MYH7 (myosin, heavy chain 7, cardiac muscle, beta)  Homo sapiens

Symbol: MYH7
Name: myosin, heavy chain 7, cardiac muscle, beta
Description: 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]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: beta-myosin heavy chain; CMD1S; CMH1; DKFZp451F047; MGC138376; MGC138378; MPD1; myHC-beta; myhc-slow; MYHCB; myopathy, distal 1; myosin heavy chain (AA 1-96); myosin heavy chain 7; myosin heavy chain slow isoform; myosin heavy chain, cardiac muscle beta isoform; myosin heavy chain, polypeptide 7; myosin, heavy polypeptide 7, cardiac muscle, beta; myosin-7; OTTHUMP00000027949; rhabdomyosarcoma antigen MU-RMS-40.7A; SPMD; SPMM
Orthologs: Mus musculus : Myh7 (myosin, heavy polypeptide 7, cardiac muscle, beta)  MGI
Rattus norvegicus : Myh7 (myosin, heavy chain 7, cardiac muscle, beta)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_1144,878,931 - 4,900,476-NCBI
Human Genome Assembly HuRef143,998,386 - 4,019,919-NCBI
Human Genome Assembly GRCh371423,881,947 - 23,903,496-NCBI
Human Genome Assembly Build 361422,951,787 - 22,974,710-NCBI
Human Cytogenetic Map14q12 NCBI
Human Genome Assembly1422,951,788 - 22,974,690 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Disease Annotations
Gene-Chemical Interaction Annotations
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References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on MYH7
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
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Vista + UCSC

RGD Object Information
RGD ID: 736718
Created: 2004-02-06
Species: Homo sapiens
Last Modified: 2013-04-16
Status: ACTIVE