AutismKB 2.0

Annotation Detail for MYH8


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Basic Information Top
Gene Symbol:MYH8 ( MyHC-peri,MyHC-pn,gtMHC-F )
Gene Full Name: myosin, heavy chain 8, skeletal muscle, perinatal
Band: 17p13.1
Quick LinksEntrez ID:4626; OMIM: 160741; Uniprot ID:MYH8_HUMAN; ENSEMBL ID: ENSG00000133020; HGNC ID: 7578
Relate to Another Database: SFARIGene; denovo-db
Related Pathway Information Top
No data
Pathway IDPathway Name
hsa05416Viral myocarditis
hsa04530Tight junction
Pathway IDPathway Name
Muscle contraction
No data
Pathway IDPathway Name
P00044Nicotinic acetylcholine receptor signaling pathway
P00016Cytoskeletal regulation by Rho GTPase
P00031Inflammation mediated by chemokine and cytokine signaling pathway
P00057Wnt signaling pathway
No data
Related Diseases/Disorders Top
No data
Desease IDDesease Name
2042Thrombophlebitis
No data
No data
Desease Name
Carney complex variant
Trismus-pseudocamptodactyly syndrome
Comparative Toxicogenomics Database Top
Chemical ID Chemical Name Interaction Interaction Action Publication
D005419 Flavonoids Flavonoids results in increased expression of MYH8 mRNAincreases expression 18035473
Disease ID Disease Name Direct Evidence Inference Chemical Name Inference Score Publication
OMIM:608837 CARNEY COMPLEX VARIANT marker/mechanism
MESH:D007249 Inflammation Flavonoids 2.8817296493
OMIM:158300 TRISMUS-PSEUDOCAMPTODACTYLY SYNDROME marker/mechanism
Pathway ID Pathway Name
REACT:17044 Muscle contraction
KEGG:04530 Tight junction
KEGG:05416 Viral myocarditis
Pharmacogenomics Knowledge Base Top
Drug Bank Top

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  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018


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