KEGG   VARIANT: 4627v1
Entry
4627v1                      Variant                                
Name
MYH9 mutation
Type
Loss of function
Gene
MYH9  myosin heavy chain 9 [KO:K10352]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 160775
Network
nt06541  Cytoskeleton in neurons
nt06546  IgSF CAM signaling
Disease
H00233  MYH9-related disease
H00604  Deafness, autosomal dominant
Reference
PMID:32545517
  Authors
Asensio-Juarez G, Llorente-Gonzalez C, Vicente-Manzanares M
  Title
Linking the Landscape of MYH9-Related Diseases to the Molecular Mechanisms that Control Non-Muscle Myosin II-A Function in Cells.
  Journal
Cells 9:cells9061458 (2020)
DOI:10.3390/cells9061458
LinkDB

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