Mus musculus Gene: Myo7a
Summary
InnateDB Gene IDBG-200041.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Myo7a
Gene Name myosin VIIA
Synonyms Hdb; Myo7; nmf371; polka; sh-1; sh1; USH1B
Species Mus musculus
Ensembl Gene ENSMUSG00000030761
Encoded Proteins
myosin VIIA
myosin VIIA
myosin VIIA
myosin VIIA
myosin VIIA
myosin VIIA
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000137474:
This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:98051060-98119524
Strand Reverse strand
Band E1
Transcripts
ENSMUST00000084979 ENSMUSP00000082046
ENSMUST00000107128 ENSMUSP00000102745
ENSMUST00000107127 ENSMUSP00000102744
ENSMUST00000107122 ENSMUSP00000102739
ENSMUST00000156992
ENSMUST00000124787
ENSMUST00000152975
ENSMUST00000153657 ENSMUSP00000114723
ENSMUST00000155637
ENSMUST00000149079
ENSMUST00000138627 ENSMUSP00000114944
ENSMUST00000131632
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 11 experimentally validated interaction(s) in this database.
They are also associated with 12 interaction(s) predicted by orthology.
Experimentally validated
Total 11 [view]
Protein-Protein 11 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 12 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000146 microfilament motor activity
GO:0003774 motor activity
GO:0003779 actin binding
GO:0005515 protein binding
GO:0005516 calmodulin binding
GO:0005524 ATP binding
GO:0019904 protein domain specific binding
GO:0030507 spectrin binding
GO:0030898 actin-dependent ATPase activity
GO:0032403 protein complex binding
GO:0042803 protein homodimerization activity
GO:0043531 ADP binding
GO:0051015 actin filament binding
Biological Process
GO:0001845 phagolysosome assembly
GO:0006200 ATP catabolic process
GO:0006886 intracellular protein transport
GO:0006909 phagocytosis
GO:0007040 lysosome organization
GO:0007600 sensory perception
GO:0007601 visual perception
GO:0007605 sensory perception of sound
GO:0008152 metabolic process
GO:0030030 cell projection organization
GO:0030048 actin filament-based movement
GO:0042472 inner ear morphogenesis
GO:0042490 mechanoreceptor differentiation
GO:0042491 auditory receptor cell differentiation
GO:0048563 post-embryonic organ morphogenesis
GO:0048839 inner ear development
GO:0050953 sensory perception of light stimulus
GO:0050957 equilibrioception
GO:0051875 pigment granule localization
GO:0051904 pigment granule transport
GO:0060088 auditory receptor cell stereocilium organization
GO:0060113 inner ear receptor cell differentiation
Cellular Component
GO:0001750 photoreceptor outer segment
GO:0001917 photoreceptor inner segment
GO:0005737 cytoplasm
GO:0005765 lysosomal membrane
GO:0005829 cytosol
GO:0005856 cytoskeleton
GO:0005902 microvillus
GO:0005938 cell cortex
GO:0016324 apical plasma membrane
GO:0016459 myosin complex
GO:0031477 myosin VII complex
GO:0032391 photoreceptor connecting cilium
GO:0032420 stereocilium
GO:0042470 melanosome
GO:0045202 synapse
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Disease pathway
The canonical retinoid cycle in rods (twilight vision) pathway
Visual phototransduction pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
The canonical retinoid cycle in rods (twilight vision) pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
Visual phototransduction pathway
Disease pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL D3YUT5
UniProt Splice Variant
Entrez Gene 17921
UniGene Mm.1403
RefSeq NM_001256081 NM_001256082 NM_001256083 NM_008663 XM_006507423 XM_006507424 XM_006507425 XM_006507426 XM_006507427 XM_006507428 XM_006507429
OMIM
CCDS CCDS40026 CCDS57563 CCDS57564 CCDS57565
HPRD
IMGT
MGI ID MGI:104510
MGI Symbol Myo7a
EMBL AC115022 AC157792
GenPept
RNA Seq Atlas 17921