Bos taurus Gene: MYO1C
Summary
InnateDB Gene IDBG-632689.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MYO1C
Gene Name Unconventional myosin-Ic
Synonyms MMIb
Species Bos taurus
Ensembl Gene ENSBTAG00000001332
Encoded Proteins
Myosin-Ic
Myosin-Ic
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 ENSG00000197879:
This gene encodes a member of the unconventional myosin protein family, which are actin-based molecular motors. The protein is found in the cytoplasm, and one isoform with a unique N-terminus is also found in the nucleus. The nuclear isoform associates with RNA polymerase I and II and functions in transcription initiation. The mouse ortholog of this protein also functions in intracellular vesicle transport to the plasma membrane. Multiple transcript variants encoding different isoforms have been found for this gene. The related gene myosin IE has been referred to as myosin IC in the literature, but it is a distinct locus on chromosome 19. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 19:23168435-23191280
Strand Reverse strand
Band
Transcripts
ENSBTAT00000029555 ENSBTAP00000029554
ENSBTAT00000029554 ENSBTAP00000029553
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 44 interaction(s) predicted by orthology.
Predicted by orthology
Total 44 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0003774 motor activity
GO:0003779 actin binding
GO:0005102 receptor binding
GO:0005515 protein binding
GO:0005516 calmodulin binding
GO:0005524 ATP binding
GO:0008022 protein C-terminus binding
Biological Process
GO:0006605 protein targeting
GO:0006612 protein targeting to membrane
GO:0006810 transport
GO:0008152 metabolic process
GO:0015031 protein transport
GO:0030335 positive regulation of cell migration
GO:0038089 positive regulation of cell migration by vascular endothelial growth factor signaling pathway
GO:0051028 mRNA transport
GO:0090314 positive regulation of protein targeting to membrane
GO:1900748 positive regulation of vascular endothelial growth factor signaling pathway
GO:2000810 regulation of tight junction assembly
Cellular Component
GO:0001726 ruffle
GO:0005634 nucleus
GO:0005643 nuclear pore
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005886 plasma membrane
GO:0005902 microvillus
GO:0005903 brush border
GO:0009925 basal plasma membrane
GO:0016020 membrane
GO:0016023 cytoplasmic membrane-bounded vesicle
GO:0016328 lateral plasma membrane
GO:0016459 myosin complex
GO:0031410 cytoplasmic vesicle
GO:0031941 filamentous actin
GO:0032420 stereocilium
GO:0042995 cell projection
GO:0045121 membrane raft
GO:0045160 myosin I complex
GO:0060171 stereocilium membrane
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
Fcgamma receptor (FCGR) dependent phagocytosis pathway
Translocation of GLUT4 to the plasma membrane pathway
Immune System pathway
Regulation of actin dynamics for phagocytic cup formation pathway
Innate Immune System pathway
Membrane Trafficking pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Regulation of actin dynamics for phagocytic cup formation pathway
Translocation of GLUT4 to the plasma membrane pathway
Innate Immune System pathway
Immune System pathway
Fcgamma receptor (FCGR) dependent phagocytosis pathway
Membrane Trafficking pathway
Innate Immune System pathway
Regulation of actin dynamics for phagocytic cup formation pathway
Membrane Trafficking pathway
Immune System pathway
Fcgamma receptor (FCGR) dependent phagocytosis pathway
Translocation of GLUT4 to the plasma membrane pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Bt.4957
RefSeq NM_174396 XM_005220064 XM_005220065
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas