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Gene : MYO1C Homo sapiens

Name  ? myosin IC Cytological Location  17p13.3
Brief Description  myosin IC
Description  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]
  • synonyms:
  • OTTHUMG00000090323,
  • MYO1C,
  • uc002fso.4,
  • NMI,
  • NM_001080779,
  • HGNC:7597,
  • myr2,
  • X98507,
  • MMIb,
  • MMI-beta,
  • myr2
  • identifiers:
  • 4641,
  • ENSG00000197879,
  • MYO1C

Genome feature

Region: gene ? Length: 28501  
Location: 17:1464186-1492686 reverse strand Cyto location: 17p13.3

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

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Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



758 SN Ps

5 Cross References

17 Data Sets

20 Homologues

0 Located Features

97 Rna Seq Results