| MYO5C |
| LOCUS ID | 55930 | ||||||||||
| GENE_SYMBOL | MYO5C | ||||||||||
| GENE NAME | myosin VC | ||||||||||
| SYNONYMNS | NA | ||||||||||
| CHROMOSOME | 15 | ||||||||||
| HOMOLOGENE ID | 135711 |
| microRNAs | NA | NA |
| GENE SUMMARY |
|---|
| MYO5C (Myosin VC) is a Protein Coding gene. Diseases associated with MYO5C include Griscelli Syndrome, Type 1 and Diarrhea 2, With Microvillus Atrophy. Among its related pathways are PAK Pathway and RhoGDI Pathway. Gene Ontology (GO) annotations related to this gene include actin binding and actin filament binding. An important paralog of this gene is MYO5A. |
| OBSERVATIONS |
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| Complication | Evidence | PMID |
| Retinopathy | 1. The MYO5C related SNP (rs3751624)*A related genotype/allele and haplotype (G-A-G-G-T-G) might be associated with susceptibility for retinopathy in T2D individuals. Some chromosome 15q21-22* related genetic variations might contribute to the pathogenesis of DR. " | 22409602 |