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Hearing loss

Gene: MYO1C

Red List (low evidence)

MYO1C (myosin IC)
EnsemblGeneIds (GRCh38): ENSG00000197879
EnsemblGeneIds (GRCh37): ENSG00000197879
OMIM: 606538, Gene2Phenotype
MYO1C is in 1 panel

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

MYO1C is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:07 a.m.
MYO1C is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:44 p.m.

Publications

Details

Sources
  • Expert
OMIM
606538
Clinvar variants
Variants in MYO1C
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

MYO1C was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert