Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Hearing loss

Gene: MOS

Red List (low evidence)

MOS (MOS proto-oncogene, serine/threonine kinase)
EnsemblGeneIds (GRCh38): ENSG00000172680
EnsemblGeneIds (GRCh37): ENSG00000172680
OMIM: 190060, Gene2Phenotype
MOS is in 1 panel

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

MOS is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:07 a.m.
MOS is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:43 p.m.

Publications

Details

Sources
  • Expert
OMIM
190060
Clinvar variants
Variants in MOS
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

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