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Hearing loss

Gene: MIR183

Red List (low evidence)

MIR183 (microRNA 183)
EnsemblGeneIds (GRCh38): ENSG00000207691
EnsemblGeneIds (GRCh37): ENSG00000207691
OMIM: 611608, Gene2Phenotype
MIR183 is in 1 panel

2 reviews

Ellen McDonagh (Genomics England Curator)

Added tag to explain why there is no Ensembl gene ID for this entity.
Created: 6 Jan 2017, 3:49 p.m.

Jun Shen (Harvard Medical School)

Red List (low evidence)

MIR183 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:07 a.m.
MIR183 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:43 p.m.

Publications

Details

Sources
  • Expert
Tags
locus-type-rna-micro
OMIM
611608
Clinvar variants
Variants in MIR183
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

MIR183 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert