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Hearing loss

Gene: MIR182

Red List (low evidence)

MIR182 (microRNA 182)
EnsemblGeneIds (GRCh38): ENSG00000207990
EnsemblGeneIds (GRCh37): ENSG00000207990
OMIM: 611607, Gene2Phenotype
MIR182 is in 1 panel

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

MIR182 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:07 a.m.
MIR182 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
611607
Clinvar variants
Variants in MIR182
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

MIR182 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert