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Mendeliome

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

No evidence for Mendelian gene-disease association.
Created: 18 May 2022, 7:47 a.m. | Last Modified: 18 May 2022, 7:47 a.m.
Panel Version: 0.14504

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Tags
non-coding gene
OMIM
611607
Clinvar variants
Variants in MIR182
Penetrance
None
Panels with this gene

History Filter Activity

14 Mar 2025, Gel status: 1

Added Tag

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Tag non-coding gene tag was added to gene: MIR182.

18 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: mir182 has been classified as Red List (Low Evidence).

18 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: mir182 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: MIR182 was added gene: MIR182 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: MIR182 was set to Unknown