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Deafness_IsolatedAndComplex
Gene: MIR96

MIR96 (microRNA 96)
EnsemblGeneIds (GRCh38): ENSG00000199158
EnsemblGeneIds (GRCh37): ENSG00000199158
OMIM: 611606, Gene2Phenotype
MIR96 is in 5 panels

1 review

Lilian Downie (Victorian Clinical Genetics Services)

I don't know

2 families in single paper. expression studies
Created: 31 Dec 2019, 1:45 a.m. | Last Modified: 31 Dec 2019, 1:45 a.m.

Panel Version: 0.81

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Autosomal dominant hearing loss

Publications

Created: 31 Dec 2019, 1:45 a.m.
Last Modified: 31 Dec 2019, 1:45 a.m.
Panel version: 0.81

Details

Mode of Inheritance

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Sources

Expert Review Amber
Melbourne Genomics Health Alliance Deafness Flagship
Victorian Clinical Genetics Services

Phenotypes

Deafness, autosomal dominant 50, MIM# 613074

OMIM

Clinvar variants

Variants in MIR96

Penetrance

None

Publications

Panels with this gene

History Filter Activity

31 Dec 2019, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: mir96 has been classified as Amber List (Moderate Evidence).

31 Dec 2019, Gel status: 2

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: MIR96 were changed from Autosomal dominant hearing loss to Deafness, autosomal dominant 50, MIM# 613074

31 Dec 2019, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: mir96 has been classified as Amber List (Moderate Evidence).

31 Dec 2019, Gel status: 2

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: MIR96 were changed from to Autosomal dominant hearing loss

31 Dec 2019, Gel status: 2

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: MIR96 were set to

31 Dec 2019, Gel status: 2

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: MIR96 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

31 Dec 2019, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: mir96 has been classified as Amber List (Moderate Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: MIR96 was added gene: MIR96 was added to Deafness_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Deafness Flagship Mode of inheritance for gene: MIR96 was set to Unknown