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  3. MT-RNR2
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Mitochondrial disease

Gene: MT-RNR2

Red List (low evidence)
MT-RNR2 (mitochondrially encoded 16S RNA)
EnsemblGeneIds (GRCh38): ENSG00000210082
EnsemblGeneIds (GRCh37): ENSG00000210082
OMIM: 561010, Gene2Phenotype
MT-RNR2 is in 1 panel

1 review

Chern Lim (Victorian Clinical Genetics Services)

Red List (low evidence)

Disease association not established (PMID:29233888 and in-house expert review).
Sources: Expert Review, Literature
Created: 21 Aug 2020, 12:19 a.m.

Mode of inheritance
MITOCHONDRIAL

Publications

Created: 21 Aug 2020, 12:19 a.m.

Panel version: 0.459

Details

Mode of Inheritance
MITOCHONDRIAL
Sources
  • Expert Review Red
OMIM
561010
Clinvar variants
Variants in MT-RNR2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

21 Aug 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: mt-rnr2 has been classified as Red List (Low Evidence).

21 Aug 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: mt-rnr2 has been classified as Red List (Low Evidence).

21 Aug 2020, Gel status: 0

Created, Added New Source, Set mode of inheritance, Set publications

Chern Lim (Victorian Clinical Genetics Services)

gene: MT-RNR2 was added gene: MT-RNR2 was added to Mitochondrial disease. Sources: Expert Review,Literature Mode of inheritance for gene gene: MT-RNR2 was set to MITOCHONDRIAL Publications for gene: MT-RNR2 were set to 29233888 Review for gene: MT-RNR2 was set to RED