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  3. ANO5
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Acute rhabdomyolysis

Gene: ANO5

Green List (high evidence)
ANO5 (anoctamin 5)
EnsemblGeneIds (GRCh38): ENSG00000171714
EnsemblGeneIds (GRCh37): ENSG00000171714
OMIM: 608662, Gene2Phenotype
ANO5 is in 11 panels

1 review

Arina Puzriakova (Genomics England Curator)

Green List (high evidence)

This gene has been added to the panel on the recommendation of the NHS Genomic Medicine Service and should be rated green.
Created: 16 Feb 2022, 2:31 p.m. | Last Modified: 16 Feb 2022, 2:31 p.m.
Panel Version: 0.6
Created: 16 Feb 2022, 2:31 p.m.
Last Modified: 16 Feb 2022, 2:31 p.m.
Panel version: 0.6

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Muscular dystrophy, limb-girdle, autosomal recessive 12, OMIM:611307
  • Miyoshi muscular dystrophy 3, OMIM:613319
OMIM
608662
Clinvar variants
Variants in ANO5
Penetrance
None
Publications
Panels with this gene

History Filter Activity

19 Jan 2022, Gel status: 3

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

Arina Puzriakova (Genomics England Curator)

gene: ANO5 was added gene: ANO5 was added to Acute rhabdomyolysis. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: ANO5 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ANO5 were set to 25929793 Phenotypes for gene: ANO5 were set to Muscular dystrophy, limb-girdle, autosomal recessive 12, OMIM:611307; Miyoshi muscular dystrophy 3, OMIM:613319