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STRs in panel
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Inborn errors of metabolism

Gene: ANO10

Green List (high evidence)

ANO10 (anoctamin 10)
EnsemblGeneIds (GRCh38): ENSG00000160746
EnsemblGeneIds (GRCh37): ENSG00000160746
OMIM: 613726, Gene2Phenotype
ANO10 is in 10 panels

3 reviews

Zornitza Stark (Australian Genomics)

Red List (low evidence)

Definitely a green gene, but the link to mitochondrial function/disease seems indirect.
Created: 27 Aug 2018, 8:45 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Ellen McDonagh (Genomics England Curator)

Comment on list classification: Seems to be strong evidence for association with Spinocerebellar ataxia, and green review from expert.
Created: 26 Feb 2016, 12:11 p.m.

Shamima Rahman (UCL Institute of Child Health)

Green List (high evidence)

History Filter Activity

8 Jan 2019, Gel status: 4

Panel promoted to version 1.0

Ellen McDonagh (Genomics England Curator)

Checked against super panel made up of the panel constituents. Ready to promote to version 1.

16 Dec 2018, Gel status: 4

Set Phenotypes

Ellen McDonagh (Genomics England Curator)

Added phenotypes Spinocerebellar ataxia, autosomal recessive 10, 613728 for gene: ANO10

16 Dec 2018, Gel status: 4

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

Ellen McDonagh (Genomics England Curator)

gene: ANO10 was added gene: ANO10 was added to Inborn errors of metabolism. Sources: Expert Review Green Mode of inheritance for gene: ANO10 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ANO10 were set to Spinocerebellar ataxia, autosomal recessive 10, 613728