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Autism

Gene: CECR2

Red List (low evidence)

CECR2 (CECR2, histone acetyl-lysine reader)
EnsemblGeneIds (GRCh38): ENSG00000099954
EnsemblGeneIds (GRCh37): ENSG00000099954
OMIM: 607576, Gene2Phenotype
CECR2 is in 1 panel

1 review

Louise Daugherty (Genomics England Curator)

I don't know

Each gene in the SFARI Human Gene module has a dedicated entry summary page, see here for more info on this gene: https://gene.sfari.org/database/human-gene/CECR2
Created: 1 Apr 2019, 11:26 a.m.

Details

Sources
OMIM
607576
Clinvar variants
Variants in CECR2
Penetrance
None
Panels with this gene

History Filter Activity

29 Mar 2019, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source Expert Review Red was added to CECR2.

29 Mar 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Louise Daugherty (Genomics England Curator)

gene: CECR2 was added gene: CECR2 was added to Autism. Sources: SFARI Mode of inheritance for gene: CECR2 was set to