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Autism

Gene: KCNK7

Red List (low evidence)

KCNK7 (potassium two pore domain channel subfamily K member 7)
EnsemblGeneIds (GRCh38): ENSG00000173338
EnsemblGeneIds (GRCh37): ENSG00000173338
OMIM: 603940, Gene2Phenotype
KCNK7 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/KCNK7
Created: 1 Apr 2019, 11:26 a.m.

Details

Sources
OMIM
603940
Clinvar variants
Variants in KCNK7
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 KCNK7.

29 Mar 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Louise Daugherty (Genomics England Curator)

gene: KCNK7 was added gene: KCNK7 was added to Autism. Sources: SFARI Mode of inheritance for gene: KCNK7 was set to