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Autism

Gene: NIPA2

Red List (low evidence)

NIPA2 (non imprinted in Prader-Willi/Angelman syndrome 2)
EnsemblGeneIds (GRCh38): ENSG00000140157
EnsemblGeneIds (GRCh37): ENSG00000140157
OMIM: 608146, Gene2Phenotype
NIPA2 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/NIPA2
Created: 1 Apr 2019, 11:26 a.m.

Details

Sources
OMIM
608146
Clinvar variants
Variants in NIPA2
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 NIPA2.

29 Mar 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Louise Daugherty (Genomics England Curator)

gene: NIPA2 was added gene: NIPA2 was added to Autism. Sources: SFARI Mode of inheritance for gene: NIPA2 was set to