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Mendeliome

Gene: CISH

Red List (low evidence)

CISH (cytokine inducible SH2 containing protein)
EnsemblGeneIds (GRCh38): ENSG00000114737
EnsemblGeneIds (GRCh37): ENSG00000114737
OMIM: 602441, Gene2Phenotype
CISH is in 1 panel

1 review

Ain Roesley (Victorian Clinical Genetics Services)

Red List (low evidence)

Unable to find any mendelian disease association
Created: 26 Apr 2022, 4:11 a.m. | Last Modified: 26 Apr 2022, 4:11 a.m.
Panel Version: 0.13314

Variants in this GENE are reported as part of current diagnostic practice

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
602441
Clinvar variants
Variants in CISH
Penetrance
None
Panels with this gene

History Filter Activity

26 Apr 2022, Gel status: 1

Entity classified by Genomics England curator

Ain Roesley (Victorian Clinical Genetics Services)

Gene: cish has been classified as Red List (Low Evidence).

26 Apr 2022, Gel status: 1

Entity classified by Genomics England curator

Ain Roesley (Victorian Clinical Genetics Services)

Gene: cish has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: CISH was added gene: CISH was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CISH was set to Unknown