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Intellectual disability syndromic and non-syndromic

Gene: XIST

Red List (low evidence)

XIST (X inactive specific transcript (non-protein coding))
EnsemblGeneIds (GRCh38): ENSG00000229807
EnsemblGeneIds (GRCh37): ENSG00000229807
OMIM: 314670, Gene2Phenotype
XIST is in 2 panels

1 review

Chirag Patel (Genetic Health Queensland)

Red List (low evidence)

Not an ID gene.
Created: 12 Feb 2020, 4:13 a.m. | Last Modified: 12 Feb 2020, 4:13 a.m.
Panel Version: 0.2135

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Genetic Health Queensland
OMIM
314670
Clinvar variants
Variants in XIST
Penetrance
None
Panels with this gene

History Filter Activity

29 May 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

12 Feb 2020, Gel status: 1

Entity classified by Genomics England curator

Chirag Patel (Genetic Health Queensland)

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

22 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: XIST was added gene: XIST was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland Mode of inheritance for gene: XIST was set to Unknown