1. Panels
  2. Cerebellar and Pontocerebellar Hypoplasia
  3. WDR91
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Cerebellar and Pontocerebellar Hypoplasia

Gene: WDR91

Red List (low evidence)
WDR91 (WD repeat domain 91)
EnsemblGeneIds (GRCh38): ENSG00000105875
EnsemblGeneIds (GRCh37): ENSG00000105875
OMIM: 616303, Gene2Phenotype
WDR91 is in 4 panels

1 review

Sebastian Lunke (Victorian Clinical Genetics Services)

Red List (low evidence)

Gene has been shown to complex with WDR81 which is involved in severe microcephaly, but no published evidence for WDR91 in patients was be identified at time of review
Created: 6 Dec 2019, 10:51 p.m. | Last Modified: 6 Dec 2019, 10:51 p.m.
Panel Version: 0.1

Mode of inheritance
Unknown

Publications

Created: 6 Dec 2019, 10:51 p.m.
Last Modified: 6 Dec 2019, 10:51 p.m.
Panel version: 0.1

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
616303
Clinvar variants
Variants in WDR91
Penetrance
None
Panels with this gene

History Filter Activity

6 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Sebastian Lunke (Victorian Clinical Genetics Services)

Gene: wdr91 has been classified as Red List (Low Evidence).

6 Dec 2019, Gel status: 3

Entity classified by Genomics England curator

Sebastian Lunke (Victorian Clinical Genetics Services)

Gene: wdr91 has been classified as Green List (High Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: WDR91 was added gene: WDR91 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: WDR91 was set to Unknown