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Intellectual disability syndromic and non-syndromic

Gene: STK3

Red List (low evidence)

STK3 (serine/threonine kinase 3)
EnsemblGeneIds (GRCh38): ENSG00000104375
EnsemblGeneIds (GRCh37): ENSG00000104375
OMIM: 605030, Gene2Phenotype
STK3 is in 1 panel

1 review

Chirag Patel (Genetic Health Queensland)

Red List (low evidence)

No human phenotype.
Created: 10 Dec 2019, 11:48 a.m. | Last Modified: 10 Dec 2019, 11:48 a.m.
Panel Version: 0.1182

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Genetic Health Queensland
OMIM
605030
Clinvar variants
Variants in STK3
Penetrance
None
Panels with this gene

History Filter Activity

11 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: stk3 has been classified as Red List (Low Evidence).

10 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Chirag Patel (Genetic Health Queensland)

Gene: stk3 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: STK3 was added gene: STK3 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland Mode of inheritance for gene: STK3 was set to Unknown