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Mendeliome

Gene: STK33

Red List (low evidence)

STK33 (serine/threonine kinase 33)
EnsemblGeneIds (GRCh38): ENSG00000130413
EnsemblGeneIds (GRCh37): ENSG00000130413
OMIM: 607670, Gene2Phenotype
STK33 is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Four brothers with a homozygous variant and an animal model.
Sources: Literature
Created: 7 Jun 2024, 12:20 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Spermatogenic failure 93, MIM#620849

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Spermatogenic failure 93, MIM#620849
OMIM
607670
Clinvar variants
Variants in STK33
Penetrance
None
Publications
Panels with this gene

History Filter Activity

7 Jun 2024, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: stk33 has been classified as Red List (Low Evidence).

7 Jun 2024, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: STK33 was added gene: STK33 was added to Mendeliome. Sources: Literature Mode of inheritance for gene: STK33 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: STK33 were set to 34155512; 29155043 Phenotypes for gene: STK33 were set to Spermatogenic failure 93, MIM#620849 Review for gene: STK33 was set to RED