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BabyScreen+ newborn screening

Gene: ST14

Red List (low evidence)

ST14 (suppression of tumorigenicity 14)
EnsemblGeneIds (GRCh38): ENSG00000149418
EnsemblGeneIds (GRCh37): ENSG00000149418
OMIM: 606797, Gene2Phenotype
ST14 is in 5 panels

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Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Ichthyosis hypotrichosis syndrome
OMIM
606797
Clinvar variants
Variants in ST14
Penetrance
None
Panels with this gene

History Filter Activity

28 Jul 2024, Gel status: 1

Set Phenotypes

Tommy Li (Murdoch Children's Research Institute)

Added phenotypes Ichthyosis hypotrichosis syndrome for gene: ST14

18 Sep 2022, Gel status: 1

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: ST14 was added gene: ST14 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: ST14 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ST14 were set to Ichthyosis hypotrichosis syndrome