This Panel is marked as Deleted
Immunological disorders_SuperPanel_PanelAppAustralia
Gene: SLC37A4
SLC37A4 (solute carrier family 37 member 4)
EnsemblGeneIds (GRCh38): ENSG00000137700
EnsemblGeneIds (GRCh37): ENSG00000137700
OMIM: 602671, Gene2Phenotype
SLC37A4 is in 14 panels
EnsemblGeneIds (GRCh38): ENSG00000137700
EnsemblGeneIds (GRCh37): ENSG00000137700
OMIM: 602671, Gene2Phenotype
SLC37A4 is in 14 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 602671
- Clinvar variants
- Variants in SLC37A4
- Penetrance
- None
- Panels with this gene
-
- Likely inborn error of metabolism
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Cytopenia - NOT Fanconi anaemia
- COVID-19 research
- Undiagnosed metabolic disorders
- Ketotic hypoglycaemia
- Fetal anomalies
- DDG2P
- Glycogen storage disease
- Hyperammonaemia
- Congenital disorders of glycosylation
- Gastrointestinal epithelial barrier disorders
- Childhood onset dystonia, chorea or related movement disorder
History Filter Activity
7 Apr 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance
Rebecca Foulger (Genomics England curator)gene: SLC37A4 was added gene: SLC37A4 was added to Immunological disorders_SuperPanel_PanelAppAustralia. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: SLC37A4 was set to Unknown