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  3. SLC36A2
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TEST Undiagnosed metabolic disorders

Gene: SLC36A2

Red List (low evidence)
SLC36A2 (solute carrier family 36 member 2)
EnsemblGeneIds (GRCh38): ENSG00000186335
EnsemblGeneIds (GRCh37): ENSG00000186335
OMIM: 608331, Gene2Phenotype
SLC36A2 is in 3 panels

0 reviews

Details

Mode of Inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
  • UKGTN
  • Expert Review Amber
OMIM
608331
Clinvar variants
Variants in SLC36A2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 Aug 2019, Gel status: 1

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

Sarah Leigh (Genomics England Curator)

gene: SLC36A2 was added gene: SLC36A2 was added to TEST Undiagnosed metabolic disorders. Sources: Expert Review Amber,UKGTN,Radboud University Medical Center, Nijmegen,Expert Review Red,Literature Mode of inheritance for gene: SLC36A2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: SLC36A2 were set to 27604308; 19033659