Genes in panel
STRs in panel
Prev Next

Inborn errors of metabolism

Gene: SLC22A4

Red List (low evidence)

SLC22A4 (solute carrier family 22 member 4)
EnsemblGeneIds (GRCh38): ENSG00000197208
EnsemblGeneIds (GRCh37): ENSG00000197208
OMIM: 604190, Gene2Phenotype
SLC22A4 is in 3 panels

1 review

Sarah Leigh (Genomics England Curator)

Red List (low evidence)

Mode of inheritance
Unknown

Phenotypes
{Rheumatoid arthritis, susceptibility to} 180300

Publications

Details

Mode of Inheritance
Unknown
Sources
OMIM
604190
Clinvar variants
Variants in SLC22A4
Penetrance
None
Publications
Panels with this gene

History Filter Activity

8 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Ellen McDonagh (Genomics England Curator)

Sarah Leigh: Associated with phenotype in O

16 Dec 2018, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: SLC22A4 was added gene: SLC22A4 was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: SLC22A4 was set to Unknown Publications for gene: SLC22A4 were set to 24816252