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Molecular autopsy

Gene: SLC6A4

Red List (low evidence)

SLC6A4 (solute carrier family 6 member 4)
EnsemblGeneIds (GRCh38): ENSG00000108576
EnsemblGeneIds (GRCh37): ENSG00000108576
OMIM: 182138, Gene2Phenotype
SLC6A4 is in 4 panels

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Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
Phenotypes
  • Sudden infant death syndrome
OMIM
182138
Clinvar variants
Variants in SLC6A4
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 Dec 2018, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: SLC6A4 was added gene: SLC6A4 was added to Molecular autopsy. Sources: Expert Review Red Mode of inheritance for gene: SLC6A4 was set to Unknown Publications for gene: SLC6A4 were set to 12966525; 21122164 Phenotypes for gene: SLC6A4 were set to Sudden infant death syndrome