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  3. TM6SF2
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TEST Undiagnosed metabolic disorders

Gene: TM6SF2

Red List (low evidence)
TM6SF2 (transmembrane 6 superfamily member 2)
EnsemblGeneIds (GRCh38): ENSG00000213996
EnsemblGeneIds (GRCh37): ENSG00000213996
OMIM: 606563, Gene2Phenotype
TM6SF2 is in 2 panels

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Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
OMIM
606563
Clinvar variants
Variants in TM6SF2
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: TM6SF2 was added gene: TM6SF2 was added to TEST Undiagnosed metabolic disorders. Sources: Literature Mode of inheritance for gene: TM6SF2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: TM6SF2 were set to 28235613