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STRs in panel
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Inborn errors of metabolism

Gene: TREH

Red List (low evidence)

TREH (trehalase)
EnsemblGeneIds (GRCh38): ENSG00000118094
EnsemblGeneIds (GRCh37): ENSG00000118094
OMIM: 275360, Gene2Phenotype
TREH is in 2 panels

1 review

Helen Brittain (Genomics England Curator)

Red List (low evidence)

Trehalase deficiency unlikely to be a clinically useful phenotype. In addition no reports of variant confirmation in humans
Created: 23 Feb 2017, 5:16 p.m.

Mode of inheritance
Unknown

Phenotypes
Trehalase deficiency (Other carbohydrate disorders)

Publications

Details

Mode of Inheritance
Unknown
Sources
  • London North GLH
  • NHS GMS
  • Expert Review Red
Phenotypes
  • Trehalase deficiency (Other carbohydrate disorders)
OMIM
275360
Clinvar variants
Variants in TREH
Penetrance
None
Publications
Panels with this gene

History Filter Activity

13 Feb 2019, Gel status: 1

Added New Source, Added New Source

Ivone Leong (Genomics England Curator)

Source NHS GMS was added to TREH. Source London North GLH was added to TREH.

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, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: TREH was added gene: TREH was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: TREH was set to Unknown Publications for gene: TREH were set to 27604308 Phenotypes for gene: TREH were set to Trehalase deficiency (Other carbohydrate disorders)