Genes in panel

Likely inborn error of metabolism - targeted testing not possible

Gene: SRRT

Red List (low evidence)

SRRT (serrate, RNA effector molecule)
EnsemblGeneIds (GRCh38): ENSG00000087087
EnsemblGeneIds (GRCh37): ENSG00000087087
OMIM: 614469, Gene2Phenotype
SRRT is in 3 panels

2 reviews

Shamima Rahman (UCL Institute of Child Health)

Red List (low evidence)

no mutation reports in literature
Created: 6 Feb 2016, 11:46 p.m.

Ellen McDonagh (Genomics England Curator)

This gene was submitted as "ARS2" in the expert list, which is likely to correspond to this HGNC-approved symbol.
Created: 1 Jul 2015, 10:39 a.m.


Mode of Inheritance
  • Expert Review Red
  • Multiple respiratory chain complex deficiencies (disorders of protein synthesis)
Clinvar variants
Variants in SRRT
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 Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: SRRT was added gene: SRRT was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: SRRT was set to Unknown Phenotypes for gene: SRRT were set to Multiple respiratory chain complex deficiencies (disorders of protein synthesis)