Possible mitochondrial disorder - nuclear genes
Gene: SRRT

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

3 reviews

Ivone Leong (Genomics England Curator)

Red List (low evidence)

Initial gene list and info collated by Carl Fratter (Oxford University Hospitals NHS Trust) January 2019 on behalf of the GMS Mitochondrial specialist test group.
Created: 4 Feb 2019, 1:36 p.m.

Mode of inheritance
Unknown

Phenotypes
No OMIM phenotype

Created: 4 Feb 2019, 1:36 p.m.

Panel version: 0.5

Shamima Rahman (UCL Institute of Child Health)

Red List (low evidence)

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

Created: 6 Feb 2016, 11:46 p.m.

Panel version: Imported from Mitochondrial disorders panel version 0.16

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.

Created: 1 Jul 2015, 10:39 a.m.

Panel version: Imported from Mitochondrial disorders panel version 0

Details

Mode of Inheritance

Unknown

Sources

NHS GMS
Expert Review Red

Phenotypes

No OMIM phenotype

OMIM

614469

Clinvar variants

Variants in SRRT

Penetrance

None

Panels with this gene

History Filter Activity

4 Feb 2019, Gel status: 1

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

Ivone Leong (Genomics England Curator)

gene: SRRT was added gene: SRRT was added to Possible mitochondrial disorder - nuclear genes. Sources: Expert Review Red,NHS GMS Mode of inheritance for gene: SRRT was set to Unknown Phenotypes for gene: SRRT were set to No OMIM phenotype

Possible mitochondrial disorder - nuclear genes Gene: SRRT