Hydrocephalus

Gene: TBX15

Red List (low evidence)

TBX15 (T-box 15)
EnsemblGeneIds (GRCh38): ENSG00000092607
EnsemblGeneIds (GRCh37): ENSG00000092607
OMIM: 604127, Gene2Phenotype
TBX15 is in 7 panels

2 reviews

Louise Daugherty (Genomics England Curator)

I don't know

As discussed with the GMS Neurology Specialist Test Group webex call 11th July 2019: The Specialist Test Group all agreed that there is only enough evidence to rate this gene Red
Created: 29 Jul 2019, 2:49 p.m. | Last Modified: 29 Jul 2019, 2:49 p.m.
Panel Version: 1.34

Helen Brittain (Genomics England Curator)

Red List (low evidence)

No clear hydrocephalus or macrocephalic phenotype to make this relevant for inclusion
Created: 9 May 2017, 1:23 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Cousin syndrome

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Red
  • Literature
Phenotypes
  • Cousin syndrome
OMIM
604127
Clinvar variants
Variants in TBX15
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

29 Jul 2019, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source NHS GMS was added to TBX15.

31 May 2017, Gel status: 1

panel promoted to version 1

Ellen McDonagh (Genomics England Curator)

31.05.2017 - panel revised after internal curation and clinical review.

9 May 2017, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

TBX15 was added to Hydrocephaluspanel. Source: Expert Review Red

9 May 2017, Gel status: 0

Added New Source

Helen Brittain (Genomics England Curator)

TBX15 was added to Hydrocephaluspanel. Sources: Literature

9 May 2017, Gel status: 0

Created

Helen Brittain (Genomics England Curator)

TBX15 was created by helen.brittain