Paediatric disorders - additional genes
Gene: TLL1

TLL1 (tolloid like 1)
EnsemblGeneIds (GRCh38): ENSG00000038295
EnsemblGeneIds (GRCh37): ENSG00000038295
OMIM: 606742, Gene2Phenotype
TLL1 is in 4 panels

1 review

Ellen McDonagh (Genomics England Curator)

Red List (low evidence)

This gene was submitted by Rebecca Whittington on behalf of the South West GLH, for inclusion on the Paediatric disorders panel (https://panelapp.genomicsengland.co.uk/panels/486/) This gene is currently Red on all panels in PanelApp.
Created: 26 Nov 2019, 2:38 p.m. | Last Modified: 26 Nov 2019, 2:38 p.m.

Panel Version: 0.35

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Phenotypes
Atrial septal defect 6

Created: 26 Nov 2019, 2:38 p.m.
Last Modified: 26 Nov 2019, 2:38 p.m.
Panel version: 0.35

Details

Mode of Inheritance

MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Sources

South West GLH

Phenotypes

Atrial septal defect 6

OMIM

606742

Clinvar variants

Variants in TLL1

Penetrance

None

Panels with this gene

History Filter Activity

26 Nov 2019, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: TLL1 was added gene: TLL1 was added to Paediatric disorders - additional genes. Sources: South West GLH Mode of inheritance for gene: TLL1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: TLL1 were set to Atrial septal defect 6

Paediatric disorders - additional genes Gene: TLL1