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This Panel is marked as Internal

Non-Fanconi anaemia
Gene: TF

TF (transferrin)
EnsemblGeneIds (GRCh38): ENSG00000091513
EnsemblGeneIds (GRCh37): ENSG00000091513
OMIM: 190000, Gene2Phenotype
TF is in 3 panels

1 review

Mark Greenslade (Bristol Genetics Laboratory)

I don't know

Created: 5 Nov 2017, 2:40 a.m.

Panel version: 0

Details

Mode of Inheritance

BIALLELIC, autosomal or pseudoautosomal

Sources

UKGTN

OMIM

Clinvar variants

Variants in TF

Penetrance

Complete

Panels with this gene

History Filter Activity

30 Sep 2015, Gel status: 1

Set Mode of Inheritance

Ellen McDonagh (Genomics England Curator)

Model of inheritance for gene TF was set to BIALLELIC, autosomal or pseudoautosomal

30 Sep 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

TF was added to Non-Fanconi anaemiapanel. Source: UKGTN

30 Sep 2015, Gel status: 1

Set Mode of Inheritance

Ellen McDonagh (Genomics England Curator)

Model of inheritance for gene TF was set to BIALLELIC, autosomal or pseudoautosomal

30 Sep 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

TF was added to Non-Fanconi anaemiapanel. Source: UKGTN

15 Jul 2015, Gel status: 1

Set Mode of Inheritance

Ellen McDonagh (Genomics England Curator)

Model of inheritance for gene TF was changed to BIALLELIC, autosomal or pseudoautosomal

15 Jul 2015, Gel status: 1

Set Mode of Inheritance

Ellen McDonagh (Genomics England Curator)

Model of inheritance for gene TF was changed to BIALLELIC, autosomal or pseudoautosomal

15 Jul 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

TF was added to Non-Fanconi anaemiapanel. Sources: UKGTN