Familial pulmonary fibrosis

Gene: TINF2

Green List (high evidence)

TINF2 (TERF1 interacting nuclear factor 2)
EnsemblGeneIds (GRCh38): ENSG00000092330
EnsemblGeneIds (GRCh37): ENSG00000092330
OMIM: 604319, Gene2Phenotype
TINF2 is in 21 panels

3 reviews

Louise Daugherty (Genomics England Curator)

Comment on phenotypes: Added phenotype suggested by expert reviewer
Created: 27 Apr 2017, 3:53 p.m.

Philip Molyneaux (Imperial College)

Green List (high evidence)

Associated with dyskeratosis congenita and Fibrosis
Created: 26 Apr 2017, 9:42 a.m.

Alice Gardham (Genomics England)

Green List (high evidence)

Associated with pulmonary fibrosis
Created: 9 Feb 2017, 12:09 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Dyskeratosis congenita, autosomal dominant 3 613990

Publications

History Filter Activity

27 Apr 2017, Gel status: 4

panel promoted to version 1

Louise Daugherty (Genomics England Curator)

Panel reviews were assessed, and panel was revised according to reviews and further curation. 27th April 2017

27 Apr 2017, Gel status: 4

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Phenotypes for TINF2 were set to Dyskeratosis congenita, autosomal dominant, 3, 613990; Associated with dyskeratosis congenita and Fibrosis

9 Feb 2017, Gel status: 4

Gene classified by Genomics England curator

Alice Gardham (Genomics England)

This gene has been classified as Green List (High Evidence).

9 Feb 2017, Gel status: 4

Gene classified by Genomics England curator

Alice Gardham (Genomics England)

This gene has been classified as Green List (High Evidence).

9 Feb 2017, Gel status: 0

Created

Alice Gardham (Genomics England)

TINF2 was created by agardham

9 Feb 2017, Gel status: 2

Added New Source

Alice Gardham (Genomics England)

TINF2 was added to Familial pulmonary fibrosispanel. Sources: Radboud University Medical Center, Nijmegen,Illumina TruGenome Clinical Sequencing Services,Literature