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DDG2P

Gene: TSHZ1

Red List (low evidence)

TSHZ1 (teashirt zinc finger homeobox 1)
EnsemblGeneIds (GRCh38): ENSG00000179981
EnsemblGeneIds (GRCh37): ENSG00000179981
OMIM: 614427, Gene2Phenotype
TSHZ1 is in 1 panel

1 review

Rebecca Foulger (Genomics England curator)

I don't know

Original DDG2P rating: possible.
Created: 19 Nov 2018, 11:31 a.m.

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • DD-Gene2Phenotype
  • Expert Review Red
Phenotypes
  • AURAL ATRESIA, CONGENITAL 607842
OMIM
614427
Clinvar variants
Variants in TSHZ1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

29 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Rebecca Foulger (Genomics England curator)

Rebecca Foulger: Original DDG2P rating: possibl

19 Nov 2018, Gel status: 1

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

Rebecca Foulger (Genomics England curator)

gene: TSHZ1 was added gene: TSHZ1 was added to DDG2P. Sources: Expert Review Red,DD-Gene2Phenotype Mode of inheritance for gene: TSHZ1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: TSHZ1 were set to 22152683 Phenotypes for gene: TSHZ1 were set to AURAL ATRESIA, CONGENITAL 607842