1. Panels
  2. Renal ciliopathies
  3. IFT74
STRs in panel
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Renal ciliopathies

Gene: IFT74

Red List (low evidence)
IFT74 (intraflagellar transport 74)
EnsemblGeneIds (GRCh38): ENSG00000096872
EnsemblGeneIds (GRCh37): ENSG00000096872
OMIM: 608040, Gene2Phenotype
IFT74 is in 11 panels

1 review

Alice Gardham (Genomics England)

Red List (low evidence)

Only reported in one patient although supported by zebrafish model
Created: 25 Jan 2017, 1:11 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
?Bardet-Biedl syndrome 20 617119

Publications

Created: 25 Jan 2017, 1:11 p.m.

Panel version: Imported from Rare multisystem ciliopathy disorders panel version 0.468

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Other
Phenotypes
  • ?Bardet-Biedl syndrome 20, 617119
OMIM
608040
Clinvar variants
Variants in IFT74
Penetrance
None
Publications
Panels with this gene

History Filter Activity

10 Jul 2019, Gel status: 1

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

Eleanor Williams (Genomics England Curator)

gene: IFT74 was added gene: IFT74 was added to Renal ciliopathies. Sources: Other,Expert Review Red Mode of inheritance for gene: IFT74 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: IFT74 were set to 27486776 Phenotypes for gene: IFT74 were set to ?Bardet-Biedl syndrome 20, 617119