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Skeletal ciliopathies

Gene: IFT27

No list
IFT27 (intraflagellar transport 27)
EnsemblGeneIds (GRCh38): ENSG00000100360
EnsemblGeneIds (GRCh37): ENSG00000100360
OMIM: 615870, Gene2Phenotype
IFT27 is in 10 panels

4 reviews

Eleanor Williams (Genomics England Curator)

Comment on list classification: Removing from the skeletal ciliopathies panel as it is covered by the Bardet Biedl syndrome panel (panel ID: 543)
Created: 28 Nov 2019, 3:30 p.m. | Last Modified: 28 Nov 2019, 3:30 p.m.
Panel Version: 0.34
Created: 28 Nov 2019, 3:30 p.m.
Last Modified: 28 Nov 2019, 3:30 p.m.
Panel version: 0.34

Rebecca Foulger (Genomics England curator)

Comment on list classification: Updated rating from Red to Amber based on presence of second paper: PMID:29704304 (2018) with ciliopathy phenotype, and added 'watchlist' tag.
Created: 1 Nov 2018, 2:49 p.m.
Aldahmesh et al. (2014, PMID:24488770) identified a homozygous c.296G-A transition in the IFT27 gene (p.C99Y) in a consanguineous family with two affected children with Bardet-Biedl syndrome-19 (MIM:615996). Additional signs in one sibling included polydactyly.

PMID:29704304 (2018) describe a fetus with an unclassified severe ciliopathy phenotype including short ribs, polydactyly, bilateral renal agenesis, and imperforate anus, with compound heterozygosity for c.118_125del, p.(Thr40Glyfs*11) and a c.352 +1G>T in IFT27.
Created: 1 Nov 2018, 2:48 p.m.
Created: 1 Nov 2018, 2:48 p.m.

Panel version: Imported from Rare multisystem ciliopathy disorders panel version 1.71

Alice Gardham (Genomics England)

Comment on list classification: Only reported in one family
Created: 23 Jan 2017, 12:02 p.m.
Created: 23 Jan 2017, 12:02 p.m.

Panel version: Imported from Rare multisystem ciliopathy disorders panel version 0.421

Caroline Wright (Genomics England Curator)

Comment on list classification: One consanguineous family in OMIM
Created: 17 Dec 2015, 2:18 p.m.
Comment on list classification: 1 family in OMIM
Created: 17 Dec 2015, 2:17 p.m.
Created: 17 Dec 2015, 2:17 p.m.

Panel version: Imported from Rare multisystem ciliopathy disorders panel version Imported from "Bardet-Biedl Syndrome" panel version 0

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Removed
  • Expert list
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • ?Bardet-Biedl syndrome 19, 615996
Tags
curated_removed
OMIM
615870
Clinvar variants
Variants in IFT27
Penetrance
None
Panels with this gene

History Filter Activity

26 Feb 2021, Gel status: 0

Added Tag

Arina Puzriakova (Genomics England Curator)

Tag curated_removed tag was added to gene: IFT27.

28 Nov 2019, Gel status: 0

Entity classified by Genomics England curator

Eleanor Williams (Genomics England Curator)

Gene: ift27 has been removed from the panel.

10 Jul 2019, Gel status: 2

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

Eleanor Williams (Genomics England Curator)

gene: IFT27 was added gene: IFT27 was added to Skeletal ciliopathies. Sources: UKGTN,Radboud University Medical Center, Nijmegen,Expert list,Expert Review Amber Mode of inheritance for gene: IFT27 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: IFT27 were set to ?Bardet-Biedl syndrome 19, 615996