Skeletal dysplasia
Gene: IFT80EnsemblGeneIds (GRCh38): ENSG00000068885
EnsemblGeneIds (GRCh37): ENSG00000068885
OMIM: 611177, Gene2Phenotype
IFT80 is in 13 panels
4 reviews
Tracy Lester (Genetics laboratory, Oxford UK)
Cilliopathies with major skeletal involvement gp of SDs - >3 cases; Review on behalf of Tracy LesterCreated: 6 Mar 2019, 11:44 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Short-rib thoracic dysplasia 2 with or without polydactyly 611263
Eleanor Williams (Genomics England Curator)
This gene was part of an initial gene list collated by Tracy Lester, Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, February 2019 on behalf of the GMS Musculoskeletal Specialist Group; Gene symbol submitted: IFT80; Initial rating suggestion: greenCreated: 6 Mar 2019, 11:36 a.m.
Sarah Leigh (Genomics England Curator)
Listed as associated with Skeletal Dysplasia by Gene Advisor (June 2016), Steve AbbsCreated: 27 Jul 2016, 9:36 a.m.
Ana Beleza (Bristol Regional Genetics Service)
Tier 1Created: 17 Jun 2016, 8:05 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Short-rib thoracic dysplasia 2 with or without polydactyly 611263
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- NHS GMS
- Expert Review Green
- Emory Genetics Laboratory
- Radboud University Medical Center, Nijmegen
- Phenotypes
-
- Short-rib thoracic dysplasia 2 with or without polydactyly 611263
- OMIM
- 611177
- Clinvar variants
- Variants in IFT80
- Penetrance
- Complete
- Panels with this gene
-
- Ductal plate malformation
- Skeletal ciliopathies
- Limb disorders
- DDG2P
- Intellectual disability
- Fetal anomalies
- Thoracic dystrophies
- Skeletal dysplasia
- Primary ciliary disorders
- Osteogenesis imperfecta
- Clefting
- Rare multisystem ciliopathy disorders
- Childhood onset dystonia, chorea or related movement disorder
History Filter Activity
Set Phenotypes
Eleanor Williams (Genomics England Curator)Added phenotypes Short-rib thoracic dysplasia 2 with or without polydactyly 611263 for gene: IFT80
Added New Source, Status Update
Eleanor Williams (Genomics England Curator)Source NHS GMS was added to IFT80. Rating Changed from Green List (high evidence) to Green List (high evidence)
panel promoted to version 1
Sarah Leigh (Genomics England Curator)Promoted to version 1 9th August 2016
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for IFT80 were set to Short-rib thoracic dysplasia 2 with or without polydactyly 611263
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for IFT80 were set to Short-rib thoracic dysplasia 2 with or without polydactyly 611263
Set Mode of Inheritance
Sarah Leigh (Genomics England Curator)Mode of inheritance for IFT80 was changed to BIALLELIC, autosomal or pseudoautosomal
Gene classified by Genomics England curator
Sarah Leigh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
Sarah Leigh (Genomics England Curator)IFT80 was added to Unexplained skeletal dysplasiapanel. Source: Radboud University Medical Center, Nijmegen IFT80 was added to Unexplained skeletal dysplasiapanel. Source: Emory Genetics Laboratory
Created
Sarah Leigh (Genomics England Curator)IFT80 was created by sleigh
Added New Source
Sarah Leigh (Genomics England Curator)IFT80 was added to Unexplained skeletal dysplasiapanel. Sources: