Gene

IFT140

HGNC: HGNC:29077 | GeneCards: IFT140
Saudi human-genetics coreAll Saudi-affiliated records

Overview

Approved name
Cytogenetic location
-
Locus type
-
In SaudiVarKB
4 articles, 4 mentions

Synonyms

None recorded

External resources

ClinVar ↗PubMed ↗
4Publications5Co-reported phenotypes1Reported variants
0ClinVar pathogenic / likely pathogenic
0Saudi regions
OpenLiterature network

Co-reported phenotypes

Phenotypes named in the same articles as IFT140. Co-mention, not a proven association.

PhenotypeArticlesEvidence
retinal dystrophy3View sentences
developmental delay2View sentences
Bardet-Biedl syndrome1View sentences
Leber congenital amaurosis1View sentences
renal failure1View sentences

Reported variants

Variants linked to IFT140 through dbSNP or LitVar2. ClinVar status is shown for core-subset variants.

VariantrsIDArticlesClinVar
p.Glu664Lys-2-

Saudi regions

Regions or cities named in the abstracts of articles that mention IFT140.

No Saudi region named.