IFT74 gene

intraflagellar transport 74

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

This gene encodes a core intraflagellar transport (IFT) protein which belongs to a multi-protein complex involved in the transport of ciliary proteins along axonemal microtubules. IFT proteins are found at the base of the cilium as well as inside the cilium, where they assemble into long arrays between the ciliary base and tip. This protein, together with intraflagellar transport protein 81, binds and transports tubulin within cilia and is required for ciliogenesis. Naturally occurring mutations in this gene are associated with amyotrophic lateral sclerosis--frontotemporal dementia and Bardet-Biedl Syndrome. [provided by RefSeq, Mar 2017]

From UniProt:

Component of the intraflagellar transport (IFT) complex B: together with IFT81, forms a tubulin-binding module that specifically mediates transport of tubulin within the cilium. Binds beta-tubulin via its basic region. Required for ciliogenesis.

From NCBI Gene:

  • Bardet-Biedl syndrome 20

From UniProt:

Bardet-Biedl syndrome 20 (BBS20): A form of Bardet-Biedl syndrome, a syndrome characterized by usually severe pigmentary retinopathy, early-onset obesity, polydactyly, hypogenitalism, renal malformation and mental retardation. Secondary features include diabetes mellitus, hypertension and congenital heart disease. Bardet-Biedl syndrome inheritance is autosomal recessive, but three mutated alleles (two at one locus, and a third at a second locus) may be required for clinical manifestation of some forms of the disease. [MIM:617119]

Cytogenetic Location: 9p21.2, which is the short (p) arm of chromosome 9 at position 21.2

Molecular Location: base pairs 26,947,039 to 27,066,129 on chromosome 9 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 9p21.2, which is the short (p) arm of chromosome 9 at position 21.2
  • BBS20
  • CCDC2
  • CMG-1
  • CMG1