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IFT20

IFT20
Identifiers
Aliases IFT20, intraflagellar transport 20
External IDs MGI: 1915585 HomoloGene: 49559 GeneCards: IFT20
Gene location (Human)
Chromosome 17 (human)
Chr. Chromosome 17 (human)
Chromosome 17 (human)
Genomic location for IFT20
Genomic location for IFT20
Band No data available Start 28,328,325 bp
End 28,335,489 bp
RNA expression pattern
PBB GE IFT20 210312 s at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_018854

RefSeq (protein)

NP_061342

Location (UCSC) Chr 17: 28.33 – 28.34 Mb Chr 17: 78.54 – 78.54 Mb
PubMed search

NM_001267778

NM_018854

NP_777547

NP_061342

Intraflagellar transport protein 20 homolog is a protein that in humans is encoded by the IFT20 gene. The gene is composed of 6 exons and is located on human chromosome 17p11.1. This gene is expressed in human brain, lung, kidney and pancreas, and lower expression were also detected in human placenta, liver, thymus, prostate and testis.

Intraflagellar transport (IFT), in which molecular motors and IFT particle proteins participate, is very important in assembling and maintaining many cilia/flagella, such as the motile cilia that drive the swimming of cells and embryos, the nodal cilia that generate left-right asymmetry in vertebrate embryos, and the sensory cilia that detect sensory stimuli in some animals. IFT20 subunit of the particle is localized to the Golgi complex in addition to the basal body and cilia where all previous IFT particle proteins had been found. In living cells, fluorescently tagged IFT20 is highly dynamic and moves between the Golgi complex and the cilium as well as along ciliary microtubules. IFT20 has been shown to interact with SPEF2 in the testis, and plays a role in sperm motility.


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