IFT122 FISH Probe

This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Mutations in this gene cause cranioectodermal dysplasia-1. A related pseudogene is located on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
IFT122-20-RE 20 (40 μL) 200 μL color Request Pricing
IFT122-20-OR 20 (40 μL) 200 μL color Request Pricing
IFT122-20-GO 20 (40 μL) 200 μL color Request Pricing
IFT122-20-GR 20 (40 μL) 200 μL color Request Pricing
IFT122-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Mutations in this gene cause cranioectodermal dysplasia-1. A related pseudogene is located on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]

Gene Details

Gene Symbol : IFT122

Gene Name : Intraflagellar transport 122

Chromosome : CHR 3: 129,440,035-129,520,506

Locus : 3q21.3-q22.1

Alt. Genes : ENAM

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