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