Gene: KRTCAP3
Alternate names for this Gene: KCP3
Gene Summary:
Gene is located in Chromosome: 2
Location in Chromosome : 2p23.3
Description of this Gene: keratinocyte associated protein 3
Type of Gene: protein-coding
Gene: IFT172
Alternate names for this Gene: BBS20|NPHP17|RP71|SLB|SRTD10|osm-1|wim
Gene Summary: This gene encodes a subunit of the intraflagellar transport subcomplex IFT-B. Subcomplexes IFT-A and IFT-B are necessary for ciliary assembly and maintenance. Mutations in this gene have been associated with skeletal ciliopathies, with or without polydactyly, such as such short-rib thoracic dysplasias 1, 9 or 10.
Gene is located in Chromosome: 2
Location in Chromosome : 2p23.3
Description of this Gene: intraflagellar transport 172
Type of Gene: protein-coding
rs4803 in
KRTCAP3;IFT172 gene and
Arthritis, Gouty
PMID 23263486 2013 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
PMID 20884846 2010 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.
rs4803 in
KRTCAP3;IFT172 gene and
Gout
PMID 20884846 2010 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.
PMID 23263486 2013 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.