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IFT172


Official Full Name
intraflagellar transport 172
Organism
Homo sapiens
Gene ID
26160
Background
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. [provided by RefSeq, Mar 2014]
Synonyms
SLB; wim; RP71; BBS20; osm-1; NPHP17; SRTD10

Cat.No. Product Name Price
SHH317269 shRNA set against Human Ift172 (NM_015662.1) Inquiry
SHH317273 shRNA set against Mouse Ift172 (NM_026298.5) Inquiry
SHH317277 shRNA set against Rat Ift172 (NM_053792.1) Inquiry
SHR082368 shRNA set against Human IFT172(NM_015662.1) Inquiry
SHW006347 shRNA set against Danio rerio IFT172 (NM_001002312) Inquiry
Cat.No. Product Name Price
CDFH009026 Human IFT172 cDNA Clone(NM_015662.1) Inquiry
CDFR013535 Rat Ift172 cDNA Clone(NM_053792.1) Inquiry
MiUTR1H-04825 IFT172 miRNA 3'UTR clone Inquiry
MiUTR1R-07358 IFT172 miRNA 3'UTR clone Inquiry
CDCB167822 Danio rerio IFT172 ORF Clone (NM_001002312) Inquiry
CDCB188752 Rabbit IFT172 ORF clone (XM_002709949.2) Inquiry
CDCL119633 Human IFT172 ORF clone (NM_015662.1) Inquiry
CDCR258465 Mouse Ift172 ORF Clone(NM_026298.5) Inquiry
CDCR380567 Rat Ift172 ORF Clone(NM_053792.1) Inquiry
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