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C14ORF179


Official Full Name
intraflagellar transport 43
Organism
Homo sapiens
Gene ID
112752
Background
This gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
Synonyms
IFT43; CED3; RP81; SRTD18; C14orf179

Cat.No. Product Name Price
SHG115255 shRNA set against Human C14orf179(NM_052873.2) Inquiry
SHH317301 shRNA set against Human Ift43 (NM_052873.2) Inquiry
Cat.No. Product Name Price
CDCR036724 Human IFT43 ORF clone (NM_052873.2) Inquiry
CDFH009031 Human IFT43 cDNA Clone(NM_001102564.1) Inquiry
CDFR009846 Rat Ift43 cDNA Clone(NM_001134525.1) Inquiry
MiUTR1H-01112 IFT43 miRNA 3'UTR clone Inquiry
MiUTR3H-13124 IFT43 miRNA 3'UTR clone Inquiry
CDCB181366 Rabbit IFT43 ORF clone (XM_008272014.1) Inquiry
CDCR036722 Human IFT43 ORF clone (NM_001102564.1) Inquiry
CDCR376885 Rat Ift43 ORF Clone(NM_001134525.1) Inquiry
CDCS418732 Human IFT43 ORF Clone (BC010436) Inquiry
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