WDR10p-L [Homo sapiens]

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A novel combination of biallelic IFT122 variants associated with cranioectodermal dysplasia: A case report. [Exp Ther Med. 2021]
A novel combination of biallelic IFT122 variants associated with cranioectodermal dysplasia: A case report.
Yang Q, Zhang Q, Chen F, Yi S, Li M, Yi S, Xu X, Luo J. Exp Ther Med. 2021 Apr; 21(4):311. Epub 2021 Feb 1.
Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene. [Neurosciences (Riyadh). 2017]
Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene.
Bhattacharjee S, Beauchamp N, Murray BE, Lynch T. Neurosciences (Riyadh). 2017 Oct; 22(4):303-307.
Beemer-Langer syndrome is a ciliopathy due to biallelic mutations in IFT122. [Am J Med Genet A. 2017]
Beemer-Langer syndrome is a ciliopathy due to biallelic mutations in IFT122.
Silveira KC, Moreno CA, Cavalcanti DP. Am J Med Genet A. 2017 May; 173(5):1186-1189. Epub 2017 Mar 28.

RefSeq genomic sequence
See the genomic reference sequence for the IFT122 gene (NG_023392.1).
RefSeq protein isoforms
See 38 reference sequence protein isoforms for the IFT122 gene.

Nucleotide
Nucleotide sequence from coding region
PubMed
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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein