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IFT88 wt Allele

Known as: hTg737, TTC10, Probe HTg737 (Polycystic Kidney Disease, Autosomal Recessive) Gene 
Human IFT88 wild-type allele is located in the vicinity of 13q12.1 and is approximately 125 kb in length. This allele, which encodes intraflagellar… 
National Institutes of Health

Papers overview

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2016
2016
DAF-19, the only RFX transcription factor found in C. elegans, is required for the formation of neuronal sensory cilia. Four… 
2015
2015
Congenital orofacial abnormalities are clinically seen in human syndromes with SHP2 germline mutations such as LEOPARD and Noonan…