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321855 ift88

321855

ift88

intraflagellar transport 88 homolog

protein-coding

Danio rerio

基因描述

Type Description
Definition intraflagellar transport 88 homolog

研究结论

Date Results Publications
2011-06-04 11:30:00 Data show that IFT88 depletion induces mitotic defects in human cultured cells, in kidney cells from the IFT88 mouse mutant Tg737(orpk) and in zebrafish embryos. 21441926
2010-01-21 00:00:00 These studies reveal an essential role for IFT genes in vertebrate sensory neurons and implicate the molecular components of intraflagellar transport in degenerative disorders of these cells. 15182712
2010-01-21 00:00:00 Zebrafish IFT mutants also exhibited no dramatic changes in the craniofacial skeleton, somite formation, or motor neuron patterning. 19517571
2010-01-21 00:00:00 The functions of polaris and pkd2 in LR patterning are conserved between zebrafish and mice and that Kupffer's vesicle functions as a ciliated organ of asymmetry. 16216239

名称对应

Type IDs
Synonymous fb37b11, polaris, ttc10, wu:fb37b11, xx:zah8127
Gene
UniProtKB-ID: Q6RUQ9_DANRE
UniprotKB: Q6RUQ9
UniParc: UPI000035D962
EMBL: AY491507
KO: dre:321855
Nucleutide sequences
EMBL-CDS: AAS66768.1
Protein sequencees
RefSeq: XP_021334279.1, XP_005167585.1, XP_021334281.1, XP_021334283.1, XP_021334280.1, XP_021334282.1, XP_005167587.1, NP_001001725.1, XP_005167588.1
Others
UniRef100: UniRef100_Q6RUQ9
UniRef90: UniRef90_B0UYB0
UniRef50: UniRef50_Q13099
UniGene: Dr.2900

全选

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研究热度

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