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11020 IFT27

11020

IFT27

intraflagellar transport 27

protein-coding

Homo sapiens

基因描述

Type Description
Definition intraflagellar transport 27

研究结论

Date Results Publications
2019-05-25 10:46:00 Loss of function IFT27 is associated with lethal fetal ciliopathy with renal agenesis. 29704304
2015-01-17 10:43:00 Study coupled human genetics with functional validation in zebrafish and identified IFT27 as a novel BBS gene (BBS19). 24488770

名称对应

Type IDs
Synonymous BBS19, RABL4, RAYL
Gene
UniProtKB-ID: IFT27_HUMAN
UniprotKB: Q9BW83
UniParc: UPI0000161F8B, UPI000013314C
EMBL: Z80897, CR456558, BC000566, AL022729, BT006815
Ensembl: ENSG00000100360
KO: hsa:11020
Nucleutide sequences
EMBL-CDS: AAH00566.1, CAA18787.1, CAG30444.1, AAP35461.1
Ensembl_TRS: ENST00000433985, ENST00000340630
Protein sequencees
Ensembl_PRO: ENSP00000393541, ENSP00000343593
RefSeq: NP_001349932.1, NP_006851.1, NP_001171172.1, XP_016884029.1
Others
UniRef100: UniRef100_Q9BW83
UniRef90: UniRef90_Q9BW83
UniRef50: UniRef50_Q9BW83
UniGene: Hs.415172
CCDS: CCDS13932.1, CCDS54523.1

全选

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