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3798 KIF5A

3798

KIF5A

kinesin family member 5A

protein-coding

Homo sapiens

基因描述

Type Description
Definition kinesin family member 5A

研究结论

Date Results Publications
2020-08-22 15:25:00 Whole-exome sequencing identified novel KIF5A mutations in Chinese patients with amyotrophic lateral sclerosis and Charcot-Marie-Tooth type 2. 31422367
2019-12-28 12:34:00 KIF5A expression level was higher in the bladder cancer tissues than in the adjacent nontumor tissues. Patients with higher KIF5A expression displayed advanced clinical features and shorter survival time than those with lower KIF5A expression. 31354888
2019-12-21 12:01:00 it is an uncommon genetic determinant of ALS in Chinese patients. 30301576
2019-12-07 10:28:00 KIF5A mutation accounted for 0.41% (4/960) of Chinese patients with amyotrophic lateral sclerosis (ALS), which suggests that KIF5A is an uncommon cause of ALS in the Chinese population. 29954873
2019-08-10 11:11:00 KIF5A p.Ala361Val cause spastic paraplegia and primary progressive multiple sclerosis. 29908077

名称对应

Type IDs
Synonymous ALS25, D12S1889, MY050, NEIMY, NKHC, SPG10
Gene
UniProtKB-ID: KIF5A_HUMAN
UniprotKB: Q12840
UniParc: UPI000013DE4C
EMBL: BC146670, CH471054, AB210045, BC150208, U06698
Ensembl: ENSG00000155980
KO: hsa:3798
Nucleutide sequences
EMBL-CDS: BAE06127.1, AAI46671.1, EAW97030.1, AAA20231.1, AAI50209.1
Ensembl_TRS: ENST00000455537
Protein sequencees
Ensembl_PRO: ENSP00000408979
RefSeq: NP_004975.2, NP_001341634.1
Others
UniRef100: UniRef100_Q12840
UniRef90: UniRef90_Q12840
UniRef50: UniRef50_Q12840
UniGene: Hs.151219
CCDS: CCDS8945.1

全选

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研究热度

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