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79858 NEK11

79858

NEK11

NIMA related kinase 11

protein-coding

Homo sapiens

基因描述

Type Description
Definition NIMA related kinase 11

研究结论

Date Results Publications
2021-02-27 13:44:00 NEK11 as a candidate high-penetrance melanoma susceptibility gene. 31704778
2020-11-21 13:31:00 Exome sequencing revealed DNA variants in NCOR1, IGF2BP1, SGLT2 and NEK11 as potential novel causes of ketotic hypoglycemia in children. 32034166
2016-06-11 11:36:00 contributes to response of colorectal cancer cells to genotoxic agents and is essential for survival either with or without exposure to DNA damage 26501353
2015-02-28 12:51:00 Results show that downregulation of NEK11 in drug resistant cells might contribute to drug resistance in ovarian cancer. 24969318
2010-06-30 22:06:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614

名称对应

Type IDs
Gene
UniProtKB-ID: NEK11_HUMAN, E9PHI8_HUMAN, B4DDN2_HUMAN, B4DM56_HUMAN
UniprotKB: Q8NG66, E9PHI8, B4DDN2, B4DM56
UniParc: UPI0001AE7623, UPI000006D8DE, UPI00017A6D50, UPI00001408C9, UPI00017A7549, UPI000006D9F6, UPI000013F25D
EMBL: AC083908, AK297300, AK293261, CH471052, AC121332, AK027148, AC055733, BC028587, AB071996, AB071997, AL833472, AC010210, AC116424
Ensembl: ENSG00000114670
KO: hsa:79858
Nucleutide sequences
EMBL-CDS: AAH28587.1, BAC06350.1, BAB15672.1, EAW79213.1, BAC06351.1, CAI46114.1, BAG56793.1, BAG59768.1
Ensembl_TRS: ENST00000356918, ENST00000508196, ENST00000507910, ENST00000511262, ENST00000383366, ENST00000510688, ENST00000510769
Protein sequencees
Ensembl_PRO: ENSP00000426662, ENSP00000423458, ENSP00000421851, ENSP00000372857, ENSP00000425114, ENSP00000349389, ENSP00000421549
RefSeq: NP_001339961.1, NP_001339969.1, XP_016862717.1, NP_001339952.1, NP_001339965.1, NP_001339977.1, NP_001339956.1, NP_665917.1, XP_016862698.1, NP_001339963.1, XP_016862722.1, XP_024309528.1, NP_001339958.1, NP_001339974.1, XP_024309524.1, XP_011511477.1, NP_001339954.1, NP_001339970.1, NP_001308149.1, NP_001339957.1, NP_001139475.1, XP_024309526.1, NP_001339975.1, XP_024309523.1, NP_001339959.1, NP_001339953.1, XP_024309527.1, XP_016862697.1, NP_001339962.1, XP_016862711.1, NP_001308152.1, NP_001339966.1, NP_001339973.1, XP_016862699.1, NP_001339960.1, XP_016862709.1, XP_011511475.1, XP_016862710.1, NP_001339967.1, XP_016862696.1, XP_011511476.1, NP_001339955.1, XP_016862708.1, XP_016862695.1, NP_001339951.1, NP_001339968.1, NP_001308150.1, XP_024309525.1, NP_001339971.1, NP_001339972.1, NP_001308151.1, NP_001308153.1, NP_079076.3
Others
UniRef100: UniRef100_Q8NG66, UniRef100_B4DDN2, UniRef100_B4DM56, UniRef100_E9PHI8
UniRef90: UniRef90_Q8NG66, UniRef90_A0A2K6B9K4, UniRef90_B4DDN2
UniRef50: UniRef50_Q8NG66
UniGene: Hs.657336
CCDS: CCDS54639.1, CCDS3069.1, CCDS82836.1, CCDS46915.1

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