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57578 UNC79

57578

UNC79

unc-79 homolog, NALCN channel complex subunit

protein-coding

Homo sapiens

基因描述

Type Description
Definition unc-79 homolog, NALCN channel complex subunit

研究结论

Date Results Publications
2018-09-29 11:59:00 UNC79 variant is associated with neurodevelopmental diseases. 30167850
2016-05-14 11:08:00 UNC80 encodes a large protein that is necessary for the stability and function of NALCN and for bridging NALCN to UNC79 to form a functional complex 26708753
2010-06-30 22:05:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614
2010-06-14 12:11:00 In the Australian GWAS, one SNP achieved genomewide significance for comorbid AD/ND, rs12882384 in KIAA1409 on chromosome 14 (p = 4.86 x 10(-8))). 20158304

名称对应

Type IDs
Synonymous KIAA1409
Gene
UniProtKB-ID: UNC79_HUMAN
UniprotKB: Q9P2D8
UniParc: UPI00021CF3DB, UPI0000D62441, UPI00021CF3DC
EMBL: AL136338, AB037830, AL122023, AK125327, AL157858
Ensembl: ENSG00000133958, ENSG00000276416
KO: hsa:57578
Nucleutide sequences
EMBL-CDS: BAA92647.2, BAC86131.1
Ensembl_TRS: ENST00000393151, ENST00000629588, ENST00000621021, ENST00000627404, ENST00000553484, ENST00000615108, ENST00000256339, ENST00000627695
Protein sequencees
Ensembl_PRO: ENSP00000486167, ENSP00000479521, ENSP00000451360, ENSP00000256339, ENSP00000487436, ENSP00000376858, ENSP00000480937, ENSP00000485969
RefSeq: XP_016877007.1, XP_016877009.1, XP_011535325.1, NP_065869.3, XP_011535327.1, XP_016877002.1, XP_016877004.1, XP_016876995.1, XP_016876997.1, XP_016876998.1, XP_011535323.1, XP_024305435.1, XP_016876996.1, XP_011535330.1, XP_011535326.1, XP_011535320.1, XP_011535331.1, XP_024305436.1, XP_016877003.1, XP_011535322.1, XP_016877005.1, XP_016877006.1, XP_016876999.1, XP_016877008.1, NP_001333147.1, XP_011535329.1, XP_011535324.1, XP_011535328.1
Others
UniRef100: UniRef100_Q9P2D8
UniRef90: UniRef90_Q9P2D8
UniRef50: UniRef50_Q9P2D8
UniGene: Hs.126561
CCDS: CCDS9911.2

全选

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