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