Type | Description |
---|---|
Definition | sorting nexin 19 |
Date | Results | Publications |
---|---|---|
2021-04-17 13:11:00 | Schizophrenia risk variants influence multiple classes of transcripts of sorting nexin 19 (SNX19). | 30635639 |
2010-04-07 21:40:00 | Observational study of gene-disease association. (HuGE Navigator) | 19752551 |
2009-12-02 21:41:00 | Observational study of gene-disease association. (HuGE Navigator) | 19730683 |
2009-03-25 21:36:00 | Observational study of gene-disease association. (HuGE Navigator) | 19023099 |
2008-12-03 21:30:00 | Observational study of gene-disease association. (HuGE Navigator) | 17975119 |
Type | IDs |
---|---|
Synonymous | CHET8 |
Gene |
UniProtKB-ID:
SNX19_HUMAN,
E9PJV7_HUMAN,
B7ZAU9_HUMAN,
E9PLV3_HUMAN
UniprotKB:
Q92543,
E9PJV7,
B7ZAU9,
E9PLV3
UniParc:
UPI000013D6A5,
UPI0001F77C33,
UPI0001F77C32,
UPI0001F77C31,
UPI000191548A
EMBL:
D87443,
AP001093,
BC031620,
AF395843,
AP000824,
AK316414
Ensembl:
ENSG00000120451
KO:
hsa:399979
|
Nucleutide sequences |
EMBL-CDS:
AAK73124.1,
BAA13384.2,
AAH31620.1,
BAH14785.1
Ensembl_TRS:
ENST00000533214,
ENST00000265909,
ENST00000534726,
ENST00000528555,
ENST00000530356
|
Protein sequencees |
Ensembl_PRO:
ENSP00000435390,
ENSP00000265909,
ENSP00000433699,
ENSP00000432307,
ENSP00000435122
RefSeq:
NP_001334854.1,
NP_001288018.1,
XP_011541127.1,
NP_001334853.1,
XP_011541123.1,
NP_001334849.2,
NP_001334852.2,
NP_001334851.2,
XP_011541122.1,
NP_001334856.1,
XP_011541128.1,
NP_001334850.2,
NP_001334848.2,
NP_055573.3,
XP_024304289.1,
NP_001334847.2,
XP_011541126.1,
NP_001334855.1
|
Others |
UniRef100:
UniRef100_Q92543,
UniRef100_B7ZAU9
UniRef90:
UniRef90_Q92543,
UniRef90_B7ZAU9
UniRef50:
UniRef50_A0A384BVF4,
UniRef50_Q92543
UniGene:
Hs.444024
CCDS:
CCDS86261.1,
CCDS31721.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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