Type | Description |
---|---|
Definition | complement C4A (Rodgers blood group) |
Date | Results | Publications |
---|---|---|
2020-10-24 14:10:00 | Complement genes contribute sex-biased vulnerability in diverse disorders. | 32499649 |
2020-10-03 12:54:00 | Serum complement C4 is an important prognostic factor for IgA nephropathy: a retrospective study. | 31272400 |
2020-09-05 13:56:00 | Clinical significance of C4d deposition in renal tissues from patients with primary Sjogren's syndrome-a preliminary study. | 31138153 |
2020-02-29 11:30:00 | this study shows that elevated complement C4 levels are associated with postnatal pregnancy-related venous thrombosis | 31254974 |
2020-02-08 12:27:00 | serum component 4 level is lower in patients with schizophrenia than in the controls, and the results apply to both males and females. | 30933047 |
Type | IDs |
---|---|
Synonymous | C4, C4A2, C4A3, C4A4, C4A6, C4AD, C4S, CO4, CPAMD2, RG |
Gene |
UniProtKB-ID:
CO4A_HUMAN
UniprotKB:
P0C0L4
UniParc:
UPI00001AF648,
UPI0001574E5D
EMBL:
AY379960,
AY379925,
K00830,
CR936924,
AY379964,
AY379933,
BC146849,
AY379965,
AY379931,
M59816,
X77491,
BC171786,
L26261,
AY379932,
BC151204,
AY379929,
K02403,
AY379966,
BC012372,
U77886,
M59815,
AY379927,
AL844853,
AY379935,
BC144546,
AY379926,
AY379928,
AY379963,
M14824,
AL929593,
V00502,
AB209989,
AY379930,
AL645922,
AY379962,
BC063289,
AY379934,
BC146673
Ensembl:
ENSG00000244731,
ENSG00000206340,
ENSG00000227746
KO:
hsa:720,
hsa:721
|
Nucleutide sequences |
EMBL-CDS:
AAH12372.2,
CAA54627.1,
AAR89155.1,
AAR89164.1,
AAR89157.1,
AAA51855.1,
AAI46674.1,
AAR89152.1,
AAR89167.1,
AAR89166.1,
AAR89170.1,
AAR89158.1,
AAR89154.1,
AAI44547.1,
AAR89159.1,
AAI46850.1,
AAR89161.1,
AAH63289.1,
AAI51205.1,
AAR89169.1,
AAR89168.1,
AAA20121.2,
AAR89162.1,
AAA36229.1,
AAI71786.1,
CAA23760.1,
AAK49810.1,
AAA52292.1,
AAR89160.1,
AAR89153.1,
BAE06071.1,
AAB59537.1,
AAR89156.1
Ensembl_TRS:
ENST00000498271,
ENST00000428956,
ENST00000421274,
ENST00000383325
|
Protein sequencees |
Ensembl_PRO:
ENSP00000372815,
ENSP00000396688,
ENSP00000420212,
ENSP00000388662
RefSeq:
NP_001239133.1,
NP_009224.2
|
Others |
UniRef100:
UniRef100_P0C0L4
UniRef90:
UniRef90_P0C0L4
UniRef50:
UniRef50_P0C0L4
UniGene:
Hs.534847,
Hs.720022
CCDS:
CCDS59005.1,
CCDS47404.1
|
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Refseq |
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