Type | Description |
---|---|
Definition | ceruloplasmin |
Date | Results | Publications |
---|---|---|
2020-06-06 11:49:00 | This study concluded that even when the ferroportin expression is high, ceruloplasmin remains a limiting factor in the release of iron to the extracellular environment. | 31011744 |
2019-05-04 11:12:00 | HEPH and CP are not essential for intestinal iron absorption but are required for proper systemic iron distribution. | 30182051 |
2019-04-06 10:07:00 | results suggest that ablation of hephaestin and ceruloplasmin could lead to severe systemic iron deficiency and local tissue iron overload, which disrupt the whole body iron homeostasis and impact on tissue functions | 30060949 |
2019-03-09 12:46:00 | Ceruloplasmin regulates reelin processing, cofilin phosphorylation and neuronal organization in the developing brain. | 30077770 |
2019-01-12 11:27:00 | Results show that both HEPH and CP are expressed in subcutaneous adipose tissue. Ablation of either MCF leads to a compensatory increase in the other, which contributes to the balance of iron status. However, ablation of both induces severe iron deposition in adipocytes and displays disordered carbohydrate metabolism characterized as type 2 diabetes. | 29355933 |
Type | IDs |
---|---|
Synonymous | D3Ertd555e |
Gene |
UniProtKB-ID:
CERU_MOUSE,
G3X9T8_MOUSE,
E9PZD8_MOUSE,
Q8BU82_MOUSE,
G3X8Q5_MOUSE
UniprotKB:
Q61147,
G3X9T8,
E9PZD8,
Q8BU82,
G3X8Q5
UniParc:
UPI000024D8E7,
UPI00001F05E5,
UPI00000EAA8A,
UPI0000225E55,
UPI00005659F3
EMBL:
BC062957,
AC079442,
AK086999,
U49430
Ensembl:
ENSMUSG00000003617
KO:
mmu:12870
|
Nucleutide sequences |
EMBL-CDS:
AAB07996.1,
AAH62957.1,
BAC39781.1
Ensembl_TRS:
ENSMUST00000091309,
ENSMUST00000108325,
ENSMUST00000108329,
ENSMUST00000003714,
ENSMUST00000108328
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000088857,
ENSMUSP00000103961,
ENSMUSP00000103965,
ENSMUSP00000003714,
ENSMUSP00000103964
RefSeq:
NP_001263179.1,
NP_001361606.1,
NP_001263177.1,
XP_011247957.1,
NP_031778.2,
XP_006535444.1
|
Others |
UniRef100:
UniRef100_G3X8Q5,
UniRef100_E9PZD8,
UniRef100_G3X9T8,
UniRef100_Q61147
UniRef90:
UniRef90_P13635,
UniRef90_Q61147
UniRef50:
UniRef50_P13635
UniGene:
Mm.13787
CCDS:
CCDS38401.1
|
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