Type | Description |
---|---|
Definition | solute carrier family 39 (metal ion transporter), member 13 |
Date | Results | Publications |
---|---|---|
2020-10-31 13:16:00 | Loss of the dermis zinc transporter ZIP13 promotes the mildness of fibrosarcoma by inhibiting autophagy. | 31636298 |
2020-01-18 12:08:00 | we have clarified the functional differences between ZIP7 and ZIP13 and show that their different regulation of cellular zinc homeostasis is critical for dermal development and homeostasis. | 31412620 |
2017-09-16 10:56:00 | Both gain- and loss-of-function studies showed that an accumulation of the CCAAT/enhancer binding protein-beta (C/EBP-beta) protein, which cooperates with dominant transcriptional co-regulator PR domain containing 16 (PRDM16) to determine brown/beige adipocyte lineage, is essential for the enhanced adipocyte browning caused by the loss of ZIP13 | 28854265 |
2016-10-01 11:58:00 | This study concluded that skin fragility due to defective ZIP13 protein may be attributable to impaired extracellular matrix synthesis accompanied by abnormal peripheral TGF-beta homeostasis. | 26050750 |
2010-01-21 00:00:00 | The Slc39a13-KO mouse represents a novel animal model linking zinc metabolism, BMP/TGF-beta signaling and connective tissue dysfunction. | 18985159 |
Type | IDs |
---|---|
Synonymous | 1100001L14Rik, AA387663, ZIP-13, ZIP13 |
Gene |
UniProtKB-ID:
S39AD_MOUSE,
B2RQ45_MOUSE
UniprotKB:
Q8BZH0,
B2RQ45
UniParc:
UPI00000EA414,
UPI0000021127,
UPI0000574FDA
EMBL:
BC100463,
AL691439,
BC020106,
AK035296,
AK003191,
BC125525,
BC137752,
AK156951
Ensembl:
ENSMUSG00000002105
KO:
mmu:68427
|
Nucleutide sequences |
EMBL-CDS:
AAH20106.1,
AAI00464.1,
BAC29020.1,
BAE33911.1,
BAB22631.1,
AAI25526.1,
AAI37753.1
Ensembl_TRS:
ENSMUST00000073575,
ENSMUST00000079976,
ENSMUST00000111436
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000073263,
ENSMUSP00000107063,
ENSMUSP00000078892
RefSeq:
XP_006500162.1,
XP_036018417.1,
XP_006500163.1,
NP_080997.1,
XP_030107890.1,
NP_001277694.1,
XP_017174725.1,
XP_030107891.1,
XP_030107889.1,
XP_006500164.1
|
Others |
UniRef100:
UniRef100_Q8BZH0
UniRef90:
UniRef90_Q8BZH0
UniRef50:
UniRef50_Q96H72
UniGene:
Mm.192375
CCDS:
CCDS71095.1,
CCDS16424.1
|
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