Type | Description |
---|---|
Definition | msh homeobox 1 |
Date | Results | Publications |
---|---|---|
2021-02-06 13:50:00 | Phosphorylation of Msx1 promotes cell proliferation through the Fgf9/18-MAPK signaling pathway during embryonic limb development. | 33080014 |
2020-12-26 13:12:00 | Msx1 deficiency interacts with hypoxia and induces a morphogenetic regulation during mouse lip development. | 32467233 |
2020-11-28 13:11:00 | The C-terminal region including the MH6 domain of Msx1 regulates skeletal development. | 32192766 |
2020-09-19 16:22:00 | Msx1 loss suppresses formation of the ectopic crypts developed in the Apc-deficient small intestinal epithelium. | 30733598 |
2020-07-18 12:14:00 | Loss of Msx1 and Msx2 in neural stem cells lead the small size of the brain in mice. | 31221479 |
Type | IDs |
---|---|
Synonymous | AA675338, AI324650, Hox-7, Hox7, Hox7.1, msh |
Gene |
UniProtKB-ID:
MSX1_MOUSE
UniprotKB:
P13297
UniParc:
UPI00000254D5
EMBL:
BC016426,
X14457,
X14759,
M38575,
X59251,
AF308572,
AC114671,
CH466524
Ensembl:
ENSMUSG00000048450
KO:
mmu:17701
|
Nucleutide sequences |
EMBL-CDS:
CAA32871.1,
AAG32466.1,
EDL37531.1,
CAA32626.1,
AAA37823.1,
CAA41944.1,
AAH16426.1
Ensembl_TRS:
ENSMUST00000063116
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000058354
RefSeq:
NP_034965.2
|
Others |
UniRef100:
UniRef100_P13297
UniRef90:
UniRef90_P13297
UniRef50:
UniRef50_P13297
UniGene:
Mm.256509
CCDS:
CCDS19249.1
|
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Refseq |
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