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17701 Msx1

17701

Msx1

msh homeobox 1

protein-coding

Mus musculus

基因描述

Type Description
Definition msh homeobox 1

研究结论

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

名称对应

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

全选

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研究热度

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