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中文人类
MSX1 - Msh Homeobox 1
Alias:
HOX7
HYD1
ECTD3
STHAG1
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这个基因编码肌肉片段同源盒基因家族的成员。编码的蛋白质在胚胎发育过程中作为转录抑制因子，通过与核心转录复合物组件和其他同源蛋白相互作用发挥作用。它还可能参与肢斑模式的形成，颅面发育，尤其是牙发生，以及肿瘤生长的抑制。这个基因的突变（曾被称为同源盒7）与非综合征性唇裂（伴有或不伴有腭裂）5、Witkop综合征、Wolf-Hirschhorn综合征和常染色体显性牙列缺失有关。[RefSeq,2008年7月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
MSX1 Genetics information (+)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
Mutations
Transcripts & Proteins
Table View
Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
Organ
Abundance
Alphabetical
Cell-specific RNA expression
Organ
Abundance
Alphabetical
Interactions
Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
Related Mouse Models
Type
Name
MGI
Strain of Origin
Publications
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Link
References Literature
Title
PMID
Journal
Year
IF
