MSX1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 4[12]
- Cytogenetic location
- 4p16.2[15]
- Encodes
- Msh homeobox 1[10]
- Expressed in
- buccal mucosa cell, Epithelium of choroid plexus, canal of the cervix, periodontal fiber, saphenous vein, endometrium, oocyte, vena cava, secondary oocyte, urethra[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- tooth and nail syndrome[13]
- HomoloGene ID
- 1836[3]
- Strand orientation
- forward strand[14]
🏷️ Also known as
en ECTD3
en HOX7
en HYD1
en msh homeobox 1
en MSX1
en STHAG1
🔖 Identifiers · 11
- Image (Wikimedia Commons)
- Protein MSX1 PDB 1ig7.png ↗
- Ensembl gene ID
- ENSG00000163132
- Ensembl transcript ID
- ENST00000468421, ENST00000382723
- Entrez Gene ID
- 4487
- Exact match
- identifiers.org
- Freebase ID
- /m/03cwn8y
- HGNC ID
- 7391
- HGNC gene symbol
- MSX1
- OMIM ID
- 142983
- RefSeq RNA ID
- NM_002448
- UMLS CUI
- C1417387
🔗 Connections
Expressed in 6
← Genetic association 2
Chromosome 1
Found in taxon 1
Instance of 1
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