MSX1

Name

msh homeobox 1

Type

protein-coding

Position

4,859,665–4,863,936 (+)

Aliases

ECTD3, HOX7, HYD1, STHAG1

Ensembl

ENSG00000163132

RefSeq RNA

NM_002448.3

RefSeq protein

NP_002439.2

This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq, Jul 2008].

via MyGene.info

Gene · Ensembl

msh homeobox 1

Symbol

MSX1

Biotype

Protein coding

Organism

Homo sapiens

Location

4:4,859,665-4,863,936

Strand

Forward (+)

Assembly

GRCh38

Wikidata facts

Instance of

gene

Image

Protein MSX1 PDB 1ig7.png

via Wikidata · CC0