MEOX1
Sign in to saveAlso known as KFS2, MOX1, mesenchyme homeobox 1
Mesenchyme homeobox 1 (MEOX1) is a protein that in humans is encoded by the MEOX1 gene.
In the Vinony graph
Vinony's link graph records 813 inbound references to MEOX1, and connects out to PubMed, human chromosome 17 and homeobox.
It is catalogued under the topic Genes on human chromosome 17.
Vinony links it to 5 Wikipedia language editions.
Gene data
MEOX1- Name
- mesenchyme homeobox 1
- Type
- protein-coding
- Position
- 43,640,072–43,661,929 (−)
- Aliases
- KFS2, MOX1
- Ensembl
- ENSG00000005102
- RefSeq RNA
- NM_001040002.2, NM_001445822.1, NM_004527.4, NM_013999.4, XM_011524818.3
- RefSeq protein
- NP_001035091.1, NP_001432751.1, NP_004518.1, NP_054705.1, XP_011523120.1
This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the molecular signaling network regulating somite development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
mesenchyme homeobox 1
- Symbol
- MEOX1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 17:43,640,072-43,661,929
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 3326
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/4222
- genomic end
- 43661922
- genomic start
- 43640389
- chromosome
- human chromosome 17
- cytogenetic location
- 17q21.31
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Function
- Interactions
- References
- Further reading
Mesenchyme homeobox 1 (MEOX1) is a protein that in humans is encoded by the MEOX1 gene.
== Function ==
Excerpted from Wikipedia’s “MEOX1” article, available under the CC BY-SA 4.0 licence.