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MEOX1

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Protein-coding gene in the species Homo sapiens
MEOX1
Identifiers
AliasesMEOX1, KFS2, MOX1, mesenchyme homeobox 1
External IDsOMIM: 600147; MGI: 103220; HomoloGene: 3326; GeneCards: MEOX1; OMA:MEOX1 - orthologs
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)
Chromosome 17 (human)Genomic location for MEOX1Genomic location for MEOX1
Band17q21.31Start43,640,389 bp
End43,661,922 bp
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)
Chromosome 11 (mouse)Genomic location for MEOX1Genomic location for MEOX1
Band11 D|11 65.48 cMStart101,768,336 bp
End101,785,200 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • tendon of biceps brachii

  • subcutaneous adipose tissue

  • apex of heart

  • Achilles tendon

  • parietal pleura

  • lactiferous duct

  • abdominal fat

  • synovial joint

  • synovial membrane

  • saphenous vein
Top expressed in
  • somite

  • semi-lunar valve

  • intermediate mesoderm

  • aortic valve

  • ankle joint

  • endocardial cushion

  • sclerotome

  • interventricular septum

  • urethra

  • primitive streak
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

4222

17285

Ensembl

ENSG00000005102

ENSMUSG00000001493

UniProt

P50221

P32442

RefSeq (mRNA)

NM_001040002
NM_004527
NM_013999

NM_010791

RefSeq (protein)

NP_001035091
NP_004518
NP_054705

NP_034921

Location (UCSC)Chr 17: 43.64 – 43.66 MbChr 11: 101.77 – 101.79 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Homeobox protein MOX-1 is a protein that in humans is encoded by the MEOX1 gene.

Function

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.

Interactions

MEOX1 has been shown to interact with PAX1 and PAX3.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000005102Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000001493Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Futreal PA, Cochran C, Rosenthal J, Miki Y, Swenson J, Hobbs M, Bennett LM, Haugen-Strano A, Marks J, Barrett JC (Jan 1995). "Isolation of a diverged homeobox gene, MOX1, from the BRCA1 region on 17q21 by solution hybrid capture". Hum Mol Genet. 3 (8): 1359–64. doi:10.1093/hmg/3.8.1359. PMID 7987315.
  6. ^ "Entrez Gene: MEOX1 mesenchyme homeobox 1".
  7. ^ Stamataki D, Kastrinaki M, Mankoo BS, Pachnis V, Karagogeos D (Jun 2001). "Homeodomain proteins Mox1 and Mox2 associate with Pax1 and Pax3 transcription factors". FEBS Lett. 499 (3): 274–8. doi:10.1016/S0014-5793(01)02556-X. PMID 11423130. S2CID 40668112.

Further reading

Transcription factors and intracellular receptors
(1) Basic domains
(1.1) Basic leucine zipper (bZIP)
(1.2) Basic helix-loop-helix (bHLH)
Group A
Group B
Group C
bHLH-PAS
Group D
Group E
Group F
bHLH-COE
(1.3) bHLH-ZIP
(1.4) NF-1
(1.5) RF-X
(1.6) Basic helix-span-helix (bHSH)
(2) Zinc finger DNA-binding domains
(2.1) Nuclear receptor (Cys4)
subfamily 1
subfamily 2
subfamily 3
subfamily 4
subfamily 5
subfamily 6
subfamily 0
(2.2) Other Cys4
(2.3) Cys2His2
(2.4) Cys6
(2.5) Alternating composition
(2.6) WRKY
(3) Helix-turn-helix domains
(3.1) Homeodomain
Antennapedia
ANTP class
protoHOX
Hox-like
metaHOX
NK-like
other
(3.2) Paired box
(3.3) Fork head / winged helix
(3.4) Heat shock factors
(3.5) Tryptophan clusters
(3.6) TEA domain
  • transcriptional enhancer factor
(4) β-Scaffold factors with minor groove contacts
(4.1) Rel homology region
(4.2) STAT
(4.3) p53-like
(4.4) MADS box
(4.6) TATA-binding proteins
(4.7) High-mobility group
(4.9) Grainyhead
(4.10) Cold-shock domain
(4.11) Runt
(0) Other transcription factors
(0.2) HMGI(Y)
(0.3) Pocket domain
(0.5) AP-2/EREBP-related factors
(0.6) Miscellaneous
see also transcription factor/coregulator deficiencies


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