MEOX1

Source: Wikipedia, the free encyclopedia.
MEOX1
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
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[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Homeobox protein MOX-1 is a protein that in humans is encoded by the MEOX1 gene.[5][6]

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.[6]

Interactions

MEOX1 has been shown to

interact with PAX1[7] and PAX3.[7]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000005102 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000001493 - Ensembl, 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. PMID 7987315
    .
  6. ^ a b "Entrez Gene: MEOX1 mesenchyme homeobox 1".
  7. ^
    S2CID 40668112
    .

Further reading


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