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MEOX2 mesenchyme homeobox 2 [ Homo sapiens (human) ]

Gene ID: 4223, updated on 27-Nov-2024

Summary

Official Symbol
MEOX2provided by HGNC
Official Full Name
mesenchyme homeobox 2provided by HGNC
Primary source
HGNC:HGNC:7014
See related
Ensembl:ENSG00000106511 MIM:600535; AllianceGenome:HGNC:7014
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
GAX; MOX2
Summary
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 regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease. [provided by RefSeq, Jul 2008]
Expression
Biased expression in placenta (RPKM 25.8), fat (RPKM 23.2) and 13 other tissues See more
Orthologs
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Genomic context

See MEOX2 in Genome Data Viewer
Location:
7p21.2
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (15611212..15686683, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (15744456..15819945, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (15650837..15726308, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene alkylglycerol monooxygenase Neighboring gene uncharacterized LOC124901592 Neighboring gene Sharpr-MPRA regulatory region 14752 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:15557538-15558346 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr7:15586656-15587206 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr7:15587207-15587755 Neighboring gene uncharacterized LOC124901591 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:15638304-15638834 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:15638835-15639363 Neighboring gene uncharacterized LOC105375166 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:15724672-15725504 Neighboring gene long intergenic non-protein coding RNA 2587 Neighboring gene ribosomal protein L36a pseudogene 26

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in angiogenesis IEA
Inferred from Electronic Annotation
more info
 
involved_in limb development IEA
Inferred from Electronic Annotation
more info
 
involved_in negative regulation of cell migration involved in sprouting angiogenesis IGI
Inferred from Genetic Interaction
more info
PubMed 
involved_in positive regulation of transcription by RNA polymerase II IDA
Inferred from Direct Assay
more info
PubMed 
involved_in positive regulation of transcription by RNA polymerase II IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in regulation of transcription by RNA polymerase II IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in roof of mouth development IEA
Inferred from Electronic Annotation
more info
 
involved_in skeletal muscle tissue development IEA
Inferred from Electronic Annotation
more info
 
involved_in somite development IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in somite specification IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in chromatin ISA
Inferred from Sequence Alignment
more info
 
located_in cytoplasm IDA
Inferred from Direct Assay
more info
PubMed 
located_in nuclear speck IEA
Inferred from Electronic Annotation
more info
 
is_active_in nucleus IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in nucleus IDA
Inferred from Direct Assay
more info
PubMed 

General protein information

Preferred Names
homeobox protein MOX-2
Names
growth arrest-specific homeobox

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_032988.1 RefSeqGene

    Range
    5001..80472
    Download
    GenBank, FASTA, Sequence Viewer (Graphics), LRG_704

mRNA and Protein(s)

  1. NM_005924.5NP_005915.2  homeobox protein MOX-2

    See identical proteins and their annotated locations for NP_005915.2

    Status: REVIEWED

    Source sequence(s)
    BC017021, BQ025060, DA586635
    Consensus CDS
    CCDS34605.1
    UniProtKB/Swiss-Prot
    A4D127, B2R8I7, O75263, P50222, Q9UPL6
    UniProtKB/TrEMBL
    Q6FHY5
    Related
    ENSP00000262041.5, ENST00000262041.6
    Conserved Domains (2) summary
    COG5576
    Location:160284
    COG5576; Homeodomain-containing transcription factor [Transcription]
    pfam00046
    Location:191243
    Homeobox; Homeobox domain

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    15611212..15686683 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    15744456..15819945 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)