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MEOX1 mesenchyme homeobox 1 [ Homo sapiens (human) ]

Gene ID: 4222, updated on 7-Jun-2020

Summary

Official Symbol
MEOX1provided by HGNC
Official Full Name
mesenchyme homeobox 1provided by HGNC
Primary source
HGNC:HGNC:7013
See related
Ensembl:ENSG00000005102 MIM:600147
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
KFS2; MOX1
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 molecular signaling network regulating somite development. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Expression
Biased expression in fat (RPKM 15.6), heart (RPKM 8.2) and 11 other tissues See more
Orthologs

Genomic context

See MEOX1 in Genome Data Viewer
Location:
17q21.31
Exon count:
4
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (43640389..43661977, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (41717757..41739262, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein L29 pseudogene 31 Neighboring gene DEAH-box helicase 8 Neighboring gene ETS variant transcription factor 4 Neighboring gene uncharacterized LOC107985085 Neighboring gene long intergenic non-protein coding RNA 2594 Neighboring gene Wolf-Hirschhorn syndrome candidate 1-like 2, pseudogene

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

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
DNA-binding transcription activator activity, RNA polymerase II-specific IEA
Inferred from Electronic Annotation
more info
 
DNA-binding transcription factor activity ISS
Inferred from Sequence or Structural Similarity
more info
 
DNA-binding transcription factor activity, RNA polymerase II-specific ISA
Inferred from Sequence Alignment
more info
 
DNA-binding transcription factor activity, RNA polymerase II-specific ISM
Inferred from Sequence Model
more info
PubMed 
HMG box domain binding IEA
Inferred from Electronic Annotation
more info
 
RNA polymerase II proximal promoter sequence-specific DNA binding IEA
Inferred from Electronic Annotation
more info
 
chromatin binding IEA
Inferred from Electronic Annotation
more info
 
molecular_function ND
No biological Data available
more info
 
protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
sequence-specific DNA binding ISS
Inferred from Sequence or Structural Similarity
more info
 
Process Evidence Code Pubs
biological_process ND
No biological Data available
more info
 
hematopoietic stem cell differentiation ISS
Inferred from Sequence or Structural Similarity
more info
 
multicellular organism development TAS
Traceable Author Statement
more info
PubMed 
positive regulation of transcription by RNA polymerase II IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
sclerotome development ISS
Inferred from Sequence or Structural Similarity
more info
 
somite development IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
somite development ISS
Inferred from Sequence or Structural Similarity
more info
 
somite specification IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
cytoplasm ISS
Inferred from Sequence or Structural Similarity
more info
 
nuclear chromatin ISA
Inferred from Sequence Alignment
more info
 
nucleus IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
nucleus ISS
Inferred from Sequence or Structural Similarity
more info
 

NCBI Reference Sequences (RefSeq)

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_032987.1 RefSeqGene

    Range
    4973..26506
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001040002.2NP_001035091.1  homeobox protein MOX-1 isoform 3

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) differs in the 5' UTR and coding region (compared to variant 1), resulting in a protein that maintains the reading frame but is shorter at the N- terminus, compared to isoform 1.
    Source sequence(s)
    AC004149, AW410297, BE898972, BQ003431, BQ028272, BX284090, U10492
    Consensus CDS
    CCDS42343.1
    UniProtKB/Swiss-Prot
    P50221
    Related
    ENSP00000377271.2, ENST00000393661.2
    Conserved Domains (1) summary
    pfam00046
    Location:60112
    Homeobox; Homeobox domain
  2. NM_004527.4NP_004518.1  homeobox protein MOX-1 isoform 1

    See identical proteins and their annotated locations for NP_004518.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant represents the longest transcript and encodes the longest isoform (1).
    Source sequence(s)
    AC004149, BG677020, BQ028272, U10492
    Consensus CDS
    CCDS11466.1
    UniProtKB/Swiss-Prot
    P50221
    Related
    ENSP00000321684.4, ENST00000318579.9
    Conserved Domains (1) summary
    pfam00046
    Location:175227
    Homeobox; Homeobox domain
  3. NM_013999.3NP_054705.1  homeobox protein MOX-1 isoform 2

    See identical proteins and their annotated locations for NP_054705.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) lacks an exon in the coding region that results in a frameshift and a premature stop codon compared to variant 1. The encoded isoform (2) is shorter and has a distinct C-terminus compared to isoform 1.
    Source sequence(s)
    BG677020, BQ028272, U10493
    Consensus CDS
    CCDS11467.1
    UniProtKB/Swiss-Prot
    P50221
    Related
    ENSP00000449049.2, ENST00000549132.2

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p13 Primary Assembly

    Range
    43640389..43661977 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_011524818.2XP_011523120.1  homeobox protein MOX-1 isoform X1

    Conserved Domains (1) summary
    pfam00046
    Location:175216
    Homeobox; Homeobox domain
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