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MEIS3P1 Meis homeobox 3 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 4213, updated on 1-Aug-2020

Summary

Official Symbol
MEIS3P1provided by HGNC
Official Full Name
Meis homeobox 3 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:7002
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MRG2; MEIS3; MEIS4
Summary
This gene appears to be a retrotransposed pseudogene based on its lack of exons compared to other family members, one of which is found on chromosome 19 (MEIS3). It does appear to be transcribed and has an ORF that may encode a protein of similar size and sequence to that encoded by MEIS3. [provided by RefSeq, Jul 2008]

Genomic context

See MEIS3P1 in Genome Data Viewer
Location:
17p12
Exon count:
1
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (15786850..15789705)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (15690164..15693019)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene zinc finger SWIM-type containing 5 pseudogene 1 Neighboring gene RNA, 5S ribosomal pseudogene 436 Neighboring gene interleukin 6 signal transducer pseudogene 1 Neighboring gene long intergenic non-protein coding RNA 2087 Neighboring gene uncharacterized LOC105371557 Neighboring gene SPECC1 pseudogene 1

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • CTD-3157E16.2
  • Homeobox protein Meis3
  • Meis homolog 3
  • Meis1 homolog 3 pseudogene 1
  • Meis1, myeloid ecotropic viral integration site 1 homolog 3
  • Meis1, myeloid ecotropic viral integration site 1 homolog 4
  • Putative homeobox protein Meis3-like 1

Gene Ontology Provided by GOA

Function Evidence Code Pubs
DNA binding IEA
Inferred from Electronic Annotation
more info
 
DNA-binding transcription activator activity, RNA polymerase II-specific IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Process Evidence Code Pubs
animal organ morphogenesis IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
brain development IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
embryonic pattern specification IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
eye development IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
positive regulation of cell proliferation IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
positive regulation of transcription by RNA polymerase II IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Component Evidence Code Pubs
nucleus IEA
Inferred from Electronic Annotation
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.

RNA

  1. NR_002211.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC015922, AK054814, BM463727, BQ575773, BU685266, U68385

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20200522

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
    15786850..15789705
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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