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MEIS3P2 Meis homeobox 3 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 257468, updated on 25-Jan-2022

Summary

Official Symbol
MEIS3P2provided by HGNC
Official Full Name
Meis homeobox 3 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:17638
See related
AllianceGenome:HGNC:17638
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in several processes, including animal organ development; embryonic pattern specification; and positive regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Nov 2021]
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Genomic context

See MEIS3P2 in Genome Data Viewer
Location:
17p11.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 17 NC_000017.11 (20588850..20590815)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (20492163..20494128)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene CMT1A duplicated region transcript 15 like 2 Neighboring gene zinc finger SWIM-type containing 5 pseudogene 2 Neighboring gene differentially expressed in FDCP 8 homolog (mouse) pseudogene Neighboring gene long intergenic non-protein coding RNA 2088 Neighboring gene ribosomal protein S6 kinase B1 pseudogene Neighboring gene uncharacterized LOC105371583 Neighboring gene cytospin B pseudogene

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • Meis1 homolog 3 pseudogene 2
  • putative homeobox protein Meis3-like 2

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_002418.8 

    Range
    101..2066
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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
    20588850..20590815
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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