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MEP1AP2 meprin A subunit alpha pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 644777, updated on 12-Sep-2024

Summary

Official Symbol
MEP1AP2provided by HGNC
Official Full Name
meprin A subunit alpha pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:7017
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MEP1AL2
Annotation information
Note: GeneID:64477 (MEP1AP2) was annotated on the CHM1-1.1 alternate assembly, but is not found on the GRCh38 reference assembly. Experimental data in PMID:10405340 indicates the presence of multiple related sequences in this family on chromosome 9. [17 Jun 2014]
not in current annotation release
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Genomic context

See MEP1AP2 in Genome Data Viewer
Location:
9q21.11
Annotation release Status Assembly Chr Location
RS_2024_09 latest, but not current GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (70727366..70734147, complement)

General gene information

Other Names

  • meprin A, alpha (PABA peptide hydrolase) pseudogene
  • meprin A, alpha pseudogene 2
  • meprin A, alpha-like 2 (pseudogene)

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_083991.1 

    Range
    101..6882
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_006473.4: Suppressed sequence

    Description
    NG_006473.4: This RefSeq has been removed because it does not align to the current genome assembly.