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MTND2P2 MT-ND2 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 56168, updated on 25-Jan-2022

Summary

Official Symbol
MTND2P2provided by HGNC
Official Full Name
MT-ND2 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:23767
See related
Ensembl:ENSG00000229954 AllianceGenome:HGNC:23767
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
bA522L3.2
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Genomic context

See MTND2P2 in Genome Data Viewer
Location:
Xq22.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (102786814..102788388)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (102041742..102043316)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ARMCX5-GPRASP2 readthrough Neighboring gene basic helix-loop-helix family member b9 Neighboring gene long intergenic non-protein coding RNA 630 Neighboring gene MT-ND1 pseudogene 32 Neighboring gene MT-CO1 pseudogene 19 Neighboring gene MT-CO2 pseudogene 19

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • MTND2 pseudogene 2
  • NADH dehydrogenase 2 pseudogene 2
  • mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 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_002320.3 

    Range
    101..1675
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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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    102786814..102788388
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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