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MTND2P39 MT-ND2 pseudogene 39 [ Homo sapiens (human) ]

Gene ID: 107075312, updated on 13-May-2022

Summary

Official Symbol
MTND2P39provided by HGNC
Official Full Name
MT-ND2 pseudogene 39provided by HGNC
Primary source
HGNC:HGNC:52070
See related
Ensembl:ENSG00000230130 AllianceGenome:HGNC:52070
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See MTND2P39 in Genome Data Viewer
Location:
Xq27.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (143434517..143435280)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (141743799..141744562)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (142522311..142523074)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene piggyBac transposable element derived 4 pseudogene 6 Neighboring gene MT-ND1 pseudogene 33 Neighboring gene SPANX family member N3 Neighboring gene MYCL pseudogene 3

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 39

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_046513.1 

    Range
    101..864
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    143434517..143435280
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    141743799..141744562
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)