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MTND2P14 MT-ND2 pseudogene 14 [ Homo sapiens (human) ]

Gene ID: 100873223, updated on 10-Oct-2023

Summary

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Official Symbol
MTND2P14provided by HGNC
Official Full Name
MT-ND2 pseudogene 14provided by HGNC
Primary source
HGNC:HGNC:42115
See related
Ensembl:ENSG00000240796 AllianceGenome:HGNC:42115
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

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Location:
3q13.12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (106902173..106902523)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (109622069..109622419)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (106621020..106621370)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene nuclear-encoded mitochondrial tRNA-Gln (TTG) 4-1 Neighboring gene MT-CO1 pseudogene 35 Neighboring gene MT-ND1 pseudogene 16 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:106626782-106627464 Neighboring gene uncharacterized LOC107986021 Neighboring gene Sharpr-MPRA regulatory region 705 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:106641631-106642185 Neighboring gene RNA, U6 small nuclear 1308, pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 pseudogene 14

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_032426.1 

    Range
    101..451
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    106902173..106902523
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    109622069..109622419
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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