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MTND2P26 MT-ND2 pseudogene 26 [ Homo sapiens (human) ]

Gene ID: 100873349, updated on 17-Sep-2024

Summary

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Official Symbol
MTND2P26provided by HGNC
Official Full Name
MT-ND2 pseudogene 26provided by HGNC
Primary source
HGNC:HGNC:42127
See related
Ensembl:ENSG00000254565 AllianceGenome:HGNC:42127
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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See MTND2P26 in Genome Data Viewer
Location:
11q22.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (103406219..103407241, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (103410115..103411137, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (103276947..103277969, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene dynein cytoplasmic 2 heavy chain 1 Neighboring gene MT-CO2 pseudogene 15 Neighboring gene MT-CO1 pseudogene 15 Neighboring gene MT-ND1 pseudogene 36 Neighboring gene NANOG hESC enhancer GRCh37_chr11:103452251-103453176 Neighboring gene NANOG hESC enhancer GRCh37_chr11:103454489-103455412 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr11:103496216-103497415 Neighboring gene uncharacterized LOC105369463 Neighboring gene eukaryotic translation initiation factor 4E binding protein 2 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 26

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_032438.1 

    Range
    101..1123
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    103406219..103407241 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    103410115..103411137 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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