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MTND2P7 MT-ND2 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 100873179, updated on 10-Oct-2023

Summary

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Official Symbol
MTND2P7provided by HGNC
Official Full Name
MT-ND2 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:42141
See related
Ensembl:ENSG00000253970 AllianceGenome:HGNC:42141
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 MTND2P7 in Genome Data Viewer
Location:
8q24.22
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (133754739..133755449)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (134878757..134879467)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (134766982..134767692)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA SNORA40 Neighboring gene long intergenic non-protein coding RNA 3024 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28007 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:134708677-134709178 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr8:134770744-134771389 Neighboring gene MT-CO1 pseudogene 49 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr8:134781362-134781982 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:134783441-134783941 Neighboring gene uncharacterized LOC101927798

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 7

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_032446.1 

    Range
    101..811
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    133754739..133755449
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    134878757..134879467
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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