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MTND6P7 MT-ND6 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 106478945, updated on 10-Oct-2023

Summary

Official Symbol
MTND6P7provided by HGNC
Official Full Name
MT-ND6 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:39470
See related
Ensembl:ENSG00000224695 AllianceGenome:HGNC:39470
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

Location:
2p12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (82817538..82818061, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (82817740..82818263, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (83044662..83045185, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene MT-ND4 pseudogene 25 Neighboring gene MT-ND5 pseudogene 27 Neighboring gene MT-CYB pseudogene 7 Neighboring gene uncharacterized LOC105374831

Genomic regions, transcripts, and products

General gene information

Other Names

  • MTND6 pseudogene 7
  • mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 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_043693.1 

    Range
    101..624
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    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    82817538..82818061 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    82817740..82818263 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)