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MTND4P12 MT-ND4 pseudogene 12 [ Homo sapiens (human) ]

Gene ID: 100293090, updated on 10-Oct-2023

Summary

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Official Symbol
MTND4P12provided by HGNC
Official Full Name
MT-ND4 pseudogene 12provided by HGNC
Primary source
HGNC:HGNC:42199
See related
Ensembl:ENSG00000247627 AllianceGenome:HGNC:42199
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:
5q31.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (134926661..134928036, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (135453624..135454999, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (134262351..134263726, complement)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene pterin-4 alpha-carbinolamine dehydratase 2 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr5:134260709-134261470 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr5:134262317-134262960 Neighboring gene MT-ND5 pseudogene 11 Neighboring gene MT-ND6 pseudogene 4 Neighboring gene MT-ND4L pseudogene 30 Neighboring gene MT-ND3 pseudogene 25 Neighboring gene cation channel sperm associated 3 Neighboring gene NANOG hESC enhancer GRCh37_chr5:134312555-134313067 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr5:134325851-134326415

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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Markers

Other Names

  • mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 pseudogene 12

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_029205.1 

    Range
    101..1476
    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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    134926661..134928036 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    135453624..135454999 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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