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MTND4P19 MT-ND4 pseudogene 19 [ Homo sapiens (human) ]

Gene ID: 100873351, updated on 10-Oct-2023

Summary

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Official Symbol
MTND4P19provided by HGNC
Official Full Name
MT-ND4 pseudogene 19provided by HGNC
Primary source
HGNC:HGNC:42206
See related
AllianceGenome:HGNC:42206
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:
10q23.33
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (94763426..94774628, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (95642552..95653754, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (96523183..96534385, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene CTBP2 pseudogene 2 Neighboring gene cytochrome P450 family 2 subfamily C member 18 Neighboring gene Sharpr-MPRA regulatory region 9306 Neighboring gene CYP2C19 promoter Neighboring gene cytochrome P450 family 2 subfamily C member 19 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:96590143-96590741 Neighboring gene cytochrome P450 family 2 subfamily C member 58, pseudogene Neighboring gene ribosomal protein L7a pseudogene 52

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 4 pseudogene 19

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_032466.1 

    Range
    101..11303
    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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    94763426..94774628 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    95642552..95653754 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Other Literature Sources
Molecular Biology Databases