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MTND1P21 MT-ND1 pseudogene 21 [ Homo sapiens (human) ]

Gene ID: 100873340, updated on 10-Oct-2023

Summary

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Official Symbol
MTND1P21provided by HGNC
Official Full Name
MT-ND1 pseudogene 21provided by HGNC
Primary source
HGNC:HGNC:42070
See related
Ensembl:ENSG00000235940 AllianceGenome:HGNC:42070
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:
10p12.31
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (20804281..20804580)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (20822828..20823127)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (21093210..21093509)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105376442 Neighboring gene H3K27ac hESC enhancer GRCh37_chr10:20885982-20886482 Neighboring gene microRNA 4675 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr10:21045700-21046232 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:21046233-21046763 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr10:21105746-21106945 Neighboring gene uncharacterized LOC102725112 Neighboring gene nebulette Neighboring gene Sharpr-MPRA regulatory region 670 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_11562 Neighboring gene uncharacterized LOC124902389

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 1 pseudogene 21

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_032404.1 

    Range
    101..400
    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
    20804281..20804580
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    20822828..20823127
    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