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MTND1P11 MT-ND1 pseudogene 11 [ Homo sapiens (human) ]

Gene ID: 100873212, updated on 10-Oct-2023

Summary

Official Symbol
MTND1P11provided by HGNC
Official Full Name
MT-ND1 pseudogene 11provided by HGNC
Primary source
HGNC:HGNC:42060
See related
Ensembl:ENSG00000228166 AllianceGenome:HGNC:42060
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:
9p24.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (5094100..5095016)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (5099186..5100102)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (5094100..5095016)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene Janus kinase 2 Neighboring gene insulin like 6 Neighboring gene MT-ND5 pseudogene 36 Neighboring gene MT-ND6 pseudogene 5 Neighboring gene MT-ND2 pseudogene 36 Neighboring gene MT-CO1 pseudogene 11

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 pseudogene 11

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_032399.1 

    Range
    101..1017
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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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    5094100..5095016
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    5099186..5100102
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)