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COX6CP3 cytochrome c oxidase subunit 6C pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 100130247, updated on 13-May-2022

Summary

Official Symbol
COX6CP3provided by HGNC
Official Full Name
cytochrome c oxidase subunit 6C pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:31721
See related
AllianceGenome:HGNC:31721
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

See COX6CP3 in Genome Data Viewer
Location:
18p11.32
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (1176650..1177072, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (1330923..1331345, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (1176651..1177073, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985165 Neighboring gene uncharacterized LOC105371953 Neighboring gene solute carrier family 25 member 3 pseudogene 3 Neighboring gene Sharpr-MPRA regulatory region 5202 Neighboring gene long intergenic non-protein coding RNA 470 Neighboring gene RN7SK pseudogene 72

Genomic regions, transcripts, and products

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_012734.1 

    Range
    101..523
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000018.10 Reference GRCh38.p14 Primary Assembly

    Range
    1176650..1177072 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    1330923..1331345 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)