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CEROX1 cytoplasmic endogenous regulator of oxidative phosphorylation 1 [ Homo sapiens (human) ]

Gene ID: 115804232, updated on 21-Mar-2023

Summary

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Official Symbol
CEROX1provided by HGNC
Official Full Name
cytoplasmic endogenous regulator of oxidative phosphorylation 1provided by HGNC
Primary source
HGNC:HGNC:53928
See related
Ensembl:ENSG00000260807 AllianceGenome:HGNC:53928
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Orthologs
mouse all
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Genomic context

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See CEROX1 in Genome Data Viewer
Location:
16p13.3
Exon count:
5
Annotation release Status Assembly Chr Location
RS_2023_03 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (975761..981613, complement)
RS_2023_03 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (986526..992407, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (1025761..1031613, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene lipase maturation factor 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:1022163-1023153 Neighboring gene uncharacterized LOC124903620 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr16:1038856-1039356 Neighboring gene SRY-box transcription factor 8

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. The long non-coding RNA Cerox1 is a post transcriptional regulator of mitochondrial complex I catalytic activity. Sirey TM, et al. Elife, 2019 May 2. PMID 31045494, Free PMC Article
  2. Normalization and subtraction: two approaches to facilitate gene discovery. Bonaldo MF, et al. Genome Res, 1996 Sep. PMID 8889548
  3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

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 variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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Potential readthrough

Included gene: LMF1

Homology

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.

RNA

  1. NR_036442.3 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC009041, AK125201, BM017667, CK300754, KF456144
    Related
    ENST00000563863.5

  2. NR_164337.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC009041, BC098409
    Related
    ENST00000562570.1

  3. NR_164338.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC009041, KF456144

  4. NR_164339.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC009041, KF456144
    Related
    ENST00000565467.1

  5. NR_164340.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC009041, KF456144
    Related
    ENST00000568394.1

  6. NR_164341.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC009041, KF456144

  7. NR_164342.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC009041, KF456144

  8. NR_164343.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC009041, KF456144

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_03

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    975761..981613 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    986526..992407 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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