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    CYCSP23 CYCS pseudogene 23 [ Homo sapiens (human) ]

    Gene ID: 360176, updated on 10-Oct-2023

    Summary

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    Official Symbol
    CYCSP23provided by HGNC
    Official Full Name
    CYCS pseudogene 23provided by HGNC
    Primary source
    HGNC:HGNC:24397
    See related
    Ensembl:ENSG00000253495 AllianceGenome:HGNC:24397
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HCP23
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    Genomic context

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    Location:
    8q24.12
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (119618156..119618474, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (120747021..120747339, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (120630396..120630714, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene NANOG hESC enhancer GRCh37_chr8:120437890-120438632 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr8:120450916-120452115 Neighboring gene cellular communication network factor 3 Neighboring gene zinc finger protein 532 pseudogene Neighboring gene Sharpr-MPRA regulatory region 15323 Neighboring gene ectonucleotide pyrophosphatase/phosphodiesterase 2 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:120609160-120609857 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19482 Neighboring gene Sharpr-MPRA regulatory region 2988 Neighboring gene uncharacterized LOC105375727 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:120684845-120685448 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:120685449-120686051 Neighboring gene RN7SK pseudogene 153

    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 human genome has 49 cytochrome c pseudogenes, including a relic of a primordial gene that still functions in mouse. Zhang Z, et al. Gene, 2003 Jul 17. PMID 12909341

    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 Variation Viewer (GRCh37.p13)

    General gene information

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    Other Names

    • cytochrome c, somatic pseudogene 23

    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_002973.2 

      Range
      101..419
      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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      119618156..119618474 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      120747021..120747339 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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