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    KRT18P21 keratin 18 pseudogene 21 [ Homo sapiens (human) ]

    Gene ID: 132391, updated on 17-Sep-2024

    Summary

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    Official Symbol
    KRT18P21provided by HGNC
    Official Full Name
    keratin 18 pseudogene 21provided by HGNC
    Primary source
    HGNC:HGNC:33389
    See related
    Ensembl:ENSG00000250363 AllianceGenome:HGNC:33389
    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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    See KRT18P21 in Genome Data Viewer
    Location:
    4q26
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (115920657..115922033)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (119223656..119225033)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (116841813..116843189)

    Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene ribosome production factor 2 homolog pseudogene 2 Neighboring gene phosphoglycerate mutase family member 4 pseudogene 2 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:116732756-116733256 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21843 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:116894806-116895469 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr4:116896911-116897752 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:116899658-116900158 Neighboring gene eukaryotic translation initiation factor 3 subunit K pseudogene 3 Neighboring gene RLF pseudogene 1

    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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    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_009667.1 

      Range
      101..1477
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      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

      Range
      115920657..115922033
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      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060928.1 Alternate T2T-CHM13v2.0

      Range
      119223656..119225033
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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