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

Gene ID: 132391, updated on 10-Oct-2023

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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Location:
4q26
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (115920657..115922033)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (119223656..119225033)
105.20220307 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
    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    115920657..115922033
    Download
    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

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