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KRT18P60 keratin 18 pseudogene 60 [ Homo sapiens (human) ]

Gene ID: 100418829, updated on 23-Nov-2021

Summary

Official Symbol
KRT18P60provided by HGNC
Official Full Name
keratin 18 pseudogene 60provided by HGNC
Primary source
HGNC:HGNC:48887
See related
Ensembl:ENSG00000215208
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 KRT18P60 in Genome Data Viewer
Location:
12q14.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (65418667..65420069, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (65812447..65813849, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene apolipoprotein O pseudogene 3 Neighboring gene LEM domain containing 3 Neighboring gene methionine sulfoxide reductase B3 Neighboring gene uncharacterized LOC105369809 Neighboring gene MSRB3 antisense RNA 1 Neighboring gene uncharacterized LOC105369187 Neighboring gene uncharacterized LOC105369808

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_024029.3 

    Range
    101..1503
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    65418667..65420069 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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