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KRT19P2 keratin 19 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 160313, updated on 13-May-2022

Summary

Official Symbol
KRT19P2provided by HGNC
Official Full Name
keratin 19 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:33423
See related
Ensembl:ENSG00000216306 AllianceGenome:HGNC:33423
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
KRT19P5
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Genomic context

See KRT19P2 in Genome Data Viewer
Location:
12q22
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (94834454..94835028)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (94815326..94815900)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (95228230..95228804)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene transmembrane and coiled-coil domain family 3 Neighboring gene uncharacterized LOC105369914 Neighboring gene uncharacterized LOC124902989 Neighboring gene microRNA 492 Neighboring gene uncharacterized LOC105369915 Neighboring gene NADH:ubiquinone oxidoreductase subunit A12

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.

RNA

  1. NR_036685.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AB041269, AC117494
    Related
    ENST00000405395.2

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    94834454..94835028
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    94815326..94815900
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_002383.2: Suppressed sequence

    Description
    NG_002383.2: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.