Format

Send to:

Choose Destination

KRT8P19 keratin 8 pseudogene 19 [ Homo sapiens (human) ]

Gene ID: 644998, updated on 23-Nov-2021

Summary

Official Symbol
KRT8P19provided by HGNC
Official Full Name
keratin 8 pseudogene 19provided by HGNC
Primary source
HGNC:HGNC:33371
See related
Ensembl:ENSG00000257528
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See KRT8P19 in Genome Data Viewer
Location:
12q14.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (61879244..61880972)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (62273025..62274753)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105369793 Neighboring gene TAFA chemokine like family member 2 Neighboring gene ribosomal protein L21 pseudogene 104 Neighboring gene ribosomal protein S3 pseudogene 6 Neighboring gene Kruppel like factor 17 pseudogene 1

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_009706.1 

    Range
    101..1829
    Download
    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
    61879244..61880972
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center