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KRT8P41 keratin 8 pseudogene 41 [ Homo sapiens (human) ]

Gene ID: 283102, updated on 23-Nov-2021

Summary

Official Symbol
KRT8P41provided by HGNC
Official Full Name
keratin 8 pseudogene 41provided by HGNC
Primary source
HGNC:HGNC:39875
See related
Ensembl:ENSG00000213538
Gene type
pseudo
RefSeq status
VALIDATED
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 KRT8P41 in Genome Data Viewer
Location:
11p15.4
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (9094363..9096190)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (9115910..9117737)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene nuclear receptor interacting protein 3 Neighboring gene NRIP3 divergent transcript Neighboring gene signal peptide, CUB domain and EGF like domain containing 2 Neighboring gene microRNA 5691 Neighboring gene uncharacterized LOC105376542 Neighboring gene Sharpr-MPRA regulatory region 9656 Neighboring gene DENN domain containing 5A

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_027713.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC079296
    Related
    ENST00000533985.1

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_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    9094363..9096190
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_005658.3: Suppressed sequence

    Description
    NG_005658.3: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
  2. NG_024464.1: Suppressed sequence

    Description
    NG_024464.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is transcribed.
  3. NM_198473.1: Suppressed sequence

    Description
    NM_198473.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
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