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KRT8P11 keratin 8 pseudogene 11 [ Homo sapiens (human) ]

Gene ID: 347265, updated on 29-Mar-2023

Summary

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Official Symbol
KRT8P11provided by HGNC
Official Full Name
keratin 8 pseudogene 11provided by HGNC
Primary source
HGNC:HGNC:31058
See related
Ensembl:ENSG00000255815 AllianceGenome:HGNC:31058
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
KRT8L1
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Genomic context

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See KRT8P11 in Genome Data Viewer
Location:
9q22.33
Annotation release Status Assembly Chr Location
RS_2023_03 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (99305084..99306851)
RS_2023_03 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (111476769..111478536)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (102067366..102069133)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902230 Neighboring gene RN7SK pseudogene 225 Neighboring gene uncharacterized LOC124902231 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:102068645-102069144 Neighboring gene uncharacterized LOC124902232 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:102131371-102131952 Neighboring gene non-protein coding RNA, associated with MAP kinase pathway and growth arrest Neighboring gene uncharacterized LOC107987011 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr9:102181342-102182541

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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Other Names

  • KRT8 pseudogene
  • keratin 8-like 1

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_005157.5 

    Range
    101..1868
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_03

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    99305084..99306851
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    111476769..111478536
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001024612.1: Suppressed sequence

    Description
    NM_001024612.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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