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KRT18P11 keratin 18 pseudogene 11 [ Homo sapiens (human) ]

Gene ID: 3876, updated on 25-Jan-2022

Summary

Official Symbol
KRT18P11provided by HGNC
Official Full Name
keratin 18 pseudogene 11provided by HGNC
Primary source
HGNC:HGNC:6431
See related
Ensembl:ENSG00000215089 AllianceGenome:HGNC:6431
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
KRT18L1
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Genomic context

See KRT18P11 in Genome Data Viewer
Location:
Xq21.31
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (92459611..92461009)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (91714610..91716008)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene protocadherin 11 X-linked Neighboring gene voltage dependent anion channel 1 pseudogene 3 Neighboring gene eukaryotic translation initiation factor 4A1 pseudogene 10 Neighboring gene sorting nexin 3 pseudogene 1 X-linked Neighboring gene ribosomal protein L26 pseudogene 36

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_005219.5 

    Range
    101..1499
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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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    92459611..92461009
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_032934.1: Suppressed sequence

    Description
    NM_032934.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
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