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KRT18P44 keratin 18 pseudogene 44 [ Homo sapiens (human) ]

Gene ID: 139748, updated on 13-May-2022

Summary

Official Symbol
KRT18P44provided by HGNC
Official Full Name
keratin 18 pseudogene 44provided by HGNC
Primary source
HGNC:HGNC:33414
See related
Ensembl:ENSG00000218728 AllianceGenome:HGNC:33414
Gene type
pseudo
RefSeq status
INFERRED
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 KRT18P44 in Genome Data Viewer
Location:
Xq25
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (128714456..128715830)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (127032543..127033917)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (127848434..127849808)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985698 Neighboring gene ribosomal protein L7a pseudogene 72 Neighboring gene RUVBL2 pseudogene 1 Neighboring gene uncharacterized LOC107985699 Neighboring gene ribosomal protein L32 pseudogene 35

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.

Genomic

  1. NG_008310.3 

    Range
    101..1475
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    GenBank, FASTA, Sequence Viewer (Graphics)

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    128714456..128715830
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    127032543..127033917
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)