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KRT18P17 keratin 18 pseudogene 17 [ Homo sapiens (human) ]

Gene ID: 344866, updated on 23-Nov-2021

Summary

Official Symbol
KRT18P17provided by HGNC
Official Full Name
keratin 18 pseudogene 17provided by HGNC
Primary source
HGNC:HGNC:33385
See related
Ensembl:ENSG00000213943
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 KRT18P17 in Genome Data Viewer
Location:
3p25.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (12787335..12788720, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (12828834..12830219, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene cysteine rich protein 1 pseudogene 1 Neighboring gene transmembrane protein 40 Neighboring gene cullin associated and neddylation dissociated 2 (putative) Neighboring gene small nucleolar RNA, H/ACA box 7A Neighboring gene ribosomal protein L32

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_009663.3 

    Range
    101..1486
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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_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    12787335..12788720 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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