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KRT18P36 keratin 18 pseudogene 36 [ Homo sapiens (human) ]

Gene ID: 442406, updated on 17-Sep-2024

Summary

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Official Symbol
KRT18P36provided by HGNC
Official Full Name
keratin 18 pseudogene 36provided by HGNC
Primary source
HGNC:HGNC:33405
See related
Ensembl:ENSG00000226246 AllianceGenome:HGNC:33405
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

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See KRT18P36 in Genome Data Viewer
Location:
9p21.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (30799658..30800798, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (30815285..30816425, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (30799656..30800796, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene RBMX pseudogene 2 Neighboring gene keratin 18 pseudogene 66 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:30790342-30790842 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:30790843-30791343 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_107933 Neighboring gene ribosomal protein S26 pseudogene 2 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:30913207-30913990 Neighboring gene ferritin light chain pseudogene 4

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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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_006016.6 

    Range
    101..1241
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    30799658..30800798 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    30815285..30816425 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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