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KRT8P32 keratin 8 pseudogene 32 [ Homo sapiens (human) ]

Gene ID: 100289133, updated on 10-Oct-2023

Summary

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Official Symbol
KRT8P32provided by HGNC
Official Full Name
keratin 8 pseudogene 32provided by HGNC
Primary source
HGNC:HGNC:39866
See related
Ensembl:ENSG00000250221 AllianceGenome:HGNC:39866
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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Location:
5q15
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (98391816..98393610, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (98895035..98896829, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (97727520..97729314, complement)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene proteasome activator subunit 2 pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr5:97674143-97674644 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr5:97678603-97679104 Neighboring gene actin beta pseudogene Neighboring gene Sharpr-MPRA regulatory region 1674 Neighboring gene mitochondrial ribosomal protein S35 pseudogene 2 Neighboring gene MT-CO2 pseudogene 24

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_021858.2 

    Range
    101..1895
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    98391816..98393610 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    98895035..98896829 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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