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KRT8P44 keratin 8 pseudogene 44 [ Homo sapiens (human) ]

Gene ID: 100129958, updated on 17-Sep-2024

Summary

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Official Symbol
KRT8P44provided by HGNC
Official Full Name
keratin 8 pseudogene 44provided by HGNC
Primary source
HGNC:HGNC:39878
See related
Ensembl:ENSG00000227913 AllianceGenome:HGNC:39878
Gene type
pseudo
RefSeq status
VALIDATED
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 KRT8P44 in Genome Data Viewer
Location:
6q26
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (162568303..162569966)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (163931425..163933082)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (162989335..162990998)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene parkin RBR E3 ubiquitin protein ligase Neighboring gene uncharacterized LOC105378097 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:162759597-162760144 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:162760145-162760692 Neighboring gene uncharacterized LOC105369171 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:162888287-162888788 Neighboring gene NANOG hESC enhancer GRCh37_chr6:162909371-162909872 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:162952273-162953090 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:162963903-162964402 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:162967043-162967544 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:162967545-162968044 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:163135428-163135928 Neighboring gene ReSE screen-validated silencer GRCh37_chr6:163148405-163148626 Neighboring gene tRNA-Glu (TTC) 15-1 Neighboring gene VISTA enhancer hs1358 Neighboring gene parkin coregulated Neighboring gene ribosomal protein L34 pseudogene 15

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_023305.1 

    Range
    101..1764
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    162568303..162569966
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    163931425..163933082
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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