U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

KRT18P68 keratin 18 pseudogene 68 [ Homo sapiens (human) ]

Gene ID: 139060, updated on 17-Sep-2024

Summary

Go to the top of the page Help
Official Symbol
KRT18P68provided by HGNC
Official Full Name
keratin 18 pseudogene 68provided by HGNC
Primary source
HGNC:HGNC:48895
See related
Ensembl:ENSG00000213100 AllianceGenome:HGNC:48895
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

Go to the top of the page Help
See KRT18P68 in Genome Data Viewer
Location:
Xp11.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (45983315..45984369)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (45390705..45391759)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (45842750..45843804)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene SRSF6 pseudogene 1 Neighboring gene mediator complex subunit 28 pseudogene 4 Neighboring gene proliferating cell nuclear antigen pseudogene 3 Neighboring gene NANOG hESC enhancer GRCh37_chrX:46114084-46114585 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:46122614-46123813 Neighboring gene ACTB pseudogene 1

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to nucleotide: Graphics FASTA GenBank

Bibliography

Go to the top of the pageHelp

GeneRIFs: Gene References Into Functions

Phenotypes

Go to the top of the page Help

Review eQTL and phenotype association data in this region using PheGenI

Variation

Go to the top of the page Help

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

Go to the top of the page Help

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

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_029275.2 

    Range
    101..1155
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    45983315..45984369
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    45390705..45391759
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases
Research Materials