U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

RNU5F-8P RNA, U5F small nuclear 8, pseudogene [ Homo sapiens (human) ]

Gene ID: 100873839, updated on 10-Oct-2023

Summary

Go to the top of the page Help
Official Symbol
RNU5F-8Pprovided by HGNC
Official Full Name
RNA, U5F small nuclear 8, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:42531
See related
Ensembl:ENSG00000251750 AllianceGenome:HGNC:42531
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 RNU5F-8P in Genome Data Viewer
Location:
1q43
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (240653367..240653477)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (240064780..240064890)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (240816667..240816777)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene gremlin 2, DAN family BMP antagonist Neighboring gene uncharacterized LOC124904600 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:240770159-240770658 Neighboring gene ribosomal protein S11 pseudogene 2 Neighboring gene ferredoxin 2 pseudogene Neighboring gene uncharacterized LOC105373228 Neighboring gene Sharpr-MPRA regulatory region 3663

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)

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_032619.1 

    Range
    101..211
    Download
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    240653367..240653477
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    240064780..240064890
    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