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RNU2-71P RNA, U2 small nuclear 71, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480228, updated on 10-Oct-2023

Summary

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Official Symbol
RNU2-71Pprovided by HGNC
Official Full Name
RNA, U2 small nuclear 71, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48564
See related
Ensembl:ENSG00000223327 AllianceGenome:HGNC:48564
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 RNU2-71P in Genome Data Viewer
Location:
8q21.13
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (80585590..80585781, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (81017182..81017373, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (81497825..81498016, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene RNA, U7 small nuclear 174 pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr8:81475570-81476230 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:81477806-81478340 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:81478341-81478873 Neighboring gene OCIA domain containing 2 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19325 Neighboring gene SLC25A51 pseudogene 3 Neighboring gene RNA, 7SL, cytoplasmic 107, pseudogene

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)

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_043716.1 

    Range
    101..292
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    80585590..80585781 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    81017182..81017373 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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