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RNU2-16P RNA, U2 small nuclear 16, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481639, updated on 13-May-2022

Summary

Official Symbol
RNU2-16Pprovided by HGNC
Official Full Name
RNA, U2 small nuclear 16, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48509
See related
Ensembl:ENSG00000222644 AllianceGenome:HGNC:48509
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

See RNU2-16P in Genome Data Viewer
Location:
4q21.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (75829454..75829589, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (79169565..79169700, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (76750607..76750742, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene G3BP stress granule assembly factor 2 Neighboring gene USO1 vesicle transport factor Neighboring gene uncharacterized LOC105377284 Neighboring gene uncharacterized LOC105377285 Neighboring gene Sharpr-MPRA regulatory region 11706 Neighboring gene protein phosphatase with EF-hand domain 2 Neighboring gene N-acylethanolamine acid amidase

Genomic regions, transcripts, and products

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_044741.1 

    Range
    101..236
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    75829454..75829589 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    79169565..79169700 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)