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RRN3P3 RRN3 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 100131998, updated on 25-Oct-2022

Summary

Official Symbol
RRN3P3provided by HGNC
Official Full Name
RRN3 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:37620
See related
Ensembl:ENSG00000290865 AllianceGenome:HGNC:37620
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Ubiquitous expression in bone marrow (RPKM 2.9), thyroid (RPKM 2.8) and 25 other tissues See more
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Genomic context

See RRN3P3 in Genome Data Viewer
Location:
16p12.2
Exon count:
7
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (22418672..22437461, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (21779755..21798544)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (22429993..22448782, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene CDR2 divergent transcript Neighboring gene major facilitator superfamily domain containing 13B (pseudogene) Neighboring gene SMG1 pseudogene 1 Neighboring gene small nucleolar RNA U13 Neighboring gene uncharacterized LOC105371131 Neighboring gene nuclear pore complex interacting protein family member B5

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Other Names

  • RNA polymerase I transcription factor homolog pseudogene 3
  • RRN3 RNA polymerase I transcription factor homolog pseudogene
  • RRN3 homolog, RNA polymerase I transcription factor pseudogene 3

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.

RNA

  1. NR_027460.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC092338, AC106788
    Related
    ENST00000551766.5

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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    22418672..22437461 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_017852933.1 Reference GRCh38.p14 PATCHES

    Range
    667578..686367
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    21779755..21798544
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)