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SNORD3P1 small nucleolar RNA, C/D box 3 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 6068, updated on 23-Nov-2021

Summary

Official Symbol
SNORD3P1provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 3 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:10175
See related
Ensembl:ENSG00000200318
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
U3; RNU3P1
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Genomic context

See SNORD3P1 in Genome Data Viewer
Location:
15q21.3
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (58760466..58760681, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (59052665..59052880, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene ADAM metallopeptidase domain 10 Neighboring gene RN7SK pseudogene 95 Neighboring gene ATP synthase membrane subunit g pseudogene Neighboring gene MINDY2 divergent transcript Neighboring gene MINDY lysine 48 deubiquitinase 2

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Other Names

  • RNA, U3 small nuclear pseudogene 1
  • RNA, U3 small nucleolar pseudogene 1

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_001185.3 

    Range
    101..316
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p13 Primary Assembly

    Range
    58760466..58760681 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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