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SNORD13P3 small nucleolar RNA, C/D box 13 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 6078, updated on 12-Oct-2019

Summary

Official Symbol
SNORD13P3provided by HGNC
Official Full Name
small nucleolar RNA, C/D box 13 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:10112
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
U13; U13.4B; RNU13P3

Genomic context

See SNORD13P3 in Genome Data Viewer
Location:
3p21.31
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (47250525..47250626, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (47292015..47292116, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene mitochondrial ribosomal protein L57 pseudogene 3 Neighboring gene SET domain containing 2, histone lysine methyltransferase Neighboring gene KIF9 antisense RNA 1 Neighboring gene kinesin family member 9 Neighboring gene small nucleolar RNA, C/D box 13J Neighboring gene kelch like family member 18 Neighboring gene protein tyrosine phosphatase non-receptor type 23

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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_008261.1 

    Range
    101..202
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    47250525..47250626 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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