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RNA5SP302 RNA, 5S ribosomal pseudogene 302 [ Homo sapiens (human) ]

Gene ID: 106479004, updated on 13-May-2022

Summary

Official Symbol
RNA5SP302provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 302provided by HGNC
Primary source
HGNC:HGNC:43202
See related
Ensembl:ENSG00000201766 AllianceGenome:HGNC:43202
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
RN5S302
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Genomic context

See RNA5SP302 in Genome Data Viewer
Location:
10p13
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (14663395..14663494, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (14677413..14677512, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (14705394..14705493, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene family with sequence similarity 107 member B Neighboring gene Sharpr-MPRA regulatory region 15534 Neighboring gene uncharacterized LOC105376429 Neighboring gene ribosomal protein SA pseudogene 7 Neighboring gene cerebral dopamine neurotrophic factor

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_045723.1 

    Range
    101..200
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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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    14663395..14663494 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    14677413..14677512 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)