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RNA5SP327 RNA, 5S ribosomal pseudogene 327 [ Homo sapiens (human) ]

Gene ID: 100873593, updated on 13-May-2022

Summary

Official Symbol
RNA5SP327provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 327provided by HGNC
Primary source
HGNC:HGNC:43227
See related
Ensembl:ENSG00000199364 AllianceGenome:HGNC:43227
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
RN5S327
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Genomic context

See RNA5SP327 in Genome Data Viewer
Location:
10q25.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (110761142..110761242)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (111644900..111645000)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (112520900..112521000)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene RNA binding motif protein 20 Neighboring gene uncharacterized LOC124902498 Neighboring gene RN7SK pseudogene 288 Neighboring gene uncharacterized LOC124902499 Neighboring gene CRISPRi-validated cis-regulatory element chr10.4148 Neighboring gene uncharacterized LOC124902500

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_033476.1 

    Range
    101..201
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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
    110761142..110761242
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    111644900..111645000
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)