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RNA5SP412 RNA, 5S ribosomal pseudogene 412 [ Homo sapiens (human) ]

Gene ID: 100873663, updated on 10-Oct-2023

Summary

Official Symbol
RNA5SP412provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 412provided by HGNC
Primary source
HGNC:HGNC:43312
See related
Ensembl:ENSG00000277004 AllianceGenome:HGNC:43312
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
RN5S412
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Genomic context

Location:
16p11.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (35746772..35746894)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (38381661..38381783, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (34981143..34981265)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene RNA, 5S ribosomal pseudogene 410 Neighboring gene RNA, 5S ribosomal pseudogene 411 Neighboring gene long intergenic non-protein coding RNA 2167 Neighboring gene RNA, 5S ribosomal pseudogene 413 Neighboring gene RNA, 5S ribosomal pseudogene 414

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_033598.1 

    Range
    101..223
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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
    35746772..35746894
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    38381661..38381783 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)