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RNA5SP512 RNA, 5S ribosomal pseudogene 512 [ Homo sapiens (human) ]

Gene ID: 100873563, updated on 12-Oct-2019

Summary

Official Symbol
RNA5SP512provided by HGNC
Official Full Name
RNA, 5S ribosomal pseudogene 512provided by HGNC
Primary source
HGNC:HGNC:43412
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
RN5S512

Genomic context

See RNA5SP512 in Genome Data Viewer
Location:
Xq23
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (111669829..111669948, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein L18a pseudogene 15 Neighboring gene eukaryotic translation initiation factor 4B pseudogene 7 Neighboring gene ALG13 UDP-N-acetylglucosaminyltransferase subunit Neighboring gene transient receptor potential cation channel subfamily C member 5 Neighboring gene TRPC5 opposite strand

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000023.11 Chromosome X Reference GRCh38.p13 Primary Assembly

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_033418.1 

    Range
    101..220
    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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    111669829..111669948 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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