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RN7SL513P RNA, 7SL, cytoplasmic 513, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481062, updated on 20-Mar-2020

Summary

Official Symbol
RN7SL513Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 513, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46529
See related
Ensembl:ENSG00000239821
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See RN7SL513P in Genome Data Viewer
Location:
19p13.11
Annotation release Status Assembly Chr Location
109.20200228 current GRCh38.p13 (GCF_000001405.39) 19 NC_000019.10 (18333276..18333573)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene LSM4 homolog, U6 small nuclear RNA and mRNA degradation associated Neighboring gene Sharpr-MPRA regulatory region 14103 Neighboring gene uncharacterized LOC105372300 Neighboring gene pyroglutamyl-peptidase I Neighboring gene Sharpr-MPRA regulatory region 798 Neighboring gene Sharpr-MPRA regulatory region 10546

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000019.10 Chromosome 19 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_044210.1 

    Range
    101..398
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000019.10 Reference GRCh38.p13 Primary Assembly

    Range
    18333276..18333573
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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