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RN7SL515P RNA, 7SL, cytoplasmic 515, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481063, updated on 17-Aug-2024

Summary

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Official Symbol
RN7SL515Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 515, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46531
See related
Ensembl:ENSG00000241406 AllianceGenome:HGNC:46531
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See RN7SL515P in Genome Data Viewer
Location:
13q14.11
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (41807677..41807942)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (41026800..41027065)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (42381813..42382078)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370174 Neighboring gene uncharacterized LOC105370175 Neighboring gene ReSE screen-validated silencer GRCh37_chr13:42127997-42128188 Neighboring gene microRNA 5006 Neighboring gene Sharpr-MPRA regulatory region 5362 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:42188550-42189542 Neighboring gene von Willebrand factor A domain containing 8 Neighboring gene FOXA motif-containing MPRA enhancer 169 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5292 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr13:42376466-42377665 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7633 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7634 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7635 Neighboring gene RNA, U6 small nuclear 74, pseudogene Neighboring gene lysyl-tRNA synthetase 1 pseudogene 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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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_044218.1 

    Range
    101..366
    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    41807677..41807942
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    41026800..41027065
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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