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RN7SL869P RNA, 7SL, cytoplasmic 869, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481864, updated on 17-Sep-2024

Summary

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Official Symbol
RN7SL869Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 869, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46885
See related
Ensembl:ENSG00000244392 AllianceGenome:HGNC:46885
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 RN7SL869P in Genome Data Viewer
Location:
7q21.11
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (80245926..80246225)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (81497270..81497569)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (79875242..79875541)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene ribosomal protein L10 pseudogene 11 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr7:79756995-79757534 Neighboring gene G protein subunit alpha i1 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr7:79794160-79794976 Neighboring gene uncharacterized LOC107986743 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:79912787-79913288 Neighboring gene uncharacterized LOC107986744 Neighboring gene RNA, 7SL, cytoplasmic 35, pseudogene

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_044489.1 

    Range
    101..400
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    80245926..80246225
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    81497270..81497569
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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