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RN7SL795P RNA, 7SL, cytoplasmic 795, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479511, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL795Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 795, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46811
See related
Ensembl:ENSG00000239748 AllianceGenome:HGNC:46811
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 RN7SL795P in Genome Data Viewer
Location:
18q22.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (70512727..70512997)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (70734447..70734717)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (68179963..68180233)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_49413 Neighboring gene ribosomal protein S2 pseudogene 6 Neighboring gene uncharacterized LOC105376872 Neighboring gene H3K27ac hESC enhancer GRCh37_chr18:68237381-68237880 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 13487 Neighboring gene Gilles de la Tourette syndrome chromosome region, candidate 1 Neighboring gene uncharacterized LOC124904322

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_044097.1 

    Range
    101..371
    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_000018.10 Reference GRCh38.p14 Primary Assembly

    Range
    70512727..70512997
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    70734447..70734717
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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