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RN7SL831P RNA, 7SL, cytoplasmic 831, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481862, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL831Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 831, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46847
See related
Ensembl:ENSG00000241992 AllianceGenome:HGNC:46847
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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Location:
1p21.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (96583209..96583527)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (96431307..96431625)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (97048765..97049083)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene eukaryotic translation elongation factor 1 alpha 1 pseudogene 11 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr1:96940692-96941544 Neighboring gene uncharacterized LOC105378866 Neighboring gene Sharpr-MPRA regulatory region 15484 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:96953857-96954356 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr1:97009971-97010938 Neighboring gene NADH:ubiquinone oxidoreductase subunit S5 pseudogene 2 Neighboring gene ribosomal protein L7 pseudogene 9

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_044475.1 

    Range
    101..419
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    96583209..96583527
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    96431307..96431625
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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