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RN7SL457P RNA, 7SL, cytoplasmic 457, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481047, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL457Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 457, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46473
See related
Ensembl:ENSG00000263794 AllianceGenome:HGNC:46473
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:
8p12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (33715784..33716070)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (33987064..33987350)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (33573302..33573588)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:33455207-33455707 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:33483387-33484244 Neighboring gene dual specificity phosphatase 26 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:33515643-33516297 Neighboring gene BUD31 homolog pseudogene 1 Neighboring gene VENT homeobox pseudogene 5 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr8:33612557-33613756 Neighboring gene uncharacterized LOC105379364 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:33715229-33715729 Neighboring gene ribosomal protein L6 pseudogene 22

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_044103.1 

    Range
    101..387
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    33715784..33716070
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    33987064..33987350
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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