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RN7SL508P RNA, 7SL, cytoplasmic 508, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481061, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL508Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 508, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46524
See related
Ensembl:ENSG00000244112 AllianceGenome:HGNC:46524
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:
12q24.23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (118993857..118994159)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (118981355..118981657)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (119431662..119431964)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370019 Neighboring gene small nucleolar RNA SNORA38 Neighboring gene uncharacterized LOC105370020 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:119423722-119424248 Neighboring gene serine/arginine repetitive matrix 4 Neighboring gene uncharacterized LOC105370022 Neighboring gene NANOG hESC enhancer GRCh37_chr12:119493434-119493935 Neighboring gene MPRA-validated peak1997 silencer Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:119526455-119527045 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:119527046-119527635 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:119527912-119528566 Neighboring gene uncharacterized LOC105370021

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_045761.1 

    Range
    101..403
    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_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    118993857..118994159
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    118981355..118981657
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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