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RN7SL408P RNA, 7SL, cytoplasmic 408, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481841, updated on 4-Mar-2025

Summary

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Official Symbol
RN7SL408Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 408, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46424
See related
Ensembl:ENSG00000266875 AllianceGenome:HGNC:46424
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 RN7SL408P in Genome Data Viewer
Location:
6q23.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (134133573..134133868)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (135321497..135321792)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (134454711..134455006)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene epithelial splicing regulatory protein 1 pseudogene Neighboring gene solute carrier family 2 member 12 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr6:134381498-134382162 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:134382163-134382827 Neighboring gene uncharacterized LOC124901404 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17556 Neighboring gene high mobility group AT-hook 1 pseudogene 7 Neighboring gene NANOG hESC enhancer GRCh37_chr6:134481640-134482141 Neighboring gene H3K27ac hESC enhancer GRCh37_chr6:134496091-134496592 Neighboring gene Sharpr-MPRA regulatory region 71 Neighboring gene serum/glucocorticoid regulated kinase 1 Neighboring gene small nucleolar RNA U13 Neighboring gene ribosomal protein S29 pseudogene 32

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_045796.1 

    Range
    101..396
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    134133573..134133868
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    135321497..135321792
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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