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RN7SL808P RNA, 7SL, cytoplasmic 808, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481861, updated on 17-Sep-2024

Summary

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Official Symbol
RN7SL808Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 808, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46824
See related
Ensembl:ENSG00000240637 AllianceGenome:HGNC:46824
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 RN7SL808P in Genome Data Viewer
Location:
4q26
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (114799331..114799629)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (118102326..118102624)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (115720487..115720785)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124900763 Neighboring gene uncharacterized LOC105377382 Neighboring gene CIR1 pseudogene 2 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21841 Neighboring gene ReSE screen-validated silencer GRCh37_chr4:115729032-115729235 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21842 Neighboring gene N-deacetylase and N-sulfotransferase 4 Neighboring gene uncharacterized LOC124900764 Neighboring gene mitochondrial ribosomal protein S33 pseudogene 3

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_044466.1 

    Range
    101..399
    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    114799331..114799629
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    118102326..118102624
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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