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RN7SL397P RNA, 7SL, cytoplasmic 397, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479369, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL397Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 397, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46413
See related
Ensembl:ENSG00000244139 AllianceGenome:HGNC:46413
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:
3q13.33
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (120121909..120122206)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (122841586..122841883)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (119840756..119841053)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20330 Neighboring gene GSK3B divergent transcript Neighboring gene RNA, 7SL, cytoplasmic 762, pseudogene Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr3:119863928-119865127 Neighboring gene uncharacterized LOC105374065 Neighboring gene ReSE screen-validated silencer GRCh37_chr3:119889176-119889400 Neighboring gene G protein-coupled receptor 156 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr3:119961559-119962758 Neighboring gene uncharacterized LOC124909418

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_042971.1 

    Range
    101..398
    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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    120121909..120122206
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    122841586..122841883
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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