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RN7SL751P RNA, 7SL, cytoplasmic 751, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479495, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL751Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 751, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46767
See related
Ensembl:ENSG00000240964 AllianceGenome:HGNC:46767
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 RN7SL751P in Genome Data Viewer
Location:
3p12.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (78938009..78938292, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (78992862..78993145, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (78987159..78987442, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:78630276-78631137 Neighboring gene mitochondrial ribosomal protein S17 pseudogene 3 Neighboring gene roundabout guidance receptor 1 Neighboring gene ribosomal protein S12 pseudogene 6 Neighboring gene Sharpr-MPRA regulatory region 7147 Neighboring gene Sharpr-MPRA regulatory region 6803 Neighboring gene NANOG hESC enhancer GRCh37_chr3:79006574-79007156 Neighboring gene VISTA enhancer hs1475 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:79174827-79175326 Neighboring gene NANOG hESC enhancer GRCh37_chr3:79209960-79210461 Neighboring gene uncharacterized LOC101927374 Neighboring gene microRNA 3923

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_045661.1 

    Range
    101..384
    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
    78938009..78938292 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    78992862..78993145 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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