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RN7SL107P RNA, 7SL, cytoplasmic 107, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479262, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL107Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 107, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46123
See related
Ensembl:ENSG00000243424 AllianceGenome:HGNC:46123
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:
8q21.13
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (80613538..80613816, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (81045132..81045410, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (81525773..81526051, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene RNA, U2 small nuclear 71, pseudogene Neighboring gene SLC25A51 pseudogene 3 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:81552571-81553770 Neighboring gene zinc finger protein 704 Neighboring gene CDC28 protein kinase regulatory subunit 1B pseudogene 7 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:81610513-81611014 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:81611015-81611514 Neighboring gene RNA, U11 small nuclear 6, pseudogene

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_044149.1 

    Range
    101..379
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    80613538..80613816 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    81045132..81045410 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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