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RN7SL60P RNA, 7SL, cytoplasmic 60, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480938, updated on 17-Sep-2024

Summary

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Official Symbol
RN7SL60Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 60, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46076
See related
Ensembl:ENSG00000243366 AllianceGenome:HGNC:46076
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 RN7SL60P in Genome Data Viewer
Location:
13q32.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (98671980..98672278)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (97881964..97882262)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (99324234..99324532)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene CYCS pseudogene 35 Neighboring gene calmodulin 2 pseudogene 4 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7921 Neighboring gene solute carrier family 15 member 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 5461 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:99390337-99390879 Neighboring gene uncharacterized LOC105370330

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_043262.1 

    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    98671980..98672278
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    97881964..97882262
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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