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RN7SL659P RNA, 7SL, cytoplasmic 659, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479462, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL659Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 659, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46675
See related
Ensembl:ENSG00000244104 AllianceGenome:HGNC:46675
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 RN7SL659P in Genome Data Viewer
Location:
9q31.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (107811616..107811914, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (119980116..119980414, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (110573897..110574195, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902242 Neighboring gene uncharacterized LOC105376208 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:110500475-110500976 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:110500977-110501476 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:110501606-110502106 Neighboring gene NANOG hESC enhancer GRCh37_chr9:110513433-110514160 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28752 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:110517211-110518410 Neighboring gene uncharacterized LOC105376209 Neighboring gene GATA motif-containing MPRA enhancer 40 Neighboring gene RNA, U6 small nuclear 1064, pseudogene Neighboring gene ribosomal protein L36a pseudogene 6 Neighboring gene small EDRK-rich factor 2-like

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_043731.1 

    Range
    101..399
    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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    107811616..107811914 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    119980116..119980414 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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