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RN7SL692P RNA, 7SL, cytoplasmic 692, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479476, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL692Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 692, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46708
See related
Ensembl:ENSG00000239710 AllianceGenome:HGNC:46708
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:
1p22.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (92974827..92975114, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (92820009..92820296, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (93440384..93440671, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene divergent protein kinase domain 1A Neighboring gene MND1 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1321 Neighboring gene Sharpr-MPRA regulatory region 12717 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1322 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:93420065-93420248 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1323 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1078 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1079 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1324 Neighboring gene RNA, U6 small nuclear 970, pseudogene Neighboring gene uncharacterized LOC124904219 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1080 Neighboring gene Sharpr-MPRA regulatory region 610 Neighboring gene Sharpr-MPRA regulatory region 5366 Neighboring gene RNA, U6 small nuclear 210, 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_043840.1 

    Range
    101..388
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    92974827..92975114 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    92820009..92820296 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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