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RN7SL702P RNA, 7SL, cytoplasmic 702, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481114, updated on 10-Oct-2023

Summary

Official Symbol
RN7SL702Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 702, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46718
See related
Ensembl:ENSG00000243980 AllianceGenome:HGNC:46718
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

Location:
Yq11.21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (12273493..12273762)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (13180921..13181190)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (14394197..14394466)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene ribosomal protein S24 pseudogene 1 Neighboring gene arylsulfatase F pseudogene 1 Neighboring gene AZFa HERV15yq1 recombination region Neighboring gene family with sequence similarity 8, member A1 pseudogene Neighboring gene arylsulfatase L pseudogene 1

Genomic regions, transcripts, and products

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_044637.1 

    Range
    101..370
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    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_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    12273493..12273762
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    13180921..13181190
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)