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RN7SL722P RNA, 7SL, cytoplasmic 722, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479486, updated on 10-Oct-2023

Summary

Official Symbol
RN7SL722Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 722, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46738
See related
Ensembl:ENSG00000273940 AllianceGenome:HGNC:46738
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:
9q13
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (61789143..61789426)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (41715495..41715778, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379437 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:44767663-44768162 Neighboring gene family with sequence similarity 242 member D Neighboring gene uncharacterized LOC105379807 Neighboring gene family with sequence similarity 27 member E4 Neighboring gene family with sequence similarity 27 member C

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_043909.1 

    Range
    101..384
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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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    61789143..61789426
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    41715495..41715778 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)