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RN7SL822P RNA, 7SL, cytoplasmic 822, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479521, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL822Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 822, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46838
See related
Ensembl:ENSG00000239545 AllianceGenome:HGNC:46838
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:
4q12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (55215624..55215919, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (58703735..58704030, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (56081791..56082086, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene RNA, 7SL, cytoplasmic 424, pseudogene Neighboring gene Sharpr-MPRA regulatory region 1754 Neighboring gene kinase insert domain receptor Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr4:55998829-55999442 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr4:56035898-56036727 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr4:56041662-56042861 Neighboring gene METTL5 pseudogene 3 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:56107314-56107814 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:56107815-56108315 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:56146057-56147004 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:56147005-56147952 Neighboring gene RNA, U6 small nuclear 746, 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_044171.1 

    Range
    101..396
    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    55215624..55215919 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    58703735..58704030 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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