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RN7SL799P RNA, 7SL, cytoplasmic 799, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480382, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL799Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 799, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46815
See related
Ensembl:ENSG00000244006 AllianceGenome:HGNC:46815
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:
Xq11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (64210691..64210988)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (62635966..62636263)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (63430571..63430868)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene zinc finger protein 670 pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chrX:63372768-63373287 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20877 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20878 Neighboring gene uncharacterized LOC112268307 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29708 Neighboring gene APC membrane recruitment protein 1 Neighboring gene ankyrin repeat and SOCS box containing 12 Neighboring gene myotubularin related protein 8 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:63521683-63522184 Neighboring gene KPNA4 pseudogene 1

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_044922.1 

    Range
    101..398
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    64210691..64210988
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    62635966..62636263
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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