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RN7SL91P RNA, 7SL, cytoplasmic 91, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480946, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SL91Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 91, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46107
See related
Ensembl:ENSG00000240439 AllianceGenome:HGNC:46107
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:
Xp21.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (25060649..25060939, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (24644888..24645178, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (25078766..25079056, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:25022180-25022754 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:25022755-25023328 Neighboring gene aristaless related homeobox polyalanine expansion region Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:25038709-25039287 Neighboring gene PAFAH1B2 pseudogene 1 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:25068048-25068635 Neighboring gene aristaless related homeobox Neighboring gene NANOG hESC enhancer GRCh37_chrX:25148731-25149232 Neighboring gene METTL1 pseudogene 1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:25333172-25333672 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:25333673-25334173 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:25336213-25336714 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:25336715-25337214 Neighboring gene NANOG hESC enhancer GRCh37_chrX:25383902-25384437 Neighboring gene VISTA enhancer hs123 Neighboring gene uncharacterized LOC107985652

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_043329.1 

    Range
    101..391
    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
    25060649..25060939 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    24644888..24645178 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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