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RN7SKP189 RN7SK pseudogene 189 [ Homo sapiens (human) ]

Gene ID: 106479180, updated on 10-Oct-2023

Summary

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Official Symbol
RN7SKP189provided by HGNC
Official Full Name
RN7SK pseudogene 189provided by HGNC
Primary source
HGNC:HGNC:45913
See related
AllianceGenome:HGNC:45913
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:
Xq27.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (145057108..145057347)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (143316010..143316249)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (144138628..144138867)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ribonucleotide reductase M2 polypeptide pseudogene 4 Neighboring gene NANOG hESC enhancer GRCh37_chrX:143834881-143835457 Neighboring gene NANOG hESC enhancer GRCh37_chrX:143855361-143855862 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:143882879-143884078 Neighboring gene heterogeneous nuclear ribonucleoprotein C pseudogene 10 Neighboring gene CYCS pseudogene 44 Neighboring gene SPANX family member N1

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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Other Names

  • RNA, 7SK small nuclear pseudogene 189

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_043528.1 

    Range
    101..340
    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
    145057108..145057347
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    143316010..143316249
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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