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RN7SKP115 RN7SK pseudogene 115 [ Homo sapiens (human) ]

Gene ID: 106479146, updated on 13-May-2022

Summary

Official Symbol
RN7SKP115provided by HGNC
Official Full Name
RN7SK pseudogene 115provided by HGNC
Primary source
HGNC:HGNC:45839
See related
Ensembl:ENSG00000200047 AllianceGenome:HGNC:45839
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

See RN7SKP115 in Genome Data Viewer
Location:
11q22.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (100839630..100839946)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (100848808..100849124)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (100710361..100710677)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene ARHGAP42 antisense RNA 1 Neighboring gene Rho GTPase activating protein 42 Neighboring gene Sharpr-MPRA regulatory region 13184 Neighboring gene uncharacterized LOC105369457 Neighboring gene small nucleolar RNA, C/D box 13I

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_045375.1 

    Range
    101..417
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    100839630..100839946
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    100848808..100849124
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)