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RN7SL865P RNA, 7SL, cytoplasmic 865, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481154, updated on 11-Sep-2019

Summary

Official Symbol
RN7SL865Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 865, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46881
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See RN7SL865P in Genome Data Viewer
Location:
12q24.21
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (115717725..115718013)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370003 Neighboring gene uncharacterized LOC105370002 Neighboring gene ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 7 Neighboring gene long intergenic non-protein coding RNA 2463 Neighboring gene mediator complex subunit 13L Neighboring gene RNA, U6 small nuclear 1188, pseudogene

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000012.12 Chromosome 12 Reference GRCh38.p13 Primary Assembly

NCBI Reference Sequences (RefSeq)

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_042917.1 

    Range
    101..389
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109 details...Open this link in a new tab

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    115717725..115718013
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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