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RN7SL870P RNA, 7SL, cytoplasmic 870, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481155, updated on 12-Oct-2019

Summary

Official Symbol
RN7SL870Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 870, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46886
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 RN7SL870P in Genome Data Viewer
Location:
3p21.31
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (47560229..47560524, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene bolA family member 2 pseudogene 2 Neighboring gene elongator acetyltransferase complex subunit 6 Neighboring gene uncharacterized LOC105377074 Neighboring gene chondroitin sulfate proteoglycan 5 Neighboring gene SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 1 Neighboring gene small nucleolar RNA, C/D box 146

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000003.12 Chromosome 3 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_042927.1 

    Range
    101..396
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    47560229..47560524 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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