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RN7SL270P RNA, 7SL, cytoplasmic 270, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480995, updated on 29-Mar-2018

Summary

Official Symbol
RN7SL270Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 270, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46286
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 RN7SL270P in Genome Data Viewer
Location:
17q21.32
Annotation release Status Assembly Chr Location
109 current GRCh38.p12 (GCF_000001405.38) 17 NC_000017.11 (47041729..47042204)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene leucine rich repeat containing 37 member A2 Neighboring gene uncharacterized LOC101927060 Neighboring gene golgi SNAP receptor complex member 2 Neighboring gene microRNA 5089 Neighboring gene leucine rich repeat containing 37 member A17, pseudogene Neighboring gene reprimo like Neighboring gene protein GVQW1-like Neighboring gene cell division cycle 27 Neighboring gene ribosomal protein S2 pseudogene 47

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000017.11 Chromosome 17 Reference GRCh38.p12 Primary Assembly

Bibliography

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

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_046319.1 

    Range
    101..576
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

Reference GRCh38.p12 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p12 Primary Assembly

    Range
    47041729..47042204
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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