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RN7SL607P RNA, 7SL, cytoplasmic 607, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481088, updated on 1-Aug-2020

Summary

Official Symbol
RN7SL607Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 607, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46623
See related
Ensembl:ENSG00000278525
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 RN7SL607P in Genome Data Viewer
Location:
20p11.23
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 20 NC_000020.11 (20738433..20738731, complement)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 2040 Neighboring gene uncharacterized LOC105372555 Neighboring gene LLPH pseudogene 1 Neighboring gene mitochondrial ribosomal protein S11 pseudogene 1 Neighboring gene Sharpr-MPRA regulatory region 9877 Neighboring gene long intergenic non-protein coding RNA 237

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000020.11 Chromosome 20 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_044430.1 

    Range
    101..399
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20200522

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p13 Primary Assembly

    Range
    20738433..20738731 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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