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RN7SL824P RNA, 7SL, cytoplasmic 824, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481146, updated on 20-Mar-2020

Summary

Official Symbol
RN7SL824Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 824, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46840
See related
Ensembl:ENSG00000242764
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 RN7SL824P in Genome Data Viewer
Location:
1p22.1
Annotation release Status Assembly Chr Location
109.20200228 current GRCh38.p13 (GCF_000001405.39) 1 NC_000001.11 (92402389..92402685, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene chromosome 1 open reading frame 146 Neighboring gene ACTB pseudogene 12 Neighboring gene glomulin, FKBP associated protein Neighboring gene RNA polymerase II associated protein 2 Neighboring gene growth factor independent 1 transcriptional repressor Neighboring gene ecotropic viral integration site 5 Neighboring gene succinate dehydrogenase assembly factor 3, mitochondrial pseudogene

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000001.11 Chromosome 1 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_044895.1 

    Range
    101..397
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p13 Primary Assembly

    Range
    92402389..92402685 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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