Format

Send to:

Choose Destination

RN7SL749P RNA, 7SL, cytoplasmic 749, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479494, updated on 23-Nov-2021

Summary

Official Symbol
RN7SL749Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 749, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46765
See related
Ensembl:ENSG00000242853
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See RN7SL749P in Genome Data Viewer
Location:
10q26.11
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (119212857..119213146)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (120972369..120972658)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene Sharpr-MPRA regulatory region 12134 Neighboring gene GRK5 intronic transcript 1 Neighboring gene Sharpr-MPRA regulatory region 13114 Neighboring gene G protein-coupled receptor kinase 5 Neighboring gene Sharpr-MPRA regulatory region 9266

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_045657.1 

    Range
    101..390
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    119212857..119213146
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center