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

Gene ID: 106479494, updated on 13-May-2022

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 AllianceGenome:HGNC:46765
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See RN7SL749P in Genome Data Viewer
Location:
10q26.11
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (119212857..119213146)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (120108260..120108549)
105.20220307 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 peroxiredoxin 3 Neighboring gene Sharpr-MPRA regulatory region 13114 Neighboring gene G protein-coupled receptor kinase 5 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr10:121074255-121075454

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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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
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

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

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    120108260..120108549
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)