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RN7SL757P RNA, 7SL, cytoplasmic 757, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480530, updated on 13-May-2022

Summary

Official Symbol
RN7SL757Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 757, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46773
See related
Ensembl:ENSG00000239249 AllianceGenome:HGNC:46773
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 RN7SL757P in Genome Data Viewer
Location:
22q12.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (28056153..28056453, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (28517564..28517864, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (28452141..28452441, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene phosphatidylinositol transfer protein beta Neighboring gene TTC28 antisense RNA 1 Neighboring gene microRNA 3199-1 Neighboring gene microRNA 3199-2 Neighboring gene tetratricopeptide repeat domain 28 Neighboring gene small nucleolar RNA SNORD42 Neighboring gene VISTA enhancer hs1645

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_045696.1 

    Range
    101..401
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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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    28056153..28056453 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    28517564..28517864 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)