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RN7SL263P RNA, 7SL, cytoplasmic 263, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480993, updated on 13-May-2022

Summary

Official Symbol
RN7SL263Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 263, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46279
See related
Ensembl:ENSG00000240160 AllianceGenome:HGNC:46279
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
BCR; rbc
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Genomic context

See RN7SL263P in Genome Data Viewer
Location:
22q11.23
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (23261782..23262061, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (23684661..23684940, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (23603969..23604248, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene radial spoke head 14 homolog Neighboring gene BCR pseudogene 8 Neighboring gene BCR activator of RhoGEF and GTPase Neighboring gene BCR-ABL minor-breakpoint cluster region Neighboring gene Sharpr-MPRA regulatory region 5876 Neighboring gene BCR-ABL p195 breakpoint cluster region Neighboring gene F-box and WD repeat domain containing 4 pseudogene 1

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_045086.1 

    Range
    101..380
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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
    23261782..23262061 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    23684661..23684940 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)