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Cwc22rt5 CWC22 spliceosome-associated protein, retrotransposed 5 [ Mus musculus (house mouse) ]

Gene ID: 668113, updated on 2-Nov-2024

Summary

Official Symbol
Cwc22rt5provided by MGI
Official Full Name
CWC22 spliceosome-associated protein, retrotransposed 5provided by MGI
Primary source
MGI:MGI:3702064
See related
Ensembl:ENSMUSG00000096337 AllianceGenome:MGI:3702064
Gene type
pseudo
RefSeq status
INFERRED
Organism
Mus musculus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
Also known as
Gm13694
Summary
Predicted to enable RNA binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in cytosol and nuclear speck. Predicted to be part of U2-type catalytic step 1 spliceosome; U2-type catalytic step 2 spliceosome; and U2-type precatalytic spliceosome. Orthologous to human CWC22 (CWC22 spliceosome associated protein homolog). [provided by Alliance of Genome Resources, Nov 2024]
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Genomic context

See Cwc22rt5 in Genome Data Viewer
Location:
2 D; 2 49.33 cM
Annotation release Status Assembly Chr Location
RS_2024_02 current GRCm39 (GCF_000001635.27) 2 NC_000068.8 (83809189..83812242)
108.20200622 previous assembly GRCm38.p6 (GCF_000001635.26) 2 NC_000068.7 (83978845..83981898)

Chromosome 2 - NC_000068.8Genomic Context describing neighboring genes Neighboring gene CWC22 spliceosome-associated protein, retrotransposed 3 Neighboring gene CWC22 spliceosome-associated protein, retrotransposed 4 Neighboring gene CWC22 spliceosome-associated protein, retrotransposed 7 Neighboring gene CWC22 spliceosome-associated protein, retrotransposed 6 Neighboring gene STARR-positive B cell enhancer mm9_chr2:83833380-83833680

Genomic regions, transcripts, and products

General gene information

Other Names

  • CWC22 spliceosome-associated protein homolog pseudogene

Gene Ontology Provided by MGI

Function Evidence Code Pubs
enables RNA binding ISO
Inferred from Sequence Orthology
more info
 
enables molecular_function ND
No biological Data available
more info
 
Process Evidence Code Pubs
involved_in biological_process ND
No biological Data available
more info
 
involved_in mRNA splicing, via spliceosome ISO
Inferred from Sequence Orthology
more info
 
Component Evidence Code Pubs
part_of U2-type catalytic step 1 spliceosome ISO
Inferred from Sequence Orthology
more info
 
part_of U2-type catalytic step 2 spliceosome ISO
Inferred from Sequence Orthology
more info
 
part_of U2-type precatalytic spliceosome ISO
Inferred from Sequence Orthology
more info
 
part_of catalytic step 2 spliceosome ISO
Inferred from Sequence Orthology
more info
 
is_active_in cellular_component ND
No biological Data available
more info
 
located_in cytosol ISO
Inferred from Sequence Orthology
more info
 
located_in nuclear speck ISO
Inferred from Sequence Orthology
more info
 
located_in nucleus ISO
Inferred from Sequence Orthology
more info
 
part_of spliceosomal complex ISO
Inferred from Sequence Orthology
more info
 

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_029939.1 

    Range
    101..3154
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001635.27-RS_2024_02

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

Reference GRCm39 C57BL/6J

Genomic

  1. NC_000068.8 Reference GRCm39 C57BL/6J

    Range
    83809189..83812242
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001177429.1: Suppressed sequence

    Description
    NM_001177429.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.