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    Cdr1 cerebellar degeneration related antigen 1 [ Mus musculus (house mouse) ]

    Gene ID: 631990, updated on 9-Dec-2024

    Summary

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    Official Symbol
    Cdr1provided by MGI
    Official Full Name
    cerebellar degeneration related antigen 1provided by MGI
    Primary source
    MGI:MGI:88359
    See related
    AllianceGenome:MGI:88359
    Gene type
    unknown
    RefSeq status
    MODEL
    Organism
    Mus musculus
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
    Also known as
    Cdr; Cdr34; Gm2409; Gm7077; EG631990; 100039759
    Summary
    Orthologous to human CDR1 (cerebellar degeneration related 1). [provided by Alliance of Genome Resources, Dec 2024]

    Genomic context

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    See Cdr1 in Genome Data Viewer
    Location:
    X A6; X 34.33 cM
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_02 current GRCm39 (GCF_000001635.27) X NC_000086.8 (60226838..60239449, complement)
    108.20200622 previous assembly GRCm38.p6 (GCF_000001635.26) X NC_000086.7 (61183246..61185558, complement)

    Chromosome X - NC_000086.8Genomic Context describing neighboring genes Neighboring gene predicted gene 14664 Neighboring gene estrogen related receptor, beta pseudogene Neighboring gene cerebellar degeneration related antigen 1, opposite strand Neighboring gene predicted gene 4988 Neighboring gene STARR-seq mESC enhancer starr_47247 Neighboring gene NudC domain containing 2 pseudogene

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. Cerebellar degeneration-related antigen: a highly conserved neuroectodermal marker mapped to chromosomes X in human and mouse. Chen YT, et al. Proc Natl Acad Sci U S A, 1990 Apr. PMID 2326268, Free PMC Article
    2. Distinct roles of prostaglandin H synthases 1 and 2 in T-cell development. Rocca B, et al. J Clin Invest, 1999 May 15. PMID 10330429, Free PMC Article
    3. The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGF beta superfamily. Kingsley DM, et al. Cell, 1992 Oct 30. PMID 1339316
    4. Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome. Quaderi NA, et al. Genomics, 1994 Aug. PMID 8001979
    5. Mapping of FMR1, the gene implicated in fragile X-linked mental retardation, on the mouse X chromosome. Laval SH, et al. Genomics, 1992 Apr. PMID 1572655

    See all (10) citations in PubMed

    GeneRIFs: Gene References Into Functions

    General gene information

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    Markers

    Gene Ontology Provided by MGI

    Function Evidence Code Pubs
    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
    		  
    Component Evidence Code Pubs
    is_active_in cellular_component ND
    No biological Data available
    more info
    		  

    NCBI Reference Sequences (RefSeq)

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    NEW Try the new Transcript table

    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_000086.8 Reference GRCm39 C57BL/6J

      Range
      60226838..60239449 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RNA

    1. XR_008604652.1 RNA Sequence

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_001166658.1: Suppressed sequence

      Description
      NM_001166658.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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