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

Gene ID: 631990, updated on 26-Sep-2022

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 protein 1). [provided by Alliance of Genome Resources, Apr 2022]
Orthologs
human all

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
109 current GRCm39 (GCF_000001635.27) X NC_000086.8 (60226852..60229164, 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 estrogen related receptor, beta pseudogene Neighboring gene cerebellar degeneration related antigen 1, opposite strand Neighboring gene RIKEN cDNA C030023E24 gene Neighboring gene predicted gene 4988

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

Homology

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: Mus musculus Annotation Release 109 details...Open this link in a new tab

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
    60226852..60229164 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001166658.1 → NP_001160130.1  

    UniProtKB/TrEMBL
    E9Q0B4

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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