Entry - 602197 - CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 - OMIM

 
 
602197

CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3


Alternative titles; symbols

CDR3


Cytogenetic location: 17q25     Genomic coordinates (GRCh38): 17:72,900,001-83,257,441


▼ TEXT

Fletcher et al. (1997) mapped to mouse chromosome 11 a leucine zipper protein gene (Cdr3) that shows considerable homology to cerebellar degeneration-related autoantigen-2 (CDR2; 117340). From the location of the Cdr3 gene on chromosome 11, the homologous human gene, CDR3, was predicted to be located on 17q25.


▼ REFERENCES

  1. Fletcher, C. F., Okano, H. J., Gilbert, D. J., Yang, Y., Yang, C., Copeland, N. G., Jenkins, N. A., Darnell, R. B. Mouse chromosomal locations of nine genes encoding homologs of human paraneoplastic neurologic disorder antigens. Genomics 45: 313-319, 1997. [PubMed: 9344654, related citations] [Full Text]


Creation Date:
Victor A. McKusick : 12/17/1997
Edit History:
carol : 12/26/2002
carol : 7/6/1998
mark : 12/17/1997
mark : 12/17/1997

602197

CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3


Alternative titles; symbols

CDR3


Cytogenetic location: 17q25     Genomic coordinates (GRCh38): 17:72,900,001-83,257,441


TEXT

Fletcher et al. (1997) mapped to mouse chromosome 11 a leucine zipper protein gene (Cdr3) that shows considerable homology to cerebellar degeneration-related autoantigen-2 (CDR2; 117340). From the location of the Cdr3 gene on chromosome 11, the homologous human gene, CDR3, was predicted to be located on 17q25.


REFERENCES

  1. Fletcher, C. F., Okano, H. J., Gilbert, D. J., Yang, Y., Yang, C., Copeland, N. G., Jenkins, N. A., Darnell, R. B. Mouse chromosomal locations of nine genes encoding homologs of human paraneoplastic neurologic disorder antigens. Genomics 45: 313-319, 1997. [PubMed: 9344654] [Full Text: https://doi.org/10.1006/geno.1997.4925]


Creation Date:
Victor A. McKusick : 12/17/1997

Edit History:
carol : 12/26/2002
carol : 7/6/1998
mark : 12/17/1997
mark : 12/17/1997



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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: May 3, 2024