STCH maps to mouse chromosome 16, extending the conserved synteny with human chromosome 21

Genomics

Volumn 49, Issue 1, 1998, Pages 156-157

  Reeves, Roger H ^a   Rue, Elizabeth ^a   Yu, Jingwei ^b   Kao, Fa Ten ^b  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF DENVER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 16; CHROMOSOME 21; CHROMOSOME ANALYSIS; CHROMOSOME MAP; GENE MAPPING; HUMAN; MOUSE; NONHUMAN; PRIORITY JOURNAL; SYNTENY;

EID: 0032054285     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1998.5215     Document Type: Article

References (7)

1. Brodsky G., Otterson G. A., Parry B. B., Hart I., Patterson D., Kaye F. J. Localization of STCH to human chromosome 21q11.1. Genomics. 30:1995;627-628.
2. Cabin D. E., Hawkins A., Griffin C., Reeves R. H. YAC transgenic mice in the study of the genetic basis of Down syndrome. Progress in Clinical Biology Research. 1994;Wiley-Liss, New York.
3. Cabin D. E., Reeves R. H. Mouse chromosome 16. Mammalian Genome. 7:1997;5264-5273.
4. Otterson G. A., Flynn G. C., Kratzke R. A., Coxon A., Johnston P. G., Kaye F. J. Stch encodes the 'ATPase core' of a microsomal stress 70 protein. EMBO J. 13:1994;1216-1225.
5. Reeves R. H., Irving N. G., Moran T., Wohn A., Kitt C., Sisodia S., Schmidt C., Bronson R. T., Davisson M. T. A mouse model for Down syndrome exhibits learning and behaviour deficits. Nature Genet. 11:1995;177-183.
6. Reeves R. H., Rue E., Citron M., Cabin D. E. High resolution recombinational map of mouse Chromosome 16. Genomics. 1997.
7. Yu J., Tong S., Shen Y., Kao F. T. Gene identification and DNA sequence analysis in the GC-poor 20 megabase region of human chromosome 21. Proc. Natl. Acad. Sci. USA. 94:1997;6862-6867.