Assignment of the human diacylglycerol kinase 4 (DAGK4) gene to chromosome 4p16.3

Genomics

Volumn 33, Issue 1, 1996, Pages 145-146

  Endele, Sabine ^a   Zabel, Bernhard ^a   Winterpacht, Andreas ^a  

^a JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACHONDROPLASIA; ARTICLE; CHROMOSOME 4P; GENE ASSIGNMENT; GENE LOCATION; GENETIC SUSCEPTIBILITY; HUMAN; HUNTINGTON CHOREA; INHERITANCE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; WOLF HIRSCHHORN SYNDROME;

EID: 0029944504     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0174     Document Type: Article

References (9)

1. Bucan, M., Zimmer, M., Whaley, W. L., Poustka, A., Youngman, S., Allitto, B. A., Ormondroyd, E., Smith, B., Pohl, T. M., MacDonald, M., Bates, G. P., Richards, J., Volinia, S., Gilliam, T. C., Sedlacek, Z., Collins, F. S., Wasmuth, J. J., Shaw, D. J., Gusella, J. F., Frischauf, A-M., and Lehrach, H. (1990). Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation. Genomics 6: 1-15.
2. Buckler, A. J., Chang, D. D., Graw, S. L., Brook, J. D., Haber, D. A., Sharp, P. A., and Housman, D. E. (1991). Exon amplification: A strategy to isolate mammalian genes based on RNA splicing. Proc. Natl. Acad. Sci. USA 88: 4005-4009.
3. Church, D. M., Stotler, C. J., Rutter, J. L., Murrell, J. R., Trofatter, J. A., and Buckler, A. J. (1994). Isolation of genes from complex sources of mammalian genomic DNA using exon amplification. Nature Genet. 6: 98-105.
4. Gandelmann, K. Y., Gibson, L., Meyn, M. S., and Yang-Feng, T. L. (1992). Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome. Am. J. Hum. Genet. 51: 571-578.
5. Johnson, V. P., Altherr, M. R., Blake, J. M., and Keppen, L. D. (1994). FISH detection of Wolf-Hirschhorn syndrome: Exclusion of D4F26 as critical site. Am. J. Med. Genet. 52: 70-74.
6. Kozak, C. A., and Stephenson, D. A. (1993). Mouse chromosome 5. Mamm. Genome 4: S72-S87.
7. Pilz, A., Schaap, D., Hunt, D., and Fitzgibbon, J. (1995). Chromosomal localization of three mouse diacylglycerol kinase (DAGK) genes: Genes sharing sequence homology to the Drosophila retinal degeneration A (rdgA) gene. Genomics 26: 599-601.
8. Weber, B., Riess, O., Hutchinson, G., Collins, C., Lin, B., Kowbel, D., Andrew, S., Schappert, K., and Hayden, M. R. (1991). Genomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p16.3. Nucleic Acids Res. 19:6263-6268.
9. Whaley, W. L., Bates, G. P., Novelletto, A., Sedlacek, Z., Cheng, S., Romano, D., Ormondroyd, E., Allitto, B., Lin, C., Youngman, S., Baxendale, S., Bucan, M., Altherr, M., Wasmuth, J., Wexler, N. S., Frontali, M., Frischauf, A-M., Lehrach, H., MacDonald, M. E., and Gusella, J. F. (1991). Mapping of cosmid clones in the Huntington's disease region of chromosome 4. Somat. Cell. Mol. Genet. 17: 83-91.