A PDZ domain-containing protein with homology to Diphor-1 maps to human chromosome 1q21

Annals of Human Genetics

Volumn 62, Issue 4, 1998, Pages 287-290

  White, K E ^a   Biber, J ^b   Murer, H ^b   Econs, M J ^a  

^a INDIANA UNIVERSITY   (United States)

^b UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; PHOSPHATE;

ANIMAL CELL; ARTICLE; CHROMOSOME 1Q; CONTROLLED STUDY; GENE EXPRESSION; GENE MAPPING; HUMAN; HUMAN CELL; HYPOPHOSPHATEMIA; KIDNEY; NONHUMAN; NUCLEOTIDE SEQUENCE; PHOSPHATE TRANSPORT; PRIORITY JOURNAL; PROTEIN DOMAIN; RICKETS; SEQUENCE HOMOLOGY;

ANIMALS; CARRIER PROTEINS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; DNA, COMPLEMENTARY; HUMANS; KIDNEY; MEMBRANE PROTEINS; RATS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA;

ANIMALIA;

EID: 0032408559     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480098006964     Document Type: Article

References (11)

1. CUSTER, M., SPINDLER, B., VERREY, F., MURER, H. & BIBER, J. (1997). Identification of a new gene product (diphor-1) regulated by dietary phosphate. American Journal of Physiology 273, F801-F806.
2. DRWINGA, H. L., TOJI, L. H., KIM, C. H., GREENE, A. E. & MULIVOR, R. A. (1993). NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2. Genomics 16, 311-314.
3. ECONS, M. J. & MCENERY, P. T. (1997). Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate wasting disorder. J. Clin. Endocrinol. Metab. 82, 674-681.
4. ECONS, M. J., MCENERY, P. T., LENNON, F. & SPEER, M. C. (1997). Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13. J. Clin. Invest. 100, 2653-2657.
5. GAZIT, D., TIEDER, M., LIBERMAN, U. A., PASSI-EVEN, L. & BAB, I. A. (1991). Osteomalacia in hereditary hypophosphatemic rickets with hypercalciuria : a cor-relative clinical-histomorphometric study. Journal of Clinical Endocrinology & Metabolism 72, 229-235.
6. GELB, B. D., SPENCER, E., OBAD, S., et al. (1996). Pyendysostosis : refined linkage and radiation hybrid analyses reduce the critical region to 2 cM at 1q21 and map two candidate genes. Hum. Genet. 98, 141-144.
7. PIZZUTI, A., NOVELLI, G., MARI, A., et al. (1996). Human homolog sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge-syndrome. Hum. Genet. 58, 722-729.
8. POSTING, C. P., PHILLIPS, C., DAVIES, K. E. & BLAKE, D. J. (1997). PDZ domains: targeting signalling molecules to sub-membranous sites. Bioessays 19, 469-479.
9. SHENG, M. & WYSZYNSKI, M. Ion channel targeting in neurons. (1997). Bioessays 19, 847-853.
10. TAKAI, S., KASAMA, M., YAMADA, K., et al. (1994). Human high-affinity FegRI (CD64) gene mapped to chromosome 1q21.2-q21.3 by fluorescence in situ hybridizations. Hum. Genet. 93, 13-15.
11. TASSABEHJI, M., METCALFE, K., FERGUSSON, W. D., et al. (1996). LIM-kinase deleted in Williams syndrome. Nature Genetics 13, 272-273.