Identification of genes within the Krd deletion on mouse chromosome 19

Mammalian Genome

Volumn 10, Issue 4, 1999, Pages 399-401

  Ji, Weizhen ^a   Herron, Bruce ^b   Jones, Julie M ^a   Jenkins, Nancy A ^c   Gilbert, Debra J ^c   Copeland, Neal G ^c   Swank, Richard ^d   Flaherty, Lorraine ^b   Meisler, Miriam H ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b WADSWORTH CENTER   (United States)

^c NATIONAL CANCER INSTITUTE   (United States)

^d ROSWELL PARK CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 19; DNA FLANKING REGION; GENE DELETION; GENE INSERTION; GENETIC ANALYSIS; GENETIC RECOMBINATION; SINGLE STRAND CONFORMATION POLYMORPHISM; TRANSCRIPTION REGULATION;

ANIMALS; CHROMOSOME MAPPING; GENOME; MICE; PROTEINS; SEQUENCE DELETION; WNT PROTEINS;

EID: 0032776610     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359901010     Document Type: Article

References (17)

1. Copeland NG, Jenkins NA (1991) Development and applications of a molecular genetic linkage map of the mouse genome. Trends Genet 7, 113-118
2. Davis AP, Justice MJ (1998) Meeting report: 11th International Mouse Genome Conference. Mamm Genome 9, 345-348
3. Dressler GR (1996) Pax-2, kidney development, and oncogenesis. Med Pediatr Oncol 27, 440-444
4. Favor J, Sandulache R, Neuhauser-Klaus A, Pretsch W, Chatterjee B, et al. (1996) The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney. Proc Natl Acad Sci USA 93, 13870-13875
5. Feng GH, Bailin T, Oh J, Spritz, RA (1997) Mouse pale ear (ep) is homologous to human Hermansky-Pudlak syndrome and contains a rare 'AT-AC' intron. Hum Mol Genet 6, 793-797
6. Gardner JM, Wildenberg SC, Keiper NM, Novak EK, Rusiniak ME, et al. (1997) The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome. Proc Natl Acad Sci USA 94, 9238-9243
7. Huang JD, Cope MJ, Mermall V, Strobel MC, Kendrick-Jones J, et al. (1998a) Molecular genetic dissection of mouse unconventional myosin-VA: head region mutations. Genetics 148, 1951-1961
8. Huang JD, Mermall V, Strobel MC, Russell LB, Mooseker MS, et al. (1998b) Molecular genetic dissection of mouse unconventional myosin-VA: tail region mutations. Genetics 148, 1963-1972
9. Keller SA, Jones JM, Boyle A, Barrow LL, Killen PD, et al. (1994) Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics 23, 309-320
10. Lammert F, Cohen DE, Paigen B, Carey MC, Beier DR (1998) The gene encoding the multispecific organic anion transporter (Cmoat) of the hepatocyte canalicular membrane maps to mouse chromosome 19. Mamm Genome 9, 87-88
11. Nomura H, Turco AE, Pei Y, Kalaydjieva L, Schiavello T, et al. (1998) Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects. J Biol Chem 273, 25967-25973
12. Otteson DC, Shelden E, Jones JM, Kameoka J, Hitchcock PF (1998) Pax2 expression and retinal morphogenesis in the normal and Krd mouse. Dev Biol 193, 209-224
13. Poirier C, Guénet J-L (1997) Mouse Chromosome 19. Mamm Genome 7(Suppl), S305-S312
14. Sanyanusin P, Schimmenti LA, McNoe LA, Ward TA, Pierpont MEM, et al. (1995) Mutation of the PAX2 gene in family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. Nat Genet 9, 358-364
15. Schimenti LA, Cunliffe HE, McNoe LA, Ward TA, French MC, et al. (1997) Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations. Am J Hum Genet 60, 869-878
16. Semina EV, Reiter RS, Murray JC (1997) Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19. Hum Mol Genet 6, 2109-2116
17. Semina EV, Ferrell RE, Mintz-Hittner HA, Bitoun P, Alward WLM, et al. (1998) A novel homeobox gene PITX3 is mutated in families with autosomal dominant cataracts and ASMD. Nat Genet 19, 167-170