Symbol Name ID Chromosome |
D19Mit11.1
DNA segment, Chr 19, Massachusetts Institute of Technology 11.1 MGI:91217 19 |
Experiment Type | Details | Chromosome | Reference |
---|---|---|---|
CROSS |
Cross Type: Backcross |
19 | J:48979 Bloom ML, et al., The hemoglobin-deficit mutation is located on mouse chromosome 19. Mamm Genome. 1998 Aug;9(8):666-7 |
CROSS |
Cross Type: Backcross Mapping Panel: JAX (BSS) |
19 | J:44483 Brady KP, et al., Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis. Genome Res. 1997 Nov;7(11):1085-93 |
CROSS |
Cross Type: Unspecified |
19 | J:37055 Favor J, et al., 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 U S A. 1996 Nov 26;93(24):13870-5 |
CROSS |
Cross Type: Backcross |
19 | J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9 |
CROSS |
Cross Type: Backcross |
19 | J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9 |
CROSS |
Cross Type: Backcross |
19 | J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20 |
CROSS |
Cross Type: Backcross Mapping Panel: JAX (BSS) |
19 | J:42393 Lammert F, et al., The gene encoding the multispecific organic anion transporter of the hepatocyte canalicular membraine (Cmoat) maps to mouse Chromosome 19. Mamm Genome. 1998 Jan;9(1):87-88 |
CROSS |
Cross Type: Backcross |
19 | J:18648 O'Brien EP, et al., Molecular map of chromosome 19 including three genes affecting bleeding time: ep, ru, and bm. Mamm Genome. 1994 Jun;5(6):356-60 |
CROSS |
Cross Type: Backcross |
19 | J:34775 Pretsch W, et al., A precise localization of a mouse gene encoding increased phosphoglycerate mutase activity (Pgam1e1) on Chromosome 19. Mamm Genome. 1996 Aug;7(8):619 |
CROSS |
Cross Type: Intercross |
19 | J:68175 Rieger DK, et al., A double-deletion mutation in the pitx3 gene causes arrested lens development in aphakia mice. Genomics. 2001 Feb 15;72(1):61-72 |
CROSS |
Cross Type: Backcross Mapping Panel: JAX (BSS) |
19 | J:57572 Scott IC, et al., Assignment of TLL1 and TLL2, which encode human BMP-1/Tolloid-related metalloproteases, to chromosomes 4q32-->q33 and 10q23-->q24 and assignment of murine Tll2 to chromosome 19. Cytogenet Cell Genet. 1999;86(1):64-5 |
CROSS |
Cross Type: Backcross Mapping Panel: JAX (BSS) |
19 | J:59226 Suriyapperuma SP, et al., The mouse adducin gene family: alternative splicing and chromosomal localization. Mamm Genome. 2000 Jan;11(1):16-23 |
CROSS |
Cross Type: Backcross Mapping Panel: JAX (BSS) |
19 | J:39608 Wright A, et al., Mart1 is located on mouse chromosome 19 and is excluded as a candidate for ep and ru. Mamm Genome. 1997 May;8(5):377-8 |
CROSS |
Cross Type: Backcross Mapping Panel: JAX (BSS) |
19 | J:43273 Yu YE, et al., Characterization of a transgene-induced mutant mouse line showing thymus atrophy and neuronal degeneration. Mouse Genome. 1997;95(3):704-706 |
RI |
RI/RC Set: AXB |
19 | J:36911 Naggert JK, et al., An additional 136 SSLP markers typed for the AXB and BXA recombinant inbred mouse strains. Mamm Genome. 1997 Mar;8(3):209-11 |
RI |
RI/RC Set: BXA |
19 | J:36911 Naggert JK, et al., An additional 136 SSLP markers typed for the AXB and BXA recombinant inbred mouse strains. Mamm Genome. 1997 Mar;8(3):209-11 |
RI |
RI/RC Set: SMXA |
19 | J:30437 Nishimura M, et al., The SMXA: a new set of recombinant inbred strain of mice consisting of 26 substrains and their genetic profile. Mamm Genome. 1995 Dec;6(12):850-7 |
RI |
RI/RC Set: OcB |
19 | J:31555 Stassen AP, et al., Genetic composition of the recombinant congenic strains. Mamm Genome. 1996 Jan;7(1):55-8 |
RI |
RI/RC Set: CcS |
19 | J:31555 Stassen AP, et al., Genetic composition of the recombinant congenic strains. Mamm Genome. 1996 Jan;7(1):55-8 |
RI |
RI/RC Set: AKXL |
19 | J:28086 Taylor BA, et al., Typing recombinant inbred mouse strains for microsatellite markers on chromosomes 10, 16, 18, 19, and X. Mamm Genome. 1995 Aug;6(8):493-8 |
RI |
RI/RC Set: Not Specified |
19 | J:28086 Taylor BA, et al., Typing recombinant inbred mouse strains for microsatellite markers on chromosomes 10, 16, 18, 19, and X. Mamm Genome. 1995 Aug;6(8):493-8 |
RI |
RI/RC Set: AKXD |
19 | J:28086 Taylor BA, et al., Typing recombinant inbred mouse strains for microsatellite markers on chromosomes 10, 16, 18, 19, and X. Mamm Genome. 1995 Aug;6(8):493-8 |
TEXT | 19 | J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20 | |
TEXT | 19 | J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20 | |
TEXT-Genetic Cross | 19 | J:42484 Gardner JM, et al., The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9238-43 | |
TEXT-Genetic Cross | 19 | J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9 | |
TEXT-Genetic Cross | 19 | J:29220 Johnson KR, et al., Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac. Genomics. 1995 Sep 20;29(2):457-64 | |
TEXT-Genetic Cross | 19 | J:29220 Johnson KR, et al., Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac. Genomics. 1995 Sep 20;29(2):457-64 | |
TEXT-Physical Mapping | 19 | J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006; | |
TEXT-QTL | 19 | J:89309 Korstanje R, et al., Influence of sex and diet on quantitative trait loci for HDL cholesterol levels in an SM/J by NZB/BlNJ intercross population. J Lipid Res. 2004 May;45(5):881-8 | |
TEXT-QTL | 19 | J:55632 Upadhya P, et al., Genetic modifiers of polycystic kidney disease in intersubspecific KAT2J mutants. Genomics. 1999 Jun 1;58(2):129-37 | |
TEXT-QTL | 19 | J:35434 Vyse TJ, et al., Backcross analysis of genes linked to autoantibody production in New Zealand White mice. J Immunol. 1996 Sep 15;157(6):2719-27 | |
TEXT-Radiation Hybrid | 19 | J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004; |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 11/12/2024 MGI 6.24 |
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