Symbol Name ID Chromosome |
Col1a2
collagen, type I, alpha 2 MGI:88468 6 |
Experiment Type | Details | Chromosome | Reference |
---|---|---|---|
CROSS |
Cross Type: Backcross |
6 | J:14463 Bahary N, et al., Microdissection of proximal mouse chromosome 6: identification of RFLPs tightly linked to the ob mutation. Mamm Genome. 1993 Sep;4(9):511-5 |
CROSS |
Cross Type: Backcross |
6 | J:3321 Bahary N, et al., Molecular genetic linkage maps of mouse chromosomes 4 and 6. Genomics. 1991 Sep;11(1):33-47 |
CROSS |
Cross Type: Backcross |
6 | J:4348 Chipman SD, et al., Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1701-5 |
CROSS |
Cross Type: Backcross |
6 | J:4348 Chipman SD, et al., Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1701-5 |
CROSS |
Cross Type: Intercross |
6 | J:4348 Chipman SD, et al., Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1701-5 |
CROSS |
Cross Type: Backcross |
6 | J:4348 Chipman SD, et al., Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1701-5 |
CROSS |
Cross Type: Backcross |
6 | J:1908 Friedman JM, et al., Molecular mapping of the mouse ob mutation. Genomics. 1991 Dec;11(4):1054-62 |
CROSS |
Cross Type: Backcross |
6 | J:9991 Irving NG, et al., The alpha 2 chain of type 1 collagen does not map to mouse chromosome 16 but maps close to the Met proto-oncogene on mouse chromosome 6. Cytogenet Cell Genet. 1989;50(2-3):121-2 |
CROSS |
Cross Type: Backcross Mapping Panel: JAX Mouse Mutant Resource BCB |
6 | J:21510 Johnson KR, et al., Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse. Mamm Genome. 1994 Nov;5(11):670-87 |
CROSS |
Cross Type: Backcross |
6 | J:16150 Klocke R, et al., Chromosomal mapping in the mouse of eight K(+)-channel genes representing the four Shaker-like subfamilies Shaker, Shab, Shaw, and Shal. Genomics. 1993 Dec;18(3):568-74 |
CROSS |
Cross Type: Backcross |
6 | J:3210 Siegel D, et al., Localization of the cystic fibrosis transmembrane conductance regulator (Cftr) to mouse chromosome 6. Cytogenet Cell Genet. 1992;61(3):184-5 |
CROSS |
Cross Type: Backcross |
6 | J:752 Steinmeyer K, et al., Inactivation of muscle chloride channel by transposon insertion in myotonic mice. Nature. 1991 Nov 28;354(6351):304-8 |
CROSS |
Cross Type: Backcross |
6 | J:22806 Yen CH, et al., A genomic clone containing a telomere array maps near the centromere of mouse chromosome 6. Mamm Genome. 1995 Feb;6(2):96-102 |
HYBRID | 6 | J:10020 Sundaresan S, et al., Gene for alpha 2(I) collagen is on mouse chromosome 6 not 16. Somat Cell Mol Genet. 1989 Sep;15(5):471-3 | |
TEXT | 6 | J:84436 Ono R, et al., Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6. Genome Res. 2003 Jul;13(7):1696-705 | |
TEXT-Cytogenetic Localization | 6 | J:12366 Naylor SL, et al., The genes for mouse plasminogen activator and urokinase map to Chromosomes 8 and 14, respectively. Cytogenet Cell Genet. 1987;46:669 (Abstr.) | |
TEXT-Genetic Cross | 6 | J:47292 Bronson RT, et al., Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9. Am J Med Genet. 1998 May 26;77(4):289-97 | |
TEXT-Genetic Cross | 6 | J:3210 Siegel D, et al., Localization of the cystic fibrosis transmembrane conductance regulator (Cftr) to mouse chromosome 6. Cytogenet Cell Genet. 1992;61(3):184-5 | |
TEXT-Physical Mapping | 6 | J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573 | |
TEXT-QTL | 6 | J:32894 Primo-Parmo SL, et al., The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family. Genomics. 1996 May 1;33(3):498-507 | |
TEXT-Radiation Hybrid | 6 | 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 12/10/2024 MGI 6.24 |
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