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Symbol
Name
ID
Chromosome
Wnt3a
wingless-type MMTV integration site family, member 3A
MGI:98956
11
27 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Backcross
11 J:21916 Ball ST, et al., Mor2, supernatant malate dehydrogenase, is linked to wa2 and Hba on mouse chromosome 11 in a region of homology with human chromosome 2p. Genomics. 1994 Nov 15;24(2):399-400
CROSS Cross Type: Backcross
11 J:21916 Ball ST, et al., Mor2, supernatant malate dehydrogenase, is linked to wa2 and Hba on mouse chromosome 11 in a region of homology with human chromosome 2p. Genomics. 1994 Nov 15;24(2):399-400
CROSS Cross Type: Backcross
11 J:21916 Ball ST, et al., Mor2, supernatant malate dehydrogenase, is linked to wa2 and Hba on mouse chromosome 11 in a region of homology with human chromosome 2p. Genomics. 1994 Nov 15;24(2):399-400
CROSS Cross Type: Backcross
11 J:21916 Ball ST, et al., Mor2, supernatant malate dehydrogenase, is linked to wa2 and Hba on mouse chromosome 11 in a region of homology with human chromosome 2p. Genomics. 1994 Nov 15;24(2):399-400
CROSS Cross Type: Backcross
11 J:31335 Greco TL, et al., Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development. Genes Dev. 1996 Feb 1;10(3):313-24
CROSS Cross Type: Intercross
11 J:7222 Henry EW, et al., Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination. J Neuropathol Exp Neurol. 1983 Nov;42(6):688-706
CROSS Cross Type: Backcross
11 J:7222 Henry EW, et al., Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination. J Neuropathol Exp Neurol. 1983 Nov;42(6):688-706
CROSS Cross Type: Backcross
11 J:7222 Henry EW, et al., Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination. J Neuropathol Exp Neurol. 1983 Nov;42(6):688-706
CROSS Cross Type: Intercross
11 J:9027 Lane PW, et al., Spasmodic, a mutation on chromosome 11 in the mouse. J Hered. 1987 Nov-Dec;78(6):353-6
CROSS Cross Type: Backcross
11 J:9027 Lane PW, et al., Spasmodic, a mutation on chromosome 11 in the mouse. J Hered. 1987 Nov-Dec;78(6):353-6
CROSS Cross Type: Intercross
11 J:9027 Lane PW, et al., Spasmodic, a mutation on chromosome 11 in the mouse. J Hered. 1987 Nov-Dec;78(6):353-6
CROSS Cross Type: Backcross
11 J:14080 Lyon MF, et al., Gene order of Chy-vt-Re on Chromosome 11. Mouse News Lett. 1986;74:96
CROSS Cross Type: Backcross
11 J:14080 Lyon MF, et al., Gene order of Chy-vt-Re on Chromosome 11. Mouse News Lett. 1986;74:96
CROSS Cross Type: Backcross
11 J:28463 MICHIE D, A new linkage in the house mouse; vestigial and Rex. Nature. 1952 Oct 4;170(4327):585-6
CROSS Cross Type: Backcross
11 J:28463 MICHIE D, A new linkage in the house mouse; vestigial and Rex. Nature. 1952 Oct 4;170(4327):585-6
CROSS Cross Type: Backcross
11 J:28463 MICHIE D, A new linkage in the house mouse; vestigial and Rex. Nature. 1952 Oct 4;170(4327):585-6
CROSS Cross Type: Backcross
11 J:28463 MICHIE D, A new linkage in the house mouse; vestigial and Rex. Nature. 1952 Oct 4;170(4327):585-6
CROSS Cross Type: Backcross
11 J:37827 Watkins-Chow DE, et al., Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5. Genomics. 1997 Feb 15;40(1):114-22
CROSS Cross Type: Backcross
11 J:37827 Watkins-Chow DE, et al., Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5. Genomics. 1997 Feb 15;40(1):114-22
CROSS Cross Type: Backcross
11 J:37827 Watkins-Chow DE, et al., Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5. Genomics. 1997 Feb 15;40(1):114-22
CROSS Cross Type: Backcross
11 J:37827 Watkins-Chow DE, et al., Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5. Genomics. 1997 Feb 15;40(1):114-22
CROSS Cross Type: Intercross
11 J:6896 Weimar WR, et al., Vibrator (vb): a spinocerebellar system degeneration with autosomal recessive inheritance in mice. Brain Res. 1982 Nov 18;251(2):357-64
CROSS Cross Type: Intercross
11 J:6896 Weimar WR, et al., Vibrator (vb): a spinocerebellar system degeneration with autosomal recessive inheritance in mice. Brain Res. 1982 Nov 18;251(2):357-64
TEXT-Genetic Cross 11 J:33550 Greco TL, et al., Dishevelled-2 maps to human chromosome 17 and distal to Wnt3a and vestigial tail (vt) on mouse chromosome 11. Mamm Genome. 1996 Jun;7(6):475-6
TEXT-Genetic Cross 11 J:31335 Greco TL, et al., Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development. Genes Dev. 1996 Feb 1;10(3):313-24
TEXT-Genetic Cross 11 J:31335 Greco TL, et al., Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development. Genes Dev. 1996 Feb 1;10(3):313-24
TEXT-Genetic Cross 11 J:47116 Liang Y, et al., Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2. Am J Hum Genet. 1998 Apr;62(4):904-15

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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory