Mapping Data Summary

• Symbol: Wnt8b
• Name: wingless-type MMTV integration site family, member 8B
• ID: MGI:109485
• Chromosome: 19

7 mapping experiments

Experiment Type	Details	Chromosome	Reference
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
TEXT-Genetic Cross		19	J:51115 Hansen GM, et al., A mouse chromosome 19 genetic map including the Lvis1 viral insertion site. Genomics. 1999 Mar 1;56(2):228-31
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:54055 Ji W, et al., Identification of genes within the Krd deletion on mouse chromosome 19. Mamm Genome. 1999 Apr;10(4):399-401
TEXT-Genetic Cross		19	J:56862 Richardson M, et al., Mouse Wnt8B is expressed in the developing forebrain and maps to chromosome 19. Mamm Genome. 1999 Sep;10(9):923-5
TEXT-Physical Mapping		19	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