Mapping Data Summary

• Symbol: Fgd3
• Name: FYVE, RhoGEF and PH domain containing 3
• ID: MGI:1353657
• Chromosome: 13

4 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSB)	13	J:60236 Pasteris NG, et al., Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue. Gene. 2000 Jan 25;242(1-2):237-47
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	13	J:60236 Pasteris NG, et al., Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue. Gene. 2000 Jan 25;242(1-2):237-47
TEXT-Physical Mapping		13	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		13	J:71964 Juriloff DM, et al., Multifactorial genetics of exencephaly in SELH/Bc mice. Teratology. 2001 Oct;64(4):189-200