Table 2 |
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|
FGF knockout mice |
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|
Gene |
Survival of null mutant* |
Phenotype |
References |
|
|
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|
Fgf1 |
Viable |
None identified |
[110] |
|
Fgf2 |
Viable |
Mild cardiovascular, skeletal, neuronal |
[110,111,112,113,114] |
|
Fgf3 |
Viable |
Mild inner ear, skeletal (tail) |
[115] |
|
Fgf4 |
Lethal, E4-5 |
Inner cell mass proliferation |
[116] |
|
Fgf5 |
Viable |
Long hair, angora mutation |
[72] |
|
Fgf6 |
Viable |
Subtle, muscle regeneration |
[117,118,119] |
|
Fgf7 |
Viable |
Hair follicle growth, ureteric bud growth |
[120,121] |
|
Fgf8 |
Lethal, E7 |
Gastrulation defect, CNS development, limb development |
[67,70,122,123] |
|
Fgf9 |
Lethal, P0 |
Lung mesenchyme, XY sex reversal |
[124]; (J.S. Colvin et al., personal communication) |
|
Fgf10 |
Lethal, P0 |
Development of multiple organs, including limb, lung, thymus, pituitary |
[125,126,127] |
|
Fgf12 (Fhf1) |
Viable |
Neuromuscular phenotype |
(J. Schoorlemmer and M. Goldfarb, personal communication) |
|
Fgf14 (Fhf4) |
Viable |
Neurological phenotypes |
(Q. Wang, personal communication) |
|
Fgf15 |
Lethal, E9.5 |
Not clear |
(J.R. McWhirter, personal communication) |
|
Fgf17 |
Viable |
Cerebellar development |
[17] |
|
Fgf18 |
Lethal, P0 |
Skeletal development |
(N. Ohbayashi, Z. Liu, personal communication) |
|
|
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*E, embryonic day; P, postnatal day. |
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Ornitz and Itoh Genome Biology 2001 2:reviews3005.1-reviews3005.12 doi:10.1186/gb-2001-2-3-reviews3005 |
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