151 phenotypes from 10 alleles in 12 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf9Aca12/Fgf9+ involves: C57BL/6J	abnormal vision	J:176356
	increased eye anterior chamber depth	J:176356
	small lens	J:176356
	normal vision/eye phenotype	J:176356
Fgf9Aca12/Fgf9Aca12 involves: C57BL/6J	abnormal lens development	J:176356
	abnormal vision	J:176356
	cataract	J:176356
	increased eye anterior chamber depth	J:176356
	normal mortality/aging	J:176356
	normal reproductive system phenotype	J:176356
	normal skeleton phenotype	J:176356
	small lens	J:176356
	normal vision/eye phenotype	J:176356
Fgf9Eks/Fgf9+ involves: C57BL/6J * DBA/2J	fused joints	J:77537
	kinked tail	J:77537
	lethality at weaning, incomplete penetrance	J:77537
	postnatal growth retardation	J:77537
	synostosis	J:146802
Fgf9Eks/Fgf9Eks involves: C57BL/6J * DBA/2J	abnormal cochlea morphology	J:77537
	abnormal humerus morphology	J:77537
	abnormal joint morphology	J:77537
	abnormal long bone morphology	J:77537
	abnormal lung morphology	J:77537
	abnormal radius morphology	J:77537
	abnormal sternum morphology	J:77537
	abnormal temporal bone morphology	J:77537
	abnormal tympanic ring morphology	J:77537
	abnormal vertebral arch morphology	J:77537
	abnormal voluntary movement	J:77537
	cleft secondary palate	J:77537
	cyanosis	J:77537
	enlarged Meckel's cartilage	J:77537
	exophthalmos	J:77537
	fusion of vertebral arches	J:77537
	high forehead	J:77537
	hypopnea	J:77537
	increased diameter of femur	J:77537
	increased diameter of fibula	J:77537
	increased diameter of humerus	J:77537
	increased diameter of radius	J:77537
	increased diameter of tibia	J:77537
	increased diameter of ulna	J:77537
	midface hypoplasia	J:77537
	neonatal lethality, complete penetrance	J:77537
	ocular hypertelorism	J:77537
	premature coronal suture closure	J:77537, J:146802
	premature sagittal suture closure	J:77537
	short femur	J:77537
	short fibula	J:77537
	short humerus	J:77537
	short limbs	J:77537
	short nasal bone	J:77537
	short premaxilla	J:77537
	short radius	J:77537
	short sternum	J:77537
	short tail	J:77537
	short tibia	J:77537
	short ulna	J:77537
	small lung	J:77537
	synostosis	J:77537, J:146802
	wide ribs	J:77537
Fgf9Eks/Fgf9tm1Dor involves: 129S6/SvEvTac * C57BL/6J * DBA/2J	synostosis	J:146802
Fgf9tm1.1Fwan/Fgf9tm1.1Fwan involves: 129S4/SvJaeSor * C57BL/6	no abnormal phenotype detected	J:106766
Fgf9tm1.2Fwan/Fgf9tm1.2Fwan involves: 129S4/SvJaeSor * C57BL/6	pallor	J:106766
	perinatal lethality, complete penetrance	J:106766
	pulmonary hypoplasia	J:106766
	respiratory distress	J:106766
	small lung	J:106766
Fgf9tm1.2Zqch/Fgf9+ involves: 129S6/SvEvTac * C57BL/6J * FVB	abnormal secondary palate development	J:306390
	delayed palatal shelf elevation	J:306390
	small mandible	J:306390
Fgf9tm1.2Zqch/Fgf9tm1.2Zqch involves: 129S6/SvEvTac * C57BL/6J * FVB	abnormal cartilage physiology	J:306390
	abnormal occipital bone morphology	J:306390
	abnormal palatal mesenchymal cell proliferation	J:306390
	abnormal palate bone morphology	J:306390
	abnormal premaxilla morphology	J:306390
	abnormal secondary palate development	J:306390
	abnormal secondary palate morphology	J:306390
	abnormal tongue position	J:306390
	cleft secondary palate	J:306390
	decreased hyaluronic acid level	J:306390
	decreased mouth size	J:306390
	decreased palatal shelf size	J:306390
	delayed palatal shelf elevation	J:306390
	increased tongue size	J:306390
	narrow head	J:306390
	narrow palate	J:306390
	neonatal lethality, complete penetrance	J:306390
	premature bone ossification	J:306390
	short mandible	J:306390
	small mandible	J:306390
Fgf9tm1b(KOMP)Wtsi/Fgf9+ C57BL/6N-Fgf9tm1b(KOMP)Wtsi/H	abnormal retina vasculature morphology	J:211773
	cataract	J:211773
	enlarged heart	J:211773
	hyperactivity	J:211773
Fgf9tm1b(KOMP)Wtsi/Fgf9+ C57BL/6N-Fgf9tm1b(KOMP)Wtsi/J	increased heart weight	J:211773
	increased startle reflex	J:211773
Fgf9tm1b(KOMP)Wtsi/Fgf9tm1b(KOMP)Wtsi C57BL/6N-Fgf9tm1b(KOMP)Wtsi/H	preweaning lethality, complete penetrance	J:211773
Fgf9tm1b(KOMP)Wtsi/Fgf9tm1b(KOMP)Wtsi C57BL/6N-Fgf9tm1b(KOMP)Wtsi/J	abnormal body wall morphology	J:211773
	abnormal embryo size	J:211773
	cleft palate	J:211773
	preweaning lethality, complete penetrance	J:211773
Fgf9tm1Dor/Fgf9+ involves: 129S6/SvEvTac	synostosis	J:146802
Fgf9tm1Dor/Fgf9tm1Dor involves: 129S6/SvEvTac	abnormal lung-associated mesenchyme development	J:107406
Fgf9tm1Dor/Fgf9tm1Dor involves: 129S6/SvEvTac * C57BL/6	abnormal branching involved in lung morphogenesis	J:69852
	abnormal cecum morphology	J:104353
	abnormal digestive system physiology	J:139005
	abnormal Leydig cell differentiation	J:68379
	abnormal mesenchymal cell proliferation involved in lung development	J:69852
	abnormal primary sex determination	J:68379
	abnormal Sertoli cell development	J:68379
	abnormal small intestine crypts of Lieberkuhn morphology	J:139005
	abnormal small intestine morphology	J:139005
	abnormal testis cord formation	J:68379
	abnormal testis morphology	J:68379
	cleft palate	J:69852
	cyanosis	J:69852
	decreased fetal weight	J:69852
	decreased lung weight	J:69852
	decreased number of peritubular myoid cells	J:68379
	dilated heart atrium	J:69852
	dilated heart ventricle	J:69852
	disorganized testis cords	J:68379
	normal endocrine/exocrine gland phenotype	J:68379
	epididymis hypoplasia	J:68379
	hypoxia	J:69852
	neonatal lethality, complete penetrance	J:69852
	ovotestis	J:68379
	perinatal lethality, complete penetrance	J:68379
	primary sex reversal	J:68379
	pulmonary hypoplasia	J:69852
	respiratory failure	J:69852
	testis hypoplasia	J:68379
Fgf9tm1Dor/Fgf9tm1Dor involves: C57BL/6J	abnormal fetal cardiomyocyte proliferation	J:95803
	abnormal heart development	J:95803
	dilated heart left ventricle	J:95803
	dilated heart right ventricle	J:95803
	heart hypoplasia	J:95803
	increased heart atrium size	J:95803
Fgf9tm1Fwan/Fgf9tm1Fwan involves: 129S4/SvJaeSor * C57BL/6	postnatal lethality, incomplete penetrance	J:106766
Fgf9tm1Zgwg/Fgf9+ involves: 129S1/Sv	abnormal coccyx morphology	J:241783
	abnormal incisor morphology	J:241783
	abnormal intervertebral disk morphology	J:241783
	abnormal joint morphology	J:241783
	abnormal tooth development	J:241783
	abnormal voluntary movement	J:241783
	curly tail	J:241783
	fused joints	J:241783
	increased bone ossification	J:241783
	misaligned incisors	J:241783
	synostosis	J:241783
	vertebral fusion	J:241783
Fgf9tm1Zgwg/Fgf9tm1Zgwg involves: 129S1/Sv	abnormal cartilage development	J:241783
	abnormal joint morphology	J:241783
	abnormal knee joint morphology	J:241783
	abnormal limb development	J:241783
	abnormal suckling behavior	J:241783
	abnormal testis morphology	J:241783
	abnormal voluntary movement	J:241783
	calcified joint	J:241783
	caudal vertebral fusion	J:241783
	curly tail	J:241783
	delayed bone ossification	J:241783
	fused joints	J:241783
	increased bone ossification	J:241783
	increased chondrocyte number	J:241783
	postnatal lethality	J:241783
	normal renal/urinary system phenotype	J:241783
	normal respiratory system phenotype	J:241783
	synostosis	J:241783
Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-Fgf9,-EGFP)#Dor/0 involves: FVB	abnormal branching involved in lung morphogenesis	J:224791
	abnormal lung epithelium morphology	J:224791
	abnormal lung-associated mesenchyme development	J:224791
	ascites	J:204282
	increased blastoma incidence	J:224791
	increased lung adenocarcinoma incidence	J:204282
	increased lung adenoma incidence	J:204282
	increased lung tumor incidence	J:204282
	increased malignant tumor incidence	J:204282
	increased mesenchymal cell proliferation involved in lung development	J:224791
	premature death	J:204282
	respiratory failure	J:204282
Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-Fgf9,-EGFP)#Dor/0 Not Specified	abnormal branching involved in lung morphogenesis	J:107406
	abnormal lung development	J:107406
	abnormal lung epithelium morphology	J:107406
	abnormal lung vasculature morphology	J:107406
	abnormal lung-associated mesenchyme development	J:107406
	enlarged lung	J:107406