84 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Sh3pxd2bGt(GST_1527_E5)Lex/Sh3pxd2bGt(GST_1527_E5)Lex involves: 129X1/SvJ * C57BL/6	abnormal basicranium morphology	J:158635
	abnormal cornea morphology	J:158635
	abnormal craniofacial morphology	J:158635
	abnormal heart shape	J:158635
	abnormal heart ventricle morphology	J:158635
	abnormal iliac crest morphology	J:158635
	abnormal ilium wing morphology	J:158635
	abnormal mitral valve morphology	J:158635
	abnormal myocardial trabeculae morphology	J:158635
	abnormal neurocranium morphology	J:158635
	abnormal sagittal suture morphology	J:158635
	abnormal tooth morphology	J:158635
	abnormal xiphoid process morphology	J:158635
	corneal opacity	J:158635
	decreased abdominal adipose tissue amount	J:158635
	decreased body size	J:158635
	decreased heart rate	J:158635
	decreased subcutaneous adipose tissue amount	J:158635
	increased cornea size	J:158635
	increased cornea thickness	J:158635
	kyphosis	J:158635
	lordosis	J:158635
	micrognathia	J:158635
	mitral valve prolapse	J:158635
	ocular hypertelorism	J:158635
	ocular hypertension	J:158635
	phthisis bulbi	J:158635
	postnatal growth retardation	J:158635
	postnatal lethality	J:158635
	short mandible	J:158635
	short maxilla	J:158635
	short nasal bone	J:158635
	thin interventricular septum	J:158635
	Wormian bones	J:158635
Sh3pxd2bnee/Sh3pxd2bnee B10.Cg-H2h4 Sh3pxd2bnee/GrsrJ	abnormal aqueous humor	J:262132
	abnormal eye anterior chamber morphology	J:262132
	abnormal iridocorneal angle	J:262132
	abnormal middle ear morphology	J:153369
	abnormal postnatal growth	J:153369
	abnormal retina morphology	J:262132
	abnormal retina nerve fiber layer morphology	J:262132
	abnormal skeleton development	J:153369
	absent Schlemm's canal	J:262132
	absent trabecular meshwork	J:262132
	anterior iris synechia	J:153369, J:262132
	cataract	J:262132
	corneal opacity	J:153369, J:262132
	corneal vascularization	J:262132
	decreased body size	J:153369, J:262132
	decreased body weight	J:153369
	decreased bone mineral density	J:153369
	decreased cornea thickness	J:262132
	decreased cranium height	J:153369
	decreased total retina thickness	J:262132
	decreased white adipose tissue amount	J:153369
	domed cranium	J:153369
	enlarged eye anterior chamber	J:153369, J:262132
	exophthalmos	J:153369
	eye inflammation	J:262132
	female infertility	J:153369
	gliosis	J:262132
	hyphema	J:262132
	hypopyon	J:262132
	increased eye anterior chamber depth	J:153369, J:262132
	increased or absent threshold for auditory brainstem response	J:153369
	increased susceptibility to otitis media	J:153369
	infertility	J:153369
	irregularly shaped pupil	J:262132
	male infertility	J:153369
	mature cataract	J:262132
	ocular hypertension	J:262132
	optic nerve atrophy	J:262132
	optic nerve cupping	J:262132
	optic nerve degeneration	J:262132
	posterior subcapsular cataract	J:262132
	proportional dwarf	J:153369
	retina ganglion cell degeneration	J:262132
	short snout	J:153369
Sh3pxd2btm1.1Arte/Sh3pxd2btm1.1Arte involves: C57BL/6NTac	abnormal adipose tissue development	J:235640
	abnormal craniofacial morphology	J:235640
	abnormal skeleton development	J:235640
	decreased body fat mass	J:235640
	decreased body size	J:235640
	decreased body weight	J:235640
	decreased gonadal fat pad weight	J:235640
	decreased length of long bones	J:235640
	decreased renal fat pad weight	J:235640
	decreased subcutaneous adipose tissue amount	J:235640
	exophthalmos	J:235640
	infertility	J:235640
	kyphosis	J:235640
	large anterior fontanelle	J:235640
	lipodystrophy	J:235640
	short femur	J:235640
	short tibia	J:235640