53 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Ext2tm1Werb/Ext2+ Sulf2Gt(XST155)Byg/Sulf2Gt(XST155)Byg involves: 129P2/OlaHsd * C57BL/6	prenatal lethality, incomplete penetrance	J:117689
Shhtm1Chg/Shh+ Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10	abnormal craniofacial morphology	J:130163
	absent mandible	J:130163
	anophthalmia	J:130163
	microphthalmia	J:130163
	short mandible	J:130163
Sulf1Gt(OST352220)Lex/Sulf1Gt(OST352220)Lex Sulf2Gt(OST311938)Lex/Sulf2Gt(OST311938)Lex involves: 129S5/SvEvBrd * C57BL/6N	abnormal basisphenoid bone morphology	J:129305
	abnormal sternebra morphology	J:129305
	decreased body length	J:129305
	decreased body weight	J:129305
	decreased bone volume	J:129305
	decreased chondrocyte number	J:129305
	decreased survivor rate	J:129305
	neonatal lethality, incomplete penetrance	J:129305
	postnatal lethality	J:129305
	premature death	J:129305
	small kidney	J:129305
	sternebra fusion	J:129305
Sulf1Gt(XM190)Byg/Sulf1+ Sulf2Gt(PST111)Byg/Sulf2+ involves: 129P2/OlaHsd * C57BL/6	split vertebrae	J:130163
	sternebra fusion	J:130163
Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg involves: 129P2/OlaHsd * C57BL/6	abnormal basisphenoid bone morphology	J:130163
	abnormal cervical axis morphology	J:130163
	abnormal long bone epiphyseal plate proliferative zone	J:130163
	abnormal mandible morphology	J:130163
	abnormal skeleton morphology	J:130163
	abnormal sternum morphology	J:130163
	abnormal vertebral column morphology	J:130163
	caudal vertebral fusion	J:130163
	cervical vertebral transformation	J:130163
	decreased body size	J:130163
	decreased body weight	J:130163
	kinked tail	J:130163
	long incisors	J:130163
	lumbar vertebral fusion	J:130163
	misaligned incisors	J:130163
	premature death	J:130163
	sacral vertebral fusion	J:130163
	short radius	J:130163
	short sternum	J:130163
	small thoracic cage	J:130163
	split vertebrae	J:130163
	sternebra fusion	J:130163
	wide sternum	J:130163
Sulf1tm1.1Cpe/Sulf1tm1.1Cpe Sulf2tm1.1Cpe/Sulf2tm1.1Cpe involves: 129S/SvEv * C57BL/6	abnormal digestive system physiology	J:124898
	abnormal enteric nervous system morphology	J:124898
	abnormal enteric neuron morphology	J:124898
	coughing	J:124898
	decreased body size	J:124898
	dilated esophagus	J:124898
	enlarged esophagus	J:124898
	impaired smooth muscle contractility	J:124898
	postnatal growth retardation	J:124898
	postnatal lethality, incomplete penetrance	J:124898
	reduced fertility	J:124898
	respiratory distress	J:124898
Sulf1tm1Clrm/Sulf1tm1Clrm Sulf2tm1Clrm/Sulf2tm1Clrm involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	abnormal basisphenoid bone morphology	J:130163
	abnormal cervical vertebrae morphology	J:130163
	abnormal sternum morphology	J:130163
	abnormal vertebral column morphology	J:130163
	caudal vertebral fusion	J:130163
	lumbar vertebral fusion	J:130163
	sacral vertebral fusion	J:130163
	short radius	J:130163
	short sternum	J:130163
	split vertebrae	J:130163
	sternebra fusion	J:130163
	thoracic vertebral fusion	J:130163
Sulf1tm1Clrm/Sulf1tm1Clrm Sulf2tm1Clrm/Sulf2tm1Clrm involves: 129S2/SvPas * C57BL/6	abnormal cell physiology	J:116527
	decreased body weight	J:116527
	decreased litter size	J:116527
	premature death	J:116527
Sulf1tm1Mmas/Sulf1tm1Mmas Sulf2tm1Mmas/Sulf2tm1Mmas B6N.129P2-Sulf1tm1Mmas Sulf2tm1Mmas	abnormal cell morphology	J:183277