98 phenotypes from 5 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Crim1em1(IMPC)Wtsi/Crim1+ C57BL/6N-Crim1em1(IMPC)Wtsi/WtsiOrl	trunk curl	J:211773
Crim1em1(IMPC)Wtsi/Crim1em1(IMPC)Wtsi C57BL/6N-Crim1em1(IMPC)Wtsi/WtsiOrl	abnormal ductus venosus valve morphology	J:239583
	abnormal eye morphology	J:239583
	abnormal hepatic portal vein connection	J:239583
	abnormal hypoglossal nerve topology	J:239583
	abnormal Meckel's cartilage morphology	J:239583
	abnormal Mullerian duct topology	J:239583
	abnormal rib morphology	J:239583
	abnormal vertebral arch morphology	J:239583
	abnormal vertebral artery topology	J:239583
	abnormal vitelline vein connection	J:239583
	abnormal vitelline vein topology	J:239583
	absent connection between subcutaneous lymph vessels and lymph sac	J:239583
	absent ductus venosus	J:239583
	absent ductus venosus valve	J:239583
	absent mandibular nerve	J:239583
	absent posterior communicating artery	J:239583
	absent segment of posterior cerebral artery	J:239583
	anal atresia	J:239583
	anastomosis between internal carotid artery and basilar artery	J:239583
	aortic arch coarctation	J:239583
	blood in lymph vessels	J:239583
	decreased parotid gland size	J:239583
	fragmented Meckel's cartilage	J:239583
	fused dorsal root ganglion	J:239583
	fusion of vertebral arches	J:239583
	herniated liver	J:239583
	lens dislocation	J:239583
	muscular ventricular septal defect	J:239583
	perimembraneous ventricular septal defect	J:239583
	preweaning lethality, complete penetrance	J:211773
	pulmonary vein hypoplasia	J:239583
	retrolental blood	J:239583
	subcutaneous edema	J:239583
	syndactyly	J:239583
	telangiectasia	J:239583
Crim1Gt(KST264)Byg/Crim1+ involves: 129P2/OlaHsd * C57BL/6	abnormal glomerular capillary morphology	J:147543
	dilated glomerular capillary	J:147543
	glomerulus hemorrhage	J:147543
Crim1Gt(KST264)Byg/Crim1+ involves: 129P2/OlaHsd * C57BL/6 * CD-1	dilated renal tubule	J:147543
	renal interstitial fibrosis	J:147543
	normal renal/urinary system phenotype	J:147543
Crim1Gt(KST264)Byg/Crim1Gt(KST264)Byg involves: 129P2/OlaHsd * C57BL/6	abnormal eye posterior chamber morphology	J:117237
	abnormal glomerular capillary endothelium morphology	J:147543
	abnormal glomerular capillary morphology	J:147543
	abnormal optic cup morphology	J:117237
	abnormal podocyte foot process morphology	J:147543
	abnormal podocyte morphology	J:147543
	abnormal renal glomerulus basement membrane morphology	J:147543
	cerebral edema	J:117237
	decreased podocyte number	J:147543
	dilated glomerular capillary	J:147543
	fetal bleb	J:117237
	glomerulus hemorrhage	J:147543
	hematoma	J:117237
	increased renal glomerulus basement membrane thickness	J:147543
	mesangiolysis	J:147543
	perinatal lethality, complete penetrance	J:117237
	podocyte foot process effacement	J:147543
	renal glomerulus hypertrophy	J:147543
	small kidney	J:117237
	small lens	J:117237
	syndactyly	J:117237
Crim1Gt(KST264)Byg/Crim1Gt(KST264)Byg involves: 129P2/OlaHsd * C57BL/6 * CD-1	abnormal basal lamina morphology	J:172334
	abnormal glomerular capillary endothelium morphology	J:147543
	abnormal glomerular filtration barrier function	J:172334
	abnormal kidney corticomedullary boundary morphology	J:187026
	abnormal kidney pelvis morphology	J:187026
	abnormal peritubular capillary endothelium morphology	J:172334
	abnormal peritubular capillary morphology	J:172334
	abnormal renal filtration rate	J:187026
	abnormal renal glomerulus morphology	J:172334
	abnormal renin activity	J:172334
	absent glomerular endothelium fenestra	J:147543
	albuminuria	J:147543
	normal cardiovascular system phenotype	J:147543
	cortical renal glomerulopathies	J:147543
	decreased renal glomerular filtration rate	J:147543
	decreased renal glomerulus basement membrane thickness	J:172334
	decreased survivor rate	J:147543
	dilated glomerular capillary	J:172334
	dilated renal tubule	J:147543
	glomerulosclerosis	J:172334
	normal growth/size/body region phenotype	J:147543
	normal hematopoietic system phenotype	J:147543
	hydronephrosis	J:187026
	impaired ureteric peristalsis	J:187026
	increased glomerular capsule space	J:147543
	increased kidney apoptosis	J:187026
	increased vascular permeability	J:172334
	kidney cortex cyst	J:147543, J:187026
	kidney inflammation	J:172334
	kidney papillary atrophy	J:187026
	kidney papillary hypoplasia	J:187026
	perinatal lethality, incomplete penetrance	J:147543
	podocyte foot process effacement	J:147543, J:172334
	renal glomerulus cyst	J:147543, J:172334, J:187026
	renal glomerulus hypertrophy	J:147543
	renal interstitial fibrosis	J:147543, J:172334
	renal tubular necrosis	J:172334
	normal renal/urinary system phenotype	J:147543, J:172334
	short kidney papilla	J:187026
	small kidney	J:187026
Crim1tm1(GFP/cre/ERT2)Pzg/Crim1+ involves: 129S7/SvEvBrd * C57BL/6	no abnormal phenotype detected	J:159099
Crim1tm1.1Dpen/Crim1tm1.1Dpen B6.129P2(129S7)-Crim1tm1.1Dpen	postnatal lethality, complete penetrance	J:187855
Crim1tm1.1Dpen/Crim1tm1.1Dpen either: (B6.129P2(129S7)-Crim1tm1.1Dpen) or (involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CD-1)	abnormal renal glomerulus morphology	J:187855
	bleb	J:187855
	edema	J:187855
	microphthalmia	J:187855
	renal hypoplasia	J:187855
	syndactyly	J:187855
Crim1tm1.1Dpen/Crim1tm1.1Dpen involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CD-1	lethality, incomplete penetrance	J:187855
Crim1tm1Dpen/Crim1tm1Dpen B6.129P2-Crim1tm1Dpen	no abnormal phenotype detected	J:187855
Crim1tm1Dpen/Crim1tm1Dpen involves: 129P2/OlaHsd * C57BL/6 * CD-1	no abnormal phenotype detected	J:187855