47 phenotypes from 8 alleles in 11 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Sox18Mhdadcc1/Sox18+ C3HeB/FeJ-Sox18Mhdadcc1/Ieg	darkened coat color	J:81301
Sox18Mhdadcc1/Sox18Mhdadcc1 C3HeB/FeJ-Sox18Mhdadcc1/Ieg	abnormal hair growth	J:81301
	darkened coat color	J:81301
	sparse hair	J:81301
Sox18Ra-J/Sox18+ involves: C3H/HeSnJ	darkened coat color	J:30359
	retarded hair growth	J:30359
	short vibrissae	J:30359
	sparse hair	J:30359
Sox18Ra-J/Sox18Ra-J involves: C3H/HeSnJ	abnormal vibrissa number	J:30359
	decreased body size	J:30359
	hairless	J:30359
	neonatal lethality, incomplete penetrance	J:30359
Sox18Ra-Op/Sox18+ involves: C57BL/6J * DBA/2J	abnormal awl hair morphology	J:260
	abnormal hair follicle morphology	J:279
	abnormal hair growth	J:260, J:279
	abnormal vibrissa morphology	J:279
	abnormal vibrissa number	J:260
	abnormal zigzag hair morphology	J:279
	absent auchene hairs	J:260
	cyanosis	J:260
	decreased body size	J:260, J:279
	decreased zigzag hair amount	J:260, J:279
	delayed hair appearance	J:260, J:279
	distended abdomen	J:279
	edema	J:260, J:279
	perinatal lethality, incomplete penetrance	J:260, J:279
	postnatal lethality, incomplete penetrance	J:260, J:279
	short vibrissae	J:279
	skin edema	J:260
	sparse hair	J:260, J:279
Sox18Ra-Op/Sox18Ra-Op B6D2-Sox18Ra-Op/J	abnormal blood vessel morphology	J:150211
	abnormal lymphatic vessel morphology	J:143564
	abnormal pericyte morphology	J:150211
	abnormal vascular endothelial cell physiology	J:150211
	normal cardiovascular system phenotype	J:150211
	edema	J:150211
	hematoma	J:150211
	hemorrhage	J:150211
	increased vascular endothelial cell number	J:150211
	lethality throughout fetal growth and development, complete penetrance	J:143564, J:150211
	skin edema	J:143564, J:150211
Sox18Ra-Op/Sox18Ra-Op involves: C57BL/6J * DBA/2J	embryonic lethality, complete penetrance	J:279
	preweaning lethality, complete penetrance	J:260
Sox18Ra/Sox18+ involves: AG/Cam	chylous ascites	J:6220, J:13089
	decreased total body fat amount	J:13089
	intestinal fibrosis	J:13089
	retarded hair growth	J:13089
Sox18Ra/Sox18+ Not Specified	abnormal hair follicle morphology	J:12991
	abnormal zigzag hair morphology	J:86
	absent auchene hairs	J:86
	chylous ascites	J:13089
	darkened coat color	J:86
	retarded hair growth	J:86
	sparse hair	J:86
Sox18Ra/Sox18Ra Not Specified	alopecia	J:86
	edema	J:86
	preweaning lethality, incomplete penetrance	J:86
Sox18Ragl/Sox18+ involves: 129P3/J * C57BL/6J	chylous ascites	J:83731
	disheveled coat	J:83731
	edema	J:83731
	sparse hair	J:83731
Sox18Ragl/Sox18Ragl involves: 129P3/J * C57BL/6J	chylous ascites	J:83731
	edema	J:83731
	embryonic lethality, incomplete penetrance	J:83731
	hairless	J:83731
	neonatal lethality, complete penetrance	J:83731
Sox18tm1(GFP/cre/ERT2)Pzg/Sox18+ involves: 129S7/SvEvBrd * C57BL/6J	no abnormal phenotype detected	J:159099
Sox18tm1.1(KOMP)Vlcg/Sox18tm1.1(KOMP)Vlcg C57BL/6N-Sox18tm1.1(KOMP)Vlcg/J	abnormal behavior	J:211773
	decreased thigmotaxis	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased circulating sodium level	J:211773
	increased mean corpuscular hemoglobin	J:211773
Sox18tm1Koop/Sox18+ B6.129-Sox18tm1Koop	skin edema	J:143564
Sox18tm1Koop/Sox18tm1Koop B6.129-Sox18tm1Koop	abnormal lymphatic vessel morphology	J:143564
	lethality throughout fetal growth and development, complete penetrance	J:143564
	skin edema	J:143564
Sox18tm1Koop/Sox18tm1Koop involves: 129/Sv * CD-1	abnormal hair growth	J:66010
	darkened coat color	J:66010