30 phenotypes from 3 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tmem30atm1.1Xjz/Tmem30atm1.1Xjz Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6J * DBA	abnormal liver morphology	J:249038
	abnormal spine curvature	J:249038
	bile duct proliferation	J:249038
	cachexia	J:249038
	decreased liver weight	J:249038
	normal growth/size/body region phenotype	J:249038
	normal homeostasis/metabolism phenotype	J:249038
	increased alkaline phosphatase activity	J:249038
	increased bile salt level	J:249038
	increased circulating alanine transaminase level	J:249038
	increased circulating aspartate transaminase level	J:249038
	increased circulating bilirubin level	J:249038
	intrahepatic cholestasis	J:249038
	jaundice	J:249038
	liver fibrosis	J:249038
	liver inflammation	J:249038
	slow movement	J:249038
Tmem30atm1.1Xjz/Tmem30atm1.1Xjz Tg(CAG-cre/Esr1*)5Amc/0 involves: 129/SvEv * C57BL/6 * CBA	abnormal cone electrophysiology	J:253580
	absent photoreceptor outer segment	J:253580
	decreased retina ganglion cell number	J:253580
	photoreceptor outer segment degeneration	J:253580
	short photoreceptor outer segment	J:253580
	thin retina outer nuclear layer	J:253580
Tmem30atm1.1Xjz/Tmem30atm1.1Xjz Tg(Nes-cre)1Kln/0 involves: 129/SvEv * C57BL/6 * SJL	embryonic lethality, complete penetrance	J:253580
Tmem30atm1.1Xjz/Tmem30atm1.1Xjz Tg(OPN1LW-cre)4Yzl/0 involves: 129/SvEv * C57BL/6J * FVB/N	abnormal cone electrophysiology	J:253580
	abnormal retina cone cell morphology	J:253580
	absent retina cone cells	J:253580
	retina cone cell degeneration	J:253580
Tmem30atm1.1Xjz/Tmem30atm1.1Xjz Tg(Six3-cre)69Frty/0 involves: 129/SvEv * C57BL/6 * DBA/2	absent retina	J:253580
	retina degeneration	J:253580
Tmem30atm1a(KOMP)Wtsi/Tmem30atm1a(KOMP)Wtsi C57BL/6N-Tmem30atm1a(KOMP)Wtsi/Wtsi	preweaning lethality, complete penetrance	J:211773
Tmem30atm1Xjz/Tmem30atm1Xjz involves: 129/SvEv	embryonic lethality, complete penetrance	J:253580