44 phenotypes from 6 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tgif1tm1.1Caw/Tgif1+ B6.129S-Tgif1tm1.1Caw	abnormal middle ear morphology	J:198238
	abnormal placenta intervillous maternal lacunae morphology	J:198238
	abnormal placenta labyrinth morphology	J:198238
	hydrocephaly	J:198238
	impaired hearing	J:198238
	increased or absent threshold for auditory brainstem response	J:198238
	increased placenta intervillous maternal lacunae size	J:198238
Tgif1tm1.1Caw/Tgif1tm1.1Caw B6.129S-Tgif1tm1.1Caw	abnormal cytokine level	J:198238
	abnormal fluid regulation	J:198238
	abnormal middle ear morphology	J:198238
	abnormal pinna reflex	J:198238
	abnormal placenta intervillous maternal lacunae morphology	J:198238
	abnormal placenta labyrinth morphology	J:198238
	abnormal pregnancy	J:198238
	conductive hearing loss	J:198238
	deafness	J:198238
	decreased body size	J:198238
	hydrocephaly	J:198238
	impaired hearing	J:198238
	increased middle ear goblet cell number	J:198238
	increased or absent threshold for auditory brainstem response	J:198238
	increased placenta intervillous maternal lacunae size	J:198238
	increased susceptibility to otitis media	J:198238
	middle ear effusion	J:198238
	middle ear polyps	J:198238
	preweaning lethality, incomplete penetrance	J:198238
	reduced female fertility	J:198238
	short face	J:198238
	short nasal bone	J:198238
Tgif1tm1.1Caw/Tgif1tm1.1Caw involves: C57BL/6 * FVB/N	no abnormal phenotype detected	J:97642
Tgif1tm1Caw/Tgif1tm1Caw involves: 129S/SvEv * C57BL/6 * FVB/N	no abnormal phenotype detected	J:97642
Tgif1tm1Dwot/Tgif1+ involves: 129X1/SvJ * C57BL/6J	abnormal response to vitamins	J:105576
	exencephaly	J:105576
Tgif1tm1Dwot/Tgif1tm1Dwot involves: 129X1/SvJ * C57BL/6J	abnormal response to vitamins	J:105576
	exencephaly	J:105576
Tgif1tm1Jxd/Tgif1tm1Jxd either: (involves: 129S/SvEv) or (involves: 129 * C57BL/6)	no abnormal phenotype detected	J:104200
Tgif1tm1Pah/Tgif1tm1Pah B6.129-Tgif1tm1Pah	embryonic growth retardation	J:109616
Tgif1tm1Pah/Tgif1tm1Pah involves: 129S/SvEv * CD-1	abnormal cell cycle	J:109616
	decreased body size	J:109616
	decreased cell proliferation	J:109616
	kinked tail	J:109616
	situs ambiguus	J:109616
	situs inversus	J:109616
Tgif1tm1Ychn/Tgif1+ involves: 129X1/SvJ * C57BL/6	abnormal brain development	J:117761
	abnormal folding of telencephalic vesicles	J:117761
	abnormal forebrain development	J:117761
	abnormal hindbrain development	J:117761
	abnormal midface morphology	J:117761
	abnormal snout morphology	J:117761
	abnormal upper lip morphology	J:117761
	embryonic lethality during organogenesis, incomplete penetrance	J:117761
	exencephaly	J:117761
	holoprosencephaly	J:117761
	microcephaly	J:117761
	philtrum hypoplasia	J:117761
	prenatal lethality, incomplete penetrance	J:117761
	small brain ventricles	J:117761
Tgif1tm1Ychn/Tgif1tm1Ychn involves: 129X1/SvJ * C57BL/6	abnormal brain development	J:117761
	exencephaly	J:117761
	prenatal lethality, incomplete penetrance	J:117761