49 phenotypes from 7 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Grhl2clft3/Grhl2clft3 involves: A/J * FVB/N	decreased brain size	J:174027
	encephalomeningocele	J:174027
	midline facial cleft	J:174027
Grhl2em1(IMPC)Mbp/Grhl2+ C57BL/6N-Grhl2em1(IMPC)Mbp/MbpMmucd	abnormal blood vessel morphology	J:211773
	abnormal placenta morphology	J:211773
	increased freezing behavior	J:211773
	increased startle reflex	J:211773
Grhl2em1(IMPC)Mbp/Grhl2em1(IMPC)Mbp C57BL/6N-Grhl2em1(IMPC)Mbp/MbpMmucd	abnormal abdominal wall morphology	J:211773
	abnormal craniofacial morphology	J:211773
	abnormal forebrain development	J:211773
	abnormal head shape	J:211773
	abnormal heart morphology	J:211773
	abnormal hindbrain development	J:211773
	abnormal limb morphology	J:211773
	abnormal midbrain development	J:211773
	abnormal neural tube closure	J:211773
	abnormal neural tube morphology	J:211773
	abnormal optic vesicle formation	J:211773
	abnormal pericardium morphology	J:211773
	embryonic growth retardation	J:211773
	exencephaly	J:211773
	preweaning lethality, complete penetrance	J:211773
	syndactyly	J:211773
Grhl2Gt(AC0205)Wtsi/Grhl2+ involves: 129P2/OlaHsd * C57BL/6	exencephaly	J:170759
	facial cleft	J:170759
	incomplete rostral neuropore closure	J:170759
Grhl2Gt(AC0205)Wtsi/Grhl2Gt(AC0205)Wtsi involves: 129P2/OlaHsd * BALB/c * C57BL/6	abnormal neural tube closure	J:170759
	embryonic lethality during organogenesis, complete penetrance	J:170759
	exencephaly	J:170759
	facial cleft	J:170759
	incomplete rostral neuropore closure	J:170759
	spina bifida	J:170759
Grhl2Gt(AC0205)Wtsi/Grhl2Gt(AC0205)Wtsi involves: 129P2/OlaHsd * C57BL/6	embryonic lethality during organogenesis, complete penetrance	J:170759
Grhl2Gt(E115B04)Wrst/Grhl2Gt(E115B04)Wrst involves: 129P2/OlaHsd * C57BL/6	abnormal neural fold elevation formation	J:167065
	curly tail	J:167065
	embryonic growth retardation	J:167065
	embryonic lethality during organogenesis, complete penetrance	J:167065
	everted embryonic neuroepithelium	J:167065
	exencephaly	J:167065
	facial cleft	J:167065
	incomplete caudal neuropore closure	J:167065
	incomplete rostral neuropore closure	J:167065
	spina bifida	J:167065
Grhl2Gt(RRU622)Byg/Grhl2Gt(RRU622)Byg involves: 129P2/OlaHsd * C57BL/6	abnormal neural fold elevation formation	J:167065
	curly tail	J:167065
	embryonic growth retardation	J:167065
	embryonic lethality during organogenesis, complete penetrance	J:167065
	everted embryonic neuroepithelium	J:167065
	exencephaly	J:167065
	facial cleft	J:167065
	incomplete caudal neuropore closure	J:167065
	incomplete rostral neuropore closure	J:167065
	spina bifida	J:167065
Grhl2m1Nisw/Grhl2m1Nisw 129S1.B6-Grhl2m1Nisw	abnormal heart morphology	J:169829
	abnormal heart ventricle morphology	J:169829
	abnormal respiratory conducting tube morphology	J:169829
	decreased embryo size	J:169829
	decreased litter size	J:169829
	embryonic growth retardation	J:169829
	embryonic lethality during organogenesis, incomplete penetrance	J:169829
	exencephaly	J:169829
	facial cleft	J:169829
	lethality, incomplete penetrance	J:169829
	open neural tube	J:169829
	small lung lobe	J:169829
	thin ventricular wall	J:169829
	thoracoabdominoschisis	J:169829
Grhl2m1Nisw/Grhl2m1Nisw involves: C3HeB/FeJ * C57BL/6J	abnormal body wall morphology	J:169829
	abnormal cranium morphology	J:169829
	abnormal midface morphology	J:169829
	coloboma	J:169829
	exencephaly	J:169829
	facial cleft	J:169829
	interdigital webbing	J:169829
	lethality throughout fetal growth and development, complete penetrance	J:169829
	lethality, incomplete penetrance	J:169829
	open neural tube	J:169829
	split sternum	J:169829
	syndactyly	J:169829
Grhl2tm1.1Jane/Grhl2tm1.1Jane involves: 129S1/Sv * BALB/cJ * C57BL/6	abnormal neural fold elevation formation	J:164805
	cranioschisis	J:164805
	embryonic lethality during organogenesis, complete penetrance	J:164805
	facial cleft	J:164805
	incomplete caudal neuropore closure	J:164805