30 phenotypes from 7 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Gabpaem2(IMPC)Mbp/Gabpa+ C57BL/6N-Gabpaem2(IMPC)Mbp/Ucd	anophthalmia	J:211773
	hemorrhage	J:211773
	increased circulating bilirubin level	J:211773
	microcephaly	J:211773
	microphthalmia	J:211773
	polydactyly	J:211773
	spina bifida	J:211773
	syndactyly	J:211773
Gabpaem2(IMPC)Mbp/Gabpaem2(IMPC)Mbp C57BL/6N-Gabpaem2(IMPC)Mbp/Ucd	abnormal cranium morphology	J:211773
	abnormal ear morphology	J:211773
	abnormal facial morphology	J:211773
	anophthalmia	J:211773
	hemorrhage	J:211773
	microcephaly	J:211773
	microphthalmia	J:211773
	polydactyly	J:211773
	preweaning lethality, complete penetrance	J:211773
	spina bifida	J:211773
	syndactyly	J:211773
GabpaGt(XH074)Byg/GabpaGt(XH074)Byg involves: 129P2/OlaHsd * C57BL/6	decreased fetal size	J:92671
	decreased thymocyte number	J:92671
	lethality throughout fetal growth and development, complete penetrance	J:92671
	small thymus	J:92671
Gabpatm1.1Sjb/Gabpatm1.1Sjb involves: 129S6/SvEvTac * C57BL/6	embryonic lethality, complete penetrance	J:121823
Gabpatm1Agro/Gabpatm1Agro involves: 129	normal embryo phenotype	J:126422
Gabpatm1Agro/Gabpatm1Agro involves: 129	abnormal cell cycle checkpoint function	J:126422
	decreased DNA replication	J:126422
	decreased fibroblast proliferation	J:126422
	increased cell mass	J:126422
Gabpatm1Pjh/Gabpatm1Pjh Tg(ACTA1-cre)79Jme/0 involves: 129X1/SvJ * C57BL/6 * SJL	abnormal channel response	J:121356
	abnormal neuromuscular synapse morphology	J:121356
	abnormal PNS synaptic transmission	J:121356
	abnormal synaptic acetylcholine release	J:121356
	decreased neurotransmitter release	J:121356
	normal muscle phenotype	J:121356
Gabpatm1Rist/Gabpatm1Rist 129X1/SvJ-Gabpatm1Rist	prenatal lethality, complete penetrance	J:91600
Gabpatm1Sjb/Gabpatm1.1Sjb Tg(ACTA1-cre)79Jme/0 involves: 129S6/SvEvTac * C57BL/6	no abnormal phenotype detected	J:121823