27 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Smarcc1tm1Rhs/Smarcc1+ involves: 129S4/SvJaeSor * C57BL/6	abnormal diencephalon morphology	J:72635
	abnormal embryonic neuroepithelial layer differentiation	J:72635
	abnormal forebrain morphology	J:72635
	abnormal lateral ventricle morphology	J:72635
	abnormal neural fold elevation formation	J:72635
	abnormal telencephalon morphology	J:72635
	abnormal third ventricle morphology	J:72635
	exencephaly	J:72635
Smarcc1tm1Rhs/Smarcc1tm1Rhs involves: 129S4/SvJaeSor * C57BL/6	abnormal embryonic tissue morphology	J:72635
	abnormal inner cell mass morphology	J:72635
	absent egg cylinders	J:72635
	absent endoderm	J:72635
	embryonic lethality between implantation and somite formation, complete penetrance	J:72635
Smarcc1tm2.1Rhs/Smarcc1tm2.1Rhs Tg(Mx1-cre)1Cgn/0 involves: BALB/c * C57BL/6 * CBA	abnormal bone marrow cell morphology/development	J:184060
	abnormal common lymphocyte progenitor cell morphology	J:184060
	abnormal immature B cell morphology	J:184060
	abnormal immunoglobulin heavy chain V(D)J recombination	J:184060
	abnormal pre-B cell morphology	J:184060
	abnormal pro-B cell morphology	J:184060
	arrested B cell differentiation	J:184060
	decreased B cell number	J:184060
	decreased B cell proliferation	J:184060
	decreased early pro-B cell number	J:184060
	decreased follicular B cell number	J:184060
	decreased late pro-B cell number	J:184060
	decreased pro-B cell number	J:184060
	increased B cell apoptosis	J:184060