53 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tmem67b2b1163.1Clo/Tmem67b2b1163.1Clo C57BL/6J-Tmem67b2b1163.1Clo	atrioventricular septal defect	J:175213
	double outlet right ventricle	J:175213
	heart right ventricle hypoplasia	J:175213
	heterotaxia	J:175213
	interrupted aortic arch	J:175213
	polycystic kidney	J:175213
Tmem67b2b1291.1Clo/Tmem67b2b1291.1Clo C57BL/6J-Tmem67b2b1291.1Clo	heterotaxia	J:175213
	polycystic kidney	J:175213
	right-sided stomach	J:175213
	situs inversus with levocardia	J:175213
Tmem67em1(IMPC)J/Tmem67+ C57BL/6NJ-Tmem67em1(IMPC)J/Mmjax	increased exploration in new environment	J:211773
	increased grip strength	J:211773
Tmem67em1(IMPC)J/Tmem67em1(IMPC)J C57BL/6NJ-Tmem67em1(IMPC)J/Mmjax	preweaning lethality, complete penetrance	J:211773
Tmem67tm1Dgen/Tmem67tm1Dgen B6.129P2-Tmem67tm1Dgen	abnormal basal ganglion morphology	J:193837
	abnormal brain ependyma motile cilium morphology	J:193837
	abnormal centrosome morphology	J:193837
	abnormal cilium morphology	J:193837
	abnormal corpus callosum morphology	J:193837
	abnormal dorsal-ventral axis patterning	J:193837
	abnormal embryonic neuroepithelium morphology	J:193837
	abnormal forebrain development	J:193837
	abnormal hepatobiliary system development	J:193837
	abnormal midbrain development	J:193837
	abnormal nervous system morphology	J:193837
	abnormal neural fold morphology	J:193837
	abnormal neural tube morphology	J:193837
	abnormal neural tube ventricular layer morphology	J:193837
	abnormal posterior cranial fossa morphology	J:193837
	abnormal renal tubule epithelial cell primary cilium morphology	J:176174
	abnormal roof plate morphology	J:193837
	abnormal tegmentum morphology	J:193837
	absent anterior commissure	J:193837
	absent embryonic cilia	J:193837
	normal cellular phenotype	J:176174
	cerebellum vermis hypoplasia	J:193837
	decreased forebrain size	J:193837
	decreased hindbrain size	J:193837
	dilated fourth ventricle	J:193837
	encephalomeningocele	J:193837
	enlarged hippocampus	J:193837
	exencephaly	J:193837
	incomplete rostral neuropore closure	J:193837
	increased forebrain size	J:193837
	kidney cyst	J:176174, J:193837
	normal limbs/digits/tail phenotype	J:193837
	mandible hypoplasia	J:193837
	meningocele	J:193837
	microcephaly	J:193837
	neonatal lethality, incomplete penetrance	J:176174
	perinatal lethality	J:193837
	postnatal growth retardation	J:176174
	postnatal lethality	J:193837
	postnatal lethality, incomplete penetrance	J:176174
	semilobar holoprosencephaly	J:193837
	small cerebellum	J:193837