53 phenotypes from 6 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Csktm1Sia/Csk+ involves: BALB/c * C57BL/6 * CBA	no abnormal phenotype detected	J:12623
Csktm1Sia/Csktm1Sia involves: BALB/c * C57BL/6 * CBA	abnormal cranial ganglia morphology	J:12623
	abnormal embryonic neuroepithelium morphology	J:12623
	abnormal heart development	J:12623
	abnormal neural tube morphology	J:12623
	abnormal otic vesicle development	J:12623
	absent nasal placodes	J:12623
	absent optic placodes	J:12623
	absent visceral yolk sac blood islands	J:12623
	absent vitelline blood vessels	J:12623
	cellular necrosis	J:12623
	normal cellular phenotype	J:12623
	decreased embryo size	J:12623
	decreased embryonic neuroepithelium thickness	J:12623
	delayed neural tube closure	J:12623
	embryo tissue necrosis	J:12623
	embryonic growth arrest	J:12623
	embryonic growth retardation	J:12623
	embryonic lethality during organogenesis, complete penetrance	J:12623
	incomplete caudal neuropore closure	J:12623
	incomplete embryo turning	J:12623
	incomplete rostral neuropore closure	J:12623
Csktm1Sor/Csk+ 129P2.129S7-Csktm1Sor	abnormal food preference	J:188631
	abnormal object recognition memory	J:188631
	abnormal social investigation	J:188631
	decreased anxiety-related response	J:188631
Csktm1Sor/Csktm1Sor either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	abnormal allantois morphology	J:12622
	abnormal cephalic neural fold morphology	J:12622
	absent notochord	J:12622
	caudal body truncation	J:12622
	decreased embryo size	J:12622
	embryonic lethality during organogenesis, complete penetrance	J:12622
	enlarged allantois	J:12622
	incomplete embryo turning	J:12622
	incomplete rostral neuropore closure	J:12622
	megacephaly	J:12622
	open neural tube	J:12622
	poor circulation	J:12622
	wavy neural tube	J:12622
Csktm1Tara/Csktm1Tara Tg(Mx1-cre)1Cgn/0 involves: 129P2/OlaHsd * C57BL/6 * CB20 * CBA	abnormal CD4-positive T cell differentiation	J:49654
	absent CD8-positive, alpha-beta T cells	J:49654
	enlarged thymus	J:49654
Csktm1Tara/Csktm2Tara Elanetm1(cre)Roes/Elane+ involves: 129P2/OlaHsd * CB20 * C57BL/6	abnormal granulocyte physiology	J:89716
	abnormal myelopoiesis	J:89716
	increased acute inflammation	J:89716
	increased susceptibility to bacterial infection	J:89716
Csktm2b(EUCOMM)Hmgu/Csk+ C57BL/6N-Csktm2b(EUCOMM)Hmgu/Bay	abnormal retina inner nuclear layer morphology	J:211773
	abnormal retina vasculature morphology	J:211773
	decreased total retina thickness	J:211773
Csktm2b(EUCOMM)Hmgu/Csktm2b(EUCOMM)Hmgu C57BL/6N-Csktm2b(EUCOMM)Hmgu/Bay	abnormal embryo development	J:211773
	abnormal embryo size	J:211773
	abnormal embryo turning	J:211773
	abnormal neural tube closure	J:211773
	embryonic growth retardation	J:211773
	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773
Csktm2Sia/Csktm2Sia involves: BALB/c * C57BL/6 * CBA	abnormal cranial ganglia morphology	J:12623
	abnormal lens induction	J:12623
	abnormal neural tube morphology	J:12623
	abnormal otic vesicle development	J:12623
	absent olfactory bulb	J:12623
	absent visceral yolk sac blood islands	J:12623
	absent vitelline blood vessels	J:12623
	cellular necrosis	J:12623
	normal cellular phenotype	J:12623
	decreased embryo size	J:12623
	embryo tissue necrosis	J:12623
	embryonic growth arrest	J:12623
	embryonic growth retardation	J:12623
	embryonic lethality during organogenesis, complete penetrance	J:12623
	incomplete embryo turning	J:12623
	incomplete rostral neuropore closure	J:12623
	open neural tube	J:12623