59 phenotypes from 9 alleles in 13 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
L1camtm1(tTA)Msch/L1cam+ 129.Cg-L1camtm1(tTA)Msch	abnormal behavioral response to light	J:227318
	abnormal social investigation	J:227318
	normal behavior/neurological phenotype	J:227318
	increased grooming behavior	J:227318
L1camtm1(tTA)Msch/Y involves: 129 * C57BL/6J	abnormal brain ventricle morphology	J:107878
	abnormal cerebral aqueduct morphology	J:107878
	abnormal hippocampus morphology	J:107878
	cerebellum atrophy	J:107878
	decreased body size	J:107878
	enlarged cranium	J:107878
	hydrocephaly	J:107878
	thin cerebral cortex	J:107878
L1camtm1.1Pfm/Y Not Specified	abnormal axon guidance	J:131051
	abnormal retina ganglion cell morphology	J:131051
	normal nervous system phenotype	J:131051
L1camtm1.1Pfm/L1camtm1.1Pfm Not Specified	abnormal axon guidance	J:131051
	abnormal axon morphology	J:131051
	abnormal retina ganglion cell morphology	J:131051
	normal nervous system phenotype	J:131051
L1camtm1.1Vlem/L1camtm1.1Vlem 129S2.Cg-L1camtm1.1Vlem	normal nervous system phenotype	J:89300
	prenatal lethality, incomplete penetrance	J:89300
L1camtm1.1Vlem/L1camtm1.1Vlem B6.Cg-L1camtm1.1Vlem	hydrocephaly	J:89300
	postnatal lethality, complete penetrance	J:89300
	prenatal lethality, incomplete penetrance	J:89300
L1camtm1Fmo/Y Tg(Camk2a-cre)1Gsc/0 involves: 129/Sv * C57BL/6	abnormal CNS synaptic transmission	J:86626
	abnormal spatial learning	J:86626
	decreased anxiety-related response	J:86626
	hyperactivity	J:86626
	increased exploration in new environment	J:86626
	increased vertical activity	J:86626
L1camtm1Mtei/Y either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	abnormal motor capabilities/coordination/movement	J:43838
	abnormal neuron morphology	J:43838
	abnormal response to tactile stimuli	J:43838
	abnormal Schwann cell morphology	J:43838
	abnormal thermal nociception	J:43838
	decreased body size	J:43838
	decreased corticospinal tract size	J:43838
	decreased grip strength	J:43838
	enlarged brain ventricles	J:43838
	enophthalmos	J:43838
	impaired limb coordination	J:43838
L1camtm1Mtei/Y involves: 129	normal nervous system phenotype	J:136656
L1camtm1Mtei/Y involves: 129 * C57BL/6J	abnormal cerebral aqueduct morphology	J:107878
	abnormal hippocampus morphology	J:107878
	cerebellum atrophy	J:107878
	decreased body size	J:107878
	enlarged brain ventricles	J:107878
	enlarged cranium	J:107878
	hydrocephaly	J:107878
	thin cerebral cortex	J:107878
L1camtm1Sor/Y either: 129S7/SvEvBrd-L1camtm1Sor or (129S7/SvEvBrd * C57BL/6J)F1	abnormal axon guidance	J:45013
	abnormal coat/hair pigmentation	J:45013
	abnormal corticospinal tract morphology	J:45013
	abnormal motor capabilities/coordination/movement	J:45013
	decreased body size	J:45013
	enophthalmos	J:45013
	excessive tearing	J:45013
	hindlimb paralysis	J:45013
	long toenails	J:45013
	male infertility	J:45013
	normal mortality/aging	J:45013
	normal nervous system phenotype	J:45013
	prenatal lethality, incomplete penetrance	J:45013
	normal reproductive system phenotype	J:45013
	slow postnatal weight gain	J:45013
L1camtm1Sor/Y involves: 129S7/SvEvBrd	abnormal axon extension	J:47995
	abnormal brain morphology	J:47995
	abnormal cerebellum morphology	J:47995
	abnormal cerebral aqueduct morphology	J:47995
	abnormal fourth ventricle morphology	J:47995
	abnormal sensory neuron innervation pattern	J:137627
	abnormal social/conspecific interaction behavior	J:47995
	abnormal somatic nervous system physiology	J:137627
	abnormal spatial learning	J:47995
	abnormal spinal cord dorsal horn morphology	J:137627
	cerebellum vermis hypoplasia	J:47995
	decreased body weight	J:47995
	decreased locomotor activity	J:47995
	dilated lateral ventricle	J:47995
	enlarged fourth ventricle	J:47995
	impaired coordination	J:47995
	increased thigmotaxis	J:47995
L1camtm2.1Vlem/Y either: 129S4.129S2-L1camtm2.1Vlem or B6.129S4-L1camtm2.1Vlem	normal behavior/neurological phenotype	J:197240
	normal mortality/aging	J:197240
	normal nervous system phenotype	J:197240
L1camtm3.1Vlem/Y either: 129S4.129S2-L1camtm3.1Vlem or B6.129S4-L1camtm3.1Vlem	abnormal neurite morphology	J:197240
	normal behavior/neurological phenotype	J:197240
	impaired coordination	J:197240
	normal mortality/aging	J:197240
	normal nervous system phenotype	J:197240
L1camtm4.1Vlem/Y either: 129S4.129S2-L1camtm4.1Vlem or B6.129S4-L1camtm4.1Vlem	abnormal neurite morphology	J:197240
	normal behavior/neurological phenotype	J:197240
	impaired coordination	J:197240
	normal mortality/aging	J:197240
	normal nervous system phenotype	J:197240