51 phenotypes from 9 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Chat/Slc18a3tm1.1Vpra/Chat+ involves: 129S4/SvJae * C57BL/6J	abnormal miniature endplate potential	J:171696
	normal behavior/neurological phenotype	J:171696
	increased acetylcholine level	J:153908
Chat/Slc18a3tm1.1Vpra/Chat/Slc18a3tm1.1Vpra involves: 129S4/SvJae * C57BL/6J	abnormal miniature endplate potential	J:153908
	abnormal motor neuron innervation pattern	J:153908
	abnormal neuromuscular synapse morphology	J:153908
	abnormal skeletal muscle morphology	J:153908
	abnormal synaptic acetylcholine release	J:153908
	cyanosis	J:153908
	hypotonia	J:153908
	increased acetylcholine level	J:153908
	increased motor neuron number	J:153908
	kyphosis	J:153908
	neonatal lethality, complete penetrance	J:153908
	skeletal muscle atrophy	J:153908
	skeletal muscle fiber atrophy	J:153908
Chat/Slc18a3tm1.1Vpra/Chat/Slc18a3tm1.1Vpra Tg(Chat-COP4*H134R/EYFP,Slc18a3)6Gfng/0 involves: 129S4/SvJae * C57BL/6 * CBA	normal mortality/aging	J:197166
Chat/Slc18a3tm1.2Vpra/Chat/Slc18a3tm1.2Vpra involves: 129S4/SvJae * C57BL/6J	normal behavior/neurological phenotype	J:171696
Chat/Slc18a3tm1Vpra/Chat/Slc18a3tm1.1Vpra involves: 129S4/SvJae * C57BL/6J	abnormal miniature endplate potential	J:171696
	normal behavior/neurological phenotype	J:171696
	hyperactivity	J:171696
	increased vertical activity	J:171696
Chat/Slc18a3tm1Vpra/Chat/Slc18a3tm1Vpra involves: 129S4/SvJae * C57BL/6J	abnormal miniature endplate potential	J:171696
	normal behavior/neurological phenotype	J:171696
	hyperactivity	J:171696
Chattm1(cre)Lowl/Chat+ involves: 129S6/SvEvTac * C57BL/6	no abnormal phenotype detected	J:114556
Chattm1(cre/ERT)Nat/Chattm1(cre/ERT)Nat involves: 129 * C57BL/6	no abnormal phenotype detected	J:144315
Chattm1.1Jrs/Chattm1.1Jrs Not Specified	abnormal innervation pattern to muscle	J:91066
	abnormal muscle morphology	J:91066
	abnormal neuromuscular synapse morphology	J:91066
	abnormal phrenic nerve morphology	J:91066
	abnormal Schwann cell morphology	J:91066
	carpoptosis	J:91066
	diaphragmatic hernia	J:91066
	increased motor neuron number	J:91066
	kyphosis	J:91066
	neonatal lethality, complete penetrance	J:91066
	thin diaphragm muscle	J:91066
Chattm1Fhg/Chattm1Fhg involves: 129S2/SvPas * C57BL/6	abnormal innervation	J:81738
	abnormal neuromuscular synapse morphology	J:81738
	abnormal PNS synaptic transmission	J:81738
	carpoptosis	J:81738
	decreased fetal size	J:81738
	increased motor neuron number	J:81738
	kyphosis	J:81738
	perinatal lethality, complete penetrance	J:81738
	normal reproductive system phenotype	J:113236
Chattm1Fhg/Chattm1Fhg involves: 129S4/SvJae	increased motor neuron number	J:161300
Chattm1Jrs/Chattm1Jrs Tg(CAG-cre/Esr1*)1Lbe/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal innervation pattern to muscle	J:89596
	postnatal lethality, complete penetrance	J:89596
	weakness	J:89596
Chattm1Jrs/Chattm1Jrs Tg(CAG-cre/Esr1*)1Lbe/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	abnormal axon morphology	J:89596
	abnormal neuromuscular synapse morphology	J:89596
	postnatal lethality, complete penetrance	J:89596
	weakness	J:89596
Chattm1Mlt/Chattm1Mlt Tg(SLC18A3-cre)KMisa/0 involves: 129 * C57BL/6	abnormal gait	J:212048
	abnormal gastrocnemius morphology	J:212048
	abnormal habituation to a new environment	J:212048
	abnormal muscle morphology	J:212048
	abnormal soleus morphology	J:212048
	abnormal tail morphology	J:212048
	cornea opacity	J:212048
	decreased body weight	J:212048
	decreased locomotor activity	J:212048
	decreased vertical activity	J:212048
	kyphosis	J:212048
	muscle weakness	J:212048
	muscular atrophy	J:212048
	normal nervous system phenotype	J:212048
	premature death	J:212048
	rectal prolapse	J:212048
	skeletal muscle endomysial fibrosis	J:212048
	skeletal muscle fibrosis	J:212048
	tail dragging	J:212048
	tremors	J:212048