96 phenotypes from 23 alleles in 27 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Dstdt-23J/Dstdt-23J Not Specified	axonal dystrophy	J:11718
Dstdt-23Rbrc/Dstdt-23Rbrc involves: C3H/HeN * C57BL/6	abnormal brainstem morphology	J:251779
	abnormal locomotor activation	J:251779
	abnormal muscle physiology	J:251779
	abnormal neuron morphology	J:251779
	abnormal posture	J:251779
	abnormal sensory neuron morphology	J:251779
	abnormal spinal cord morphology	J:251779
	abnormal spinal nerve morphology	J:251779
	axonal spheroids	J:251779
	decreased locomotor activity	J:251779
	decreased myelin sheath thickness	J:251779
	dystonia	J:251779
	impaired limb coordination	J:251779
	impaired righting response	J:251779
	muscular atrophy	J:251779
	neurodegeneration	J:251779
	premature death	J:251779
	slow postnatal weight gain	J:251779
Dstdt-24J/Dstdt-24J involves: C57BL/6	axonal dystrophy	J:11718
Dstdt-27J/Dst+ B10.PL/(73NS)Sn-Dstdt-27J/J	abnormal axon morphology	J:48174
	abnormal myelination	J:48174
	abnormal Schwann cell morphology	J:48174
Dstdt-27J/Dstdt-27J B10.PL/(73NS)Sn-Dstdt-27J/J	abnormal axon morphology	J:48174, J:91505
	abnormal axonal transport	J:91505
	abnormal dorsal root ganglion morphology	J:91505
	abnormal dorsal spinal root morphology	J:47356, J:91495
	abnormal myelin sheath morphology	J:48174
	abnormal myelination	J:48174
	abnormal nervous system physiology	J:91505
	abnormal Schwann cell morphology	J:48174
	abnormal sciatic nerve morphology	J:91505
	abnormal sensory neuron morphology	J:47356
	abnormal somatic nervous system morphology	J:91505
	axon degeneration	J:91495, J:91505
	demyelination	J:48174, J:91495, J:91505
	peripheral nervous system degeneration	J:47356
Dstdt-30J/Dstdt-30J C57BL/6J-Dstdt-30J/J	dystonia	J:155853
	neurodegeneration	J:155853
	premature death	J:155853
Dstdt-31J/Dstdt-31J involves: DBA/1LacJ	dystonia	J:155854
	premature death	J:155854
Dstdt-32J/Dstdt-32J involves: 129S/Sv * 129S2/SvPas	abnormal somatic nervous system morphology	J:51014
	fecal incontinence	J:51014
	limb grasping	J:51014
	postnatal lethality	J:51014
	urinary incontinence	J:51014
Dstdt-33J/Dstdt-33J 129S1/Sv	ataxia	J:61053
	impaired coordination	J:61053
	postnatal lethality, complete penetrance	J:61053
	seizures	J:61053
Dstdt-35J/Dstdt-35J involves: 129S4/SvJae * C57BL/6	abnormal motor capabilities/coordination/movement	J:115254
Dstdt-36J/Dstdt-36J C57BL/6J-Dstdt-36J/J	abnormal posture	J:82238
Dstdt-37J/Dstdt-37J C57BL/6J-Dstdt-37J/J	axonal dystrophy	J:82238
	chromatolysis	J:82238
	decreased body size	J:82238
	decreased bone marrow cell number	J:82238
	decreased skeletal muscle fiber size	J:82238
	demyelination	J:82238
	dystonia	J:82238
	impaired righting response	J:82238
Dstdt-38J/Dstdt-38J involves: BALB/cByJ * C57BL/6J	abnormal posture	J:82238
	decreased body size	J:82238
	muscle spasm	J:82238
	normal reproductive system phenotype	J:82238
	weakness	J:82238
Dstdt-39J/Dstdt-39J involves: NOD	abnormal motor coordination/balance	J:157224
	cachexia	J:157224
	dystonia	J:157224
Dstdt-alb/Dstdt-alb BALB/cByJ-Dstdt-alb	abnormal nervous system morphology	J:64441
	abnormal neuron morphology	J:6316
	dystonia	J:64441
Dstdt-J/Dstdt-J B6C3Fe a/a-Dstdt-J/J	abnormal eye distance/ position	J:106403
	abnormal motor coordination/balance	J:106403
	abnormal postural reflex	J:106403
	abnormal posture	J:106403
	abnormal response to tactile stimuli	J:106403
	abnormal skin pigmentation	J:106403
	ataxia	J:106403
	decreased aggression	J:106403
	decreased body weight	J:106403
	decreased startle reflex	J:106403
	enophthalmos	J:106403
	impaired balance	J:106403
	impaired coordination	J:106403
	positive geotaxis	J:106403
	tremors	J:106403
Dstdt-J/Dstdt-J C3HeB/FeJ-Dstdt-J	abnormal motor coordination/balance	J:24773
	abnormal posture	J:24773
	athetotic walking movements	J:24773
	postnatal lethality, complete penetrance	J:24773
Dstdt/Dstdt involves: C57BL/6 * Q	demyelination	J:6491
Dstdt/Dstdt involves: Q	dystonia	J:5674
	impaired limb coordination	J:5674
	limb grasping	J:5674
	neurodegeneration	J:5674
	premature death	J:5674
Dstdt/Dstdt Q-Dstdt	abnormal nervous system morphology	J:5330
	axonal dystrophy	J:5330
	dystonia	J:64095
	gliosis	J:5330
	neurodegeneration	J:5330
	paresis	J:64095
	premature death	J:64095
DstGt(E182H05)Wrst/DstGt(E182H05)Wrst B6NCrj.129P2-DstGt(E182H05)Wrst	abnormal brainstem morphology	J:251779
	abnormal neuron morphology	J:251779
	abnormal neuron physiology	J:228781
	abnormal posture	J:251779
	abnormal spinal cord morphology	J:251779
	abnormal trigeminal motor nucleus morphology	J:228781
	axon degeneration	J:228781
	axonal spheroids	J:251779
	decreased brain size	J:228781
	decreased myelin sheath thickness	J:228781
	demyelination	J:228781
	dystonia	J:228781, J:251779
	impaired limb coordination	J:228781
	neurodegeneration	J:228781, J:251779
	premature death	J:228781
	small dorsal root ganglion	J:228781
DstGt(E182H05)Wrst/DstGt(E182H05)Wrst involves: 129P2/OlaHsd * ICR	abnormal muscle electrophysiology	J:228781, J:251779
Dstm1Btlr/Dstm1Btlr C57BL/6J-Dstm1Btlr	ataxia	J:218961
	decreased body weight	J:218961
Dstm2Btlr/Dstm2Btlr C57BL/6J-Dstm2Btlr	normal behavior/neurological phenotype	J:218962
	head tilt	J:218962
	stereotypic behavior	J:218962
Dstm3Btlr/Dstm3Btlr C57BL/6J-Dstm3Btlr	ataxia	J:218968
	impaired limb coordination	J:218968
DstTg4/Dst+ involves: CD-1	abnormal axon morphology	J:48174
	abnormal myelination	J:48174
	abnormal Schwann cell morphology	J:48174
DstTg4/DstTg4 involves: C57BL/6 * CD-1	abnormal axon morphology	J:209161
	abnormal dorsal root ganglion morphology	J:209161
	abnormal gait	J:209161
	abnormal muscle spindle morphology	J:209161
	abnormal neuromuscular synapse morphology	J:209161
	abnormal sensory neuron morphology	J:209161
	axon degeneration	J:209161
	blepharoptosis	J:209161
	conjunctivitis	J:209161
	impaired coordination	J:209161
	limb grasping	J:209161
	neuron degeneration	J:209161
	postnatal lethality	J:209161
	slow postnatal weight gain	J:209161
	small dorsal root ganglion	J:209161
DstTg4/DstTg4 involves: CD-1	abnormal axon morphology	J:48174
	abnormal circumvallate papillae morphology	J:104592
	abnormal dorsal root ganglion morphology	J:91495
	abnormal dorsal spinal root morphology	J:17844, J:47356
	abnormal glossopharyngeal ganglion morphology	J:104592
	abnormal gustatory papilla taste bud morphology	J:104592
	abnormal muscle physiology	J:55704
	abnormal myelin sheath morphology	J:48174
	abnormal myelination	J:17844, J:48174
	abnormal nervous system physiology	J:48174
	abnormal Schwann cell morphology	J:48174
	abnormal sensory neuron morphology	J:47356
	abnormal skeletal muscle fiber mitochondrial morphology	J:55704
	abnormal skeletal muscle fiber morphology	J:55704
	abnormal vagus nerve morphology	J:104592
	abnormal Z line morphology	J:55704
	impaired limb coordination	J:17844
	impaired skeletal muscle contractility	J:55704
	muscle weakness	J:55704
	peripheral nervous system degeneration	J:47356
	postnatal lethality	J:17844
Dsttm1b(EUCOMM)Wtsi/Dst+ C57BL/6N-Dsttm1b(EUCOMM)Wtsi/Bay	abnormal embryo size	J:211773
	persistence of hyaloid vascular system	J:211773
	unresponsive to tactile stimuli	J:211773
Dsttm1b(EUCOMM)Wtsi/Dsttm1b(EUCOMM)Wtsi C57BL/6N-Dsttm1b(EUCOMM)Wtsi/Bay	preweaning lethality, incomplete penetrance	J:211773
	unresponsive to tactile stimuli	J:211773
Dsttm1Efu/Dsttm1Efu involves: C57BL/6	abnormal myelin sheath morphology	J:24974
	alopecia	J:24974
	axon degeneration	J:24974
	blistering	J:24974
	delayed wound healing	J:24974
	dystonia	J:24974
	impaired righting response	J:24974
	kinked tail	J:24974
	muscular atrophy	J:24974
	premature death	J:24974