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Symbol
Name
ID
Dst
dystonin
MGI:104627
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties
Poor suck
Bilateral vocal cord paresis
Disease(s) Associated with DST
hereditary sensory and autonomic neuropathy type 6

Mouse Phenotypes
behavior/neurological phenotype
decreased aggression
abnormal motor capabilities/coordination/movement
abnormal postural reflex
impaired righting response
abnormal response to tactile stimuli
unresponsive to tactile stimuli
decreased startle reflex
limb grasping
athetotic walking movements
dystonia
tremors
abnormal motor coordination/balance
ataxia
impaired balance
impaired coordination
impaired limb coordination
weakness
abnormal posture
head tilt
abnormal locomotor activation
abnormal gait
decreased locomotor activity
positive geotaxis
paresis
stereotypic behavior
seizures
Availability Mouse Genotype
Dstdt-23Rbrc/Dstdt-23Rbrc
Dstdt-30J/Dstdt-30J
Dstdt-31J/Dstdt-31J
Dstdt-32J/Dstdt-32J
Dstdt-33J/Dstdt-33J
Dstdt-35J/Dstdt-35J
Dstdt-36J/Dstdt-36J
Dstdt-37J/Dstdt-37J
Dstdt-38J/Dstdt-38J
Dstdt-39J/Dstdt-39J
Dstdt-alb/Dstdt-alb
Dstdt-J/Dstdt-J
Dstdt/Dstdt
DstGt(E182H05)Wrst/DstGt(E182H05)Wrst
Dstm1Btlr/Dstm1Btlr
Dstm2Btlr/Dstm2Btlr *
Dstm3Btlr/Dstm3Btlr
DstTg4/DstTg4
Dsttm1b(EUCOMM)Wtsi/Dsttm1b(EUCOMM)Wtsi
Dsttm1Efu/Dsttm1Efu
Dsttm1b(EUCOMM)Wtsi/Dst+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory