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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Clcn1
chloride channel, voltage-sensitive 1
MGI:88417
55 phenotypes from 12 alleles in 12 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Clcn1adr-mto2J/Clcn1adr-mto2J
BALB/cByJ-Clcn1adr-mto2J
decreased physiological sensitivity to xenobiotic J:112178
impaired muscle relaxation J:112061
impaired righting response J:112178
Clcn1adr-mto5J/Clcn1adr-mto5J
B6;129S-Fcgr2btm1Ttk
abnormal stationary movement J:94340
paraparesis J:94340
Clcn1adr-mto6J/Clcn1adr-mto6J
C57BL/6J-Clcn1adr-mto6J
forelimb paralysis J:87349
hindlimb paralysis J:87349
infertility J:87349
Clcn1adr-mto7J/Clcn1adr-mto7J
C57BL/6J-Clcn1adr-mto7J/J
limb grasping J:82238
muscle spasm J:82238
Clcn1adr-mto8J/Clcn1adr-mto8J
B6;C3Fe-Clcn1adr-mto8J/CxJ
abnormal gait J:120858
decreased body size J:120858
muscle spasm J:120858
postnatal growth retardation J:120858
Clcn1adr-mto9J/Clcn1adr-mto9J
C57BL/6J-Clcn1adr-mto9J/J
decreased body size J:134519
normal hearing/vestibular/ear phenotype J:134519
hindlimb paralysis J:134519
impaired muscle relaxation J:134519
sparse hair J:134519
normal vision/eye phenotype J:134519
Clcn1adr-mto/Clcn1adr-mto
SWR/J-Clcn1adr-mto/J
abnormal gait J:6814
abnormal muscle electrophysiology J:6814, J:14251
abnormal muscle physiology J:6814
abnormal righting response J:14251
abnormal voluntary movement J:6814, J:14251
axon degeneration J:6814
decreased body weight J:6814
impaired limb coordination J:6814
impaired muscle relaxation J:14251
increased skeletal muscle mass J:6814
kyphosis J:6814
normal muscle phenotype J:6814
reduced fertility J:6814
Clcn1adr/Clcn1adr
A2G-Clcn1adr
abnormal limb posture J:4480
abnormal muscle electrophysiology J:25830
abnormal muscle physiology J:4480, J:25830
abnormal skeletal muscle morphology J:25829
impaired muscle relaxation J:25830
impaired righting response J:4480, J:25830
impaired skeletal muscle contractility J:25830
male infertility J:4480
muscle twitch J:7524
postnatal growth retardation J:4480
premature death J:4480
reduced female fertility J:4480
Clcn1em1(IMPC)Mbp/Clcn1em1(IMPC)Mbp
C57BL/6NCrl-Clcn1em1(IMPC)Mbp/MbpMmucd
abnormal auditory brainstem response J:211773
abnormal behavior J:211773
abnormal eye morphology J:211773
abnormal gait J:211773
decreased body length J:211773
decreased exploration in new environment J:211773
decreased grip strength J:211773
decreased heart weight J:211773
decreased leukocyte cell number J:211773
decreased locomotor activity J:211773
decreased mean platelet volume J:211773
decreased monocyte cell number J:211773
decreased prepulse inhibition J:211773
decreased startle reflex J:211773
decreased thigmotaxis J:211773
decreased vertical activity J:211773
microphthalmia J:211773
tremors J:211773
Clcn1em1Btlr/Clcn1em1Btlr
C57BL/6J-Clcn1em1Btlr
abnormal vertebral column morphology J:307652
decreased body size J:307652
Clcn1m1Anu/Clcn1m1Anu
involves: C57BL/6 * CBA/H
abnormal gait J:104190
abnormal sensory capabilities/reflexes/nociception J:104190
ataxia J:104190
muscle hypertonia J:104190
paraparesis J:104190
Clcn1m1Btlr/Clcn1m1Btlr
C57BL/6J-Clcn1m1Btlr
abnormal vertebral column morphology J:307652
decreased body size J:307652

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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