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Symbol
Name
ID
Mtm1
X-linked myotubular myopathy gene 1
MGI:1099452
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Feeding difficulties in infancy
Dysphonia
Disease(s) Associated with MTM1
centronuclear myopathy

Mouse Phenotypes
behavior/neurological phenotype
abnormal motor capabilities/coordination/movement
abnormal physical strength
decreased grip strength
decreased vertical activity
hypoactivity
abnormal gait
hindlimb paralysis
abnormal vocalization
Availability Mouse Genotype
Mtm1Gt(OST290577)Lex/Y
Mtm1tm1.1Jman/Y
Mtm1tm1Itl/Y *

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory