Symbol Name ID |
Ighmbp2
immunoglobulin mu DNA binding protein 2 MGI:99954 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased fetal movement |
Urinary incontinence |
Weak cry |
Disease(s) Associated with IGHMBP2 | |||
autosomal recessive distal hereditary motor neuronopathy 1 |
Mouse Phenotypes | abnormal food intake |
dysphagia |
impaired righting response |
limb grasping |
abnormal motor coordination/balance |
impaired coordination |
abnormal grip strength |
decreased grip strength |
abnormal gait |
hindlimb paralysis |
paraparesis |
allodynia |
increased thermal nociceptive threshold |
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Availability | Mouse Genotype | |||||||||||||
Ighmbp2em1Cll/Ighmbp2em1Cll | ||||||||||||||
Ighmbp2em1Cx/Ighmbp2em1Cx | ||||||||||||||
Ighmbp2em5Cx/Ighmbp2em5Cx | ||||||||||||||
Ighmbp2nmd-2J/Ighmbp2nmd-2J | ||||||||||||||
Ighmbp2nmd-2J/Ighmbp2nmd-2J Tg(Ttn-Ighmbp2)45Cx/? |
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Ighmbp2nmd-2J/Ighmbp2nmd-2J Tg(Ttn-Ighmbp2)108Cx/? |
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 08/21/2024 MGI 6.24 |
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