Symbol Name ID |
Gne
glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase MGI:1354951 |
Darker colors indicate more annotations |
Human Phenotypes | Spasticity |
Ataxia |
Poor fine motor coordination |
Athetosis |
Attention deficit hyperactivity disorder |
Delayed speech and language development |
Dysarthria |
Intellectual disability |
Intellectual disability, mild |
Sleep apnea |
Gait disturbance |
Inability to walk |
Global developmental delay |
Seizure |
Disease(s) Associated with GNE | ||||||||||||||
GNE myopathy | ||||||||||||||
sialuria |
Mouse Phenotypes | intracranial hemorrhage |
spinal hemorrhage |
abnormal neural tube morphology |
decreased prepulse inhibition |
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Availability | Mouse Genotype | ||||
Gneem1(IMPC)Mbp/Gneem1(IMPC)Mbp | |||||
Gneem1Lx/Gneem1Lx | |||||
Gneem1(IMPC)Mbp/Gne+ |
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 09/03/2024 MGI 6.24 |
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