|
Symbol Name ID |
Nexmif
neurite extension and migration factor MGI:2148050 |
| Darker colors indicate more annotations |
| Human Phenotypes | Secondary microcephaly |
Drooling |
Lower limb spasticity |
Ataxia |
Hypsarrhythmia |
Reduced eye contact |
Absent speech |
Delayed speech and language development |
Stuttering |
Anxiety |
Reduced social reciprocity |
Autistic behavior |
Bulimia |
Aggressive behavior |
Hyperactivity |
Motor stereotypy |
Stereotypical body rocking |
Bruxism |
Stereotypical hand wringing |
Recurrent hand flapping |
Self-biting |
Intellectual disability |
Global developmental delay |
Delayed ability to sit |
Bilateral tonic-clonic seizure |
Generalized non-motor (absence) seizure |
Generalized myoclonic seizure |
Atonic seizure |
Infantile spasms |
Tonic seizure |
Status epilepticus |
| Disease(s) Associated with NEXMIF | |||||||||||||||||||||||||||||||
| non-syndromic X-linked intellectual disability 98 |
| Mouse Phenotypes | seizures |
decreased CNS synapse formation |
decreased dendritic spine density |
increased dendritic spine length |
abnormal dendritic stubby spine morphology |
abnormal dendritic thin spine morphology |
abnormal hippocampal pyramidal neuron dendrite morphology |
abnormal CNS synaptic transmission |
enhanced paired-pulse facilitation |
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| Availability | Mouse Genotype | |||||||||
| Nexmiftm1(KOMP)Wtsi/Y | ||||||||||
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 05/21/2024 MGI 6.23 |
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