Symbol Name ID |
Sbf2
SET binding factor 2 MGI:1921831 |
Darker colors indicate more annotations |
Human Phenotypes | Areflexia of lower limbs |
Areflexia of upper limbs |
Difficulty walking |
Decreased number of peripheral myelinated nerve fibers |
Onion bulb formation |
Segmental peripheral demyelination/remyelination |
Myelin outfoldings |
Poor fine motor coordination |
Tremor |
Vocal cord paralysis |
Decreased motor nerve conduction velocity |
Decreased distal sensory nerve action potential |
Autistic behavior |
Areflexia |
Hyporeflexia |
Inability to walk |
Steppage gait |
Tip-toe gait |
Motor delay |
Specific learning disability |
Paresthesia |
Distal sensory impairment |
Disease(s) Associated with SBF2 | ||||||||||||||||||||||
Charcot-Marie-Tooth disease type 4B2 |
Mouse Phenotypes | abnormal axon morphology |
abnormal myelin sheath morphology |
neuron degeneration |
abnormal action potential |
abnormal nerve conduction |
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Availability | Mouse Genotype | |||||
Sbf2Gt(RRF511)Byg/Sbf2Gt(RRF511)Byg | ||||||
Sbf2Gt(XH212)Byg/Sbf2Gt(XH212)Byg |
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 05/14/2024 MGI 6.23 |
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