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Symbol
Name
ID

Sbf1
SET binding factor 1
MGI:1925230

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Onion bulb formation	Myelin outfoldings	Brain atrophy	Decreased nerve conduction velocity	Intellectual disability	Areflexia	Gait disturbance	Loss of ambulation	Muscle fibrillation	Distal sensory impairment
Disease(s) Associated with SBF1
Charcot-Marie-Tooth disease type 4B3

Mouse Phenotypes		abnormal brain morphology	decreased brain weight	decreased brain size	abnormal axon radial sorting	abnormal sciatic nerve morphology	decreased prepulse inhibition
Availability	Mouse Genotype	abnormal brain morphology	decreased brain weight	decreased brain size	abnormal axon radial sorting	abnormal sciatic nerve morphology	decreased prepulse inhibition
	Sbf1^em1(IMPC)Mbp/Sbf1^em1(IMPC)Mbp
	Sbf1^em1Frobi/Sbf1^em1Frobi

Contributing Projects: 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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