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Symbol
Name
ID

Sbf2
SET binding factor 2
MGI:1921831

Phenotype annotations related to nervous system

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
Availability	Mouse Genotype	abnormal axon morphology	abnormal myelin sheath morphology	neuron degeneration	abnormal action potential	abnormal nerve conduction
	Sbf2^{Gt(RRF511)Byg}/Sbf2^{Gt(RRF511)Byg}
	Sbf2^Gt(XH212)Byg/Sbf2^Gt(XH212)Byg

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 05/07/2024 MGI 6.23