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Symbol
Name
ID

Kif1b
kinesin family member 1B
MGI:108426

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Facial palsy

Horner syndrome

Decreased number of peripheral myelinated nerve fibers

Onion bulb formation

Axonal degeneration/regeneration

Peripheral axonal atrophy

Peripheral axonal neuropathy

Spinal cord compression

Neuroblastoma

Neoplasm of the nervous system

Ataxia

Myoclonus

Decreased motor nerve conduction velocity

Irritability

Areflexia

Hyporeflexia

Antalgic gait

Steppage gait

Peripheral neuropathy

Distal sensory impairment

Disease(s) Associated with KIF1B

Charcot-Marie-Tooth disease type 2A1

neuroblastoma

Mouse Phenotypes		decreased brain size	abnormal brain commissure morphology	abnormal brainstem morphology	abnormal hippocampus morphology	decreased neuron number	abnormal synaptic vesicle number	abnormal spinal cord ventral horn morphology	abnormal axonal transport
Availability	Mouse Genotype	decreased brain size	abnormal brain commissure morphology	abnormal brainstem morphology	abnormal hippocampus morphology	decreased neuron number	abnormal synaptic vesicle number	abnormal spinal cord ventral horn morphology	abnormal axonal transport
	Kif1b^tm1Noh/Kif1b^tm1Noh
	Kif1b^tm1Noh/Kif1b⁺

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 04/23/2024 MGI 6.23