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Symbol
Name
ID

Prkcg
protein kinase C, gamma
MGI:97597

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes

Facial myokymia

Dysphagia

Cerebellar atrophy

Dysmetria

Gait ataxia

Progressive cerebellar ataxia

Dysarthria

Depression

Attention deficit hyperactivity disorder

Memory impairment

Mental deterioration

Hyperreflexia

Focal dystonia

Impaired vibration sensation at ankles

Disease(s) Associated with PRKCG

spinocerebellar ataxia type 14

Mouse Phenotypes		nervous system phenotype	abnormal Purkinje cell dendrite morphology	abnormal cerebellar molecular layer	abnormal innervation	abnormal excitatory postsynaptic currents	reduced long-term potentiation
Availability	Mouse Genotype	nervous system phenotype	abnormal Purkinje cell dendrite morphology	abnormal cerebellar molecular layer	abnormal innervation	abnormal excitatory postsynaptic currents	reduced long-term potentiation
	Prkcg^em1Jpka/Prkcg^em1Jpka
	Prkcg^tm1Stl/Prkcg^tm1Stl	*
	Prkcg^em1Jpka/Prkcg⁺

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 04/30/2024 MGI 6.23