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Symbol
Name
ID

Trpm7
transient receptor potential cation channel, subfamily M, member 7
MGI:1929996

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Bulbar palsy	Abnormal lower motor neuron morphology	Amyotrophic lateral sclerosis	Cerebral atrophy	Parkinsonism	Paralysis	Dementia
Disease(s) Associated with TRPM7
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1

Mouse Phenotypes		seizures	decreased sensory neuron number	small dorsal root ganglion	abnormal channel response
Availability	Mouse Genotype	seizures	decreased sensory neuron number	small dorsal root ganglion	abnormal channel response
	Trpm7^tm1Agry/Trpm7⁺
	Trpm7^tm1Clph/Trpm7^tm1Clph Tg(Pax3-cre)1Joe/0 (conditional)

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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