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XB-GENEPAGE-492527
trpm1 transient receptor potential cation channel subfamily M member 1
Expression Phenotypes
Gene expression phenotype annotations where the gene of interest has been
disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from
differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1,
FDR <= 0.05 and an absolute LogFC >= 2.
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| Computed annotations: trpm1 assayed (4 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (14 sources): Abnormal electroretinogram, Abnormal fundus morphology, Abnormal retinal morphology, Abnormality of macular pigmentation, Congenital stationary night blindness, Dry skin, Eczematoid dermatitis, High myopia, Myopia, Nyctalopia, [+] |
| Mouse (6 sources): abnormal channel response, abnormal cone electrophysiology, abnormal eye electrophysiology, abnormal rod electrophysiology, limb grasping, vision/eye phenotype |
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View all ortholog results at Monarch |