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XB-GENEPAGE-940168
kcnv2 potassium channel, voltage gated modifier subfamily V, member 2
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: kcnv2 assayed (1 source) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (9 sources): Astigmatism, Cone/cone-rod dystrophy, Horizontal nystagmus, Macular atrophy, Myopia, Nyctalopia, Photophobia, Scotoma, Strabismus |
Mouse (11 sources): abnormal cone electrophysiology, abnormal rod electrophysiology, decreased retina rod cell number, decreased total retina thickness, increased bone mineral content, increased lean body mass, increased retina apoptosis, no abnormal phenotype detected, short photoreceptor inner segment, short photoreceptor outer segment, [+] |
View all ortholog results at Monarch |