hasPhenotype

185 triples
GPTKB property

Alternative names (5)
associated phenotype associatedWithPhenotype has phenotype phenotype phenotypes

Random triples
Subject Object
gptkb:SHFM4 limb malformation
gptkb:SOD1-G93A_mouse progressive motor neuron degeneration
gptkb:MGI:96433 increased tumor incidence
gptkb:BALB/cJ high IgE response
gptkb:YDR179C defective transcriptional regulation
gptkb:YGL195W petite negative
gptkb:OMIM_109700 elevated sweat chloride
gptkb:Temple-Baraitser_syndrome broad nasal bridge
gptkb:Fanconi_anemia,_complementation_group_M congenital abnormalities
gptkb:OMIM:607709 progressive muscle weakness
gptkb:CYP2D6 ultrarapid metabolizer
gptkb:MIM_109700 chronic respiratory infections
gptkb:FBgn0000575 white eye color
gptkb:AGTR2_gene intellectual disability (in some mutations)
gptkb:Duffy_antigen Fy(a-b-)
gptkb:Nr1h3 impaired lipid homeostasis
gptkb:LCA10 photophobia
gptkb:Oca2_(mouse) pink eyes
gptkb:SOD1-G93A_transgenic_mouse reduced lifespan
gptkb:FBgn0000577 viability

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