hasPhenotype

185 triples
GPTKB property

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

Random triples
Subject Object
gptkb:FUS_transgenic_mouse muscle weakness
gptkb:Duffy_antigen Fy(a+b+)
gptkb:Fanconi_anemia,_complementation_group_C skeletal anomalies
gptkb:YGL100W transcriptional regulation defect
gptkb:Duffy_antigen Fy(a+b-)
gptkb:chr2q37.3 gptkb:brachydactyly
gptkb:FBgn0000095 white eyes
gptkb:Temple-Baraitser_syndrome thick vermilion of lips
gptkb:LCA10 amaurosis
gptkb:SOD1-G93A_transgenic_mouse reduced lifespan
gptkb:OMIM:607709 respiratory failure
gptkb:SHFM4 limb malformation
gptkb:Immunodeficiency_18 impaired B cell function
gptkb:BALB/cJ albino
gptkb:Fanconi_anemia,_complementation_group_D2 developmental delay
gptkb:FBgn0003461 wingless phenotype
gptkb:Fanconi_anemia,_complementation_group_D2 skeletal anomalies
gptkb:Drosophila_lethal(2)_giant_larvae_(lgl) lethality in homozygous mutants
gptkb:splashed_white white face
gptkb:OMIM:607709 dysphagia

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