hasPhenotype

URI: https://gptkb.org/prop/hasPhenotype

185 triples

GPTKB property

associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypes

Subject	Object
gptkb:YGL100W	transcriptional regulation defect
gptkb:Nr1h3	altered cholesterol metabolism
gptkb:Temple-Baraitser_syndrome	hypotonia
gptkb:Fanconi_anemia,_complementation_group_D2	skeletal anomalies
gptkb:WBGene00002963	uncoordinated movement
gptkb:Splash_white	blue eyes
gptkb:BALB/cJ	albino
gptkb:Fanconi_anemia,_complementation_group_M	congenital abnormalities
gptkb:OMIM:160790	exocrine pancreatic insufficiency
gptkb:Fanconi_anemia,_complementation_group_M	developmental delay
gptkb:Radiosensitive_SCID	recurrent infections
gptkb:Temple-Baraitser_syndrome	thick vermilion of lips
gptkb:Drosophila_melanogaster_(E(z))	homeotic transformation
gptkb:SOD1-G93A_transgenic_mouse	motor neuron degeneration
gptkb:OMIM:607709	fasciculations
gptkb:OMIM:607709	respiratory failure
gptkb:Nf1_knockout_mouse	increased tumor formation
gptkb:WBGene00003013	uncoordinated movement
gptkb:Drosophila_enhancer_of_rudimentary	wing vein defects
gptkb:Silver-Russell_syndrome_(mouse_model)	craniofacial abnormalities