Alternative names (5)
associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypesRandom triples
| Subject | Object |
|---|---|
| gptkb:Drosophila_enhancer_of_rudimentary | wing vein defects |
| gptkb:MGI:96677 | abnormal cell cycle |
| gptkb:OMIM_109700 | chronic pulmonary disease |
| gptkb:Splash_white | white markings on legs and underbelly |
| gptkb:YNL005C | affects mRNA stability |
| gptkb:Oca2_(mouse) | pink eyes |
| gptkb:Silver-Russell_syndrome_(mouse_model) | craniofacial abnormalities |
| gptkb:Neurotrophic_tyrosine_kinase_receptor_type_1_(mouse) | pain perception |
| gptkb:E._coli_REL606 | Ara- (arabinose negative) |
| gptkb:OMIM:607709 | dysphagia |
| gptkb:WBGene00003013 | paralyzed |
| gptkb:C9orf72_mouse_model | cognitive impairment |
| gptkb:46,XX_sex_reversal | gptkb:male |
| gptkb:BALB/cByJ | Th2-biased immune response |
| gptkb:Fanconi_anemia,_complementation_group_M | developmental delay |
| gptkb:Oncomouse | high incidence of cancer |
| gptkb:Spontaneously_Hypertensive_Rat | high blood pressure |
| gptkb:Beckwith-Wiedemann_syndrome_(mouse_model) | organomegaly |
| gptkb:SOD1-G93A_transgenic_mouse | reduced lifespan |
| gptkb:YGL195W | respiratory deficient when deleted |