Alternative names (5)
associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypesRandom triples
| Subject | Object |
|---|---|
| gptkb:WBGene00001052 | uncoordinated movement |
| gptkb:Spontaneously_Hypertensive_Rat | increased heart weight |
| gptkb:OMIM:607709 | respiratory failure |
| gptkb:FBgn0001981 | white eyes |
| gptkb:Splash_white | white markings on legs and underbelly |
| gptkb:MIM_109700 | elevated sweat chloride |
| gptkb:Oca2_(mouse) | diluted coat color |
| gptkb:Oncomouse | high incidence of cancer |
| gptkb:FUS_transgenic_mouse | motor neuron degeneration |
| gptkb:MGI:96067 | impaired DNA damage response |
| gptkb:OMIM:607709 | muscle atrophy |
| gptkb:AGTR2_gene | intellectual disability (in some mutations) |
| gptkb:Fanconi_anemia,_complementation_group_D2 | skeletal anomalies |
| gptkb:BALB/cJ | susceptible to developing plasmacytomas |
| gptkb:BALB/cJ | albino |
| gptkb:rs12913832 | iris pigmentation |
| gptkb:BALB/cByJ | Th2-biased immune response |
| gptkb:Spontaneously_Hypertensive_Rat | proteinuria |
| gptkb:Nf1_knockout_mouse | reduced lifespan |
| gptkb:MGI:96433 | impaired DNA damage response |