Alternative names (5)
associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypesRandom triples
| Subject | Object |
|---|---|
| gptkb:dpy-17 | dumpy |
| gptkb:Immunodeficiency_18 | impaired T cell function |
| gptkb:rd8_mouse | photoreceptor degeneration |
| gptkb:Fanconi_anemia,_complementation_group_D2 | increased risk of solid tumors |
| gptkb:MGI:96433 | increased tumor incidence |
| gptkb:Spontaneously_Hypertensive_Rat | hyperactivity |
| gptkb:C9orf72_mouse_model | cognitive impairment |
| gptkb:YNL005C | affects mRNA stability |
| gptkb:OMIM_109700 | exocrine pancreatic insufficiency |
| gptkb:Fanconi_anemia,_complementation_group_D2 | developmental delay |
| gptkb:Nr1h3 | altered cholesterol metabolism |
| gptkb:RhD | Rh positive |
| gptkb:WBGene00003001 | uncoordinated movement |
| gptkb:FUS_transgenic_mouse | neurodegeneration |
| gptkb:WBGene00000713 | uncoordinated movement |
| gptkb:MGI:96433 | embryonic lethality (homozygous null) |
| gptkb:LCA10 | photophobia |
| gptkb:Radiosensitive_SCID | failure to thrive |
| gptkb:Drosophila_enhancer_of_rudimentary | wing vein defects |
| gptkb:Neurotrophic_tyrosine_kinase_receptor_type_1_(mouse) | sensory neuron development |