Alternative names (5)
associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypesRandom 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 |