Alternative names (5)
associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypesRandom triples
| Subject | Object |
|---|---|
| gptkb:MGI:96067 | embryonic lethality (homozygous null) |
| gptkb:FUS_transgenic_mouse | motor neuron degeneration |
| gptkb:Temple-Baraitser_syndrome | delayed development |
| gptkb:SHFM4 | limb malformation |
| gptkb:OMIM_109700 | exocrine pancreatic insufficiency |
| gptkb:LCA10 | severe visual impairment |
| gptkb:YGL195W | petite negative |
| gptkb:OMIM:607709 | dysphagia |
| gptkb:chr2q37.3 | gptkb:intellectual_disability |
| gptkb:WBGene00002992 | paralyzed |
| gptkb:Nf1_knockout_mouse | abnormal neural development |
| gptkb:Fanconi_anemia,_complementation_group_D2 | developmental delay |
| gptkb:OMIM_109700 | male infertility |
| gptkb:cytochrome_P450_2D6 | poor metabolizer |
| gptkb:SOD1-G93A_mouse | reduced lifespan |
| gptkb:Nr1h3 | altered cholesterol metabolism |
| gptkb:subcortical_band_heterotopia | seizures |
| gptkb:46,XX_sex_reversal | gptkb:male |
| gptkb:Splash_white | white markings on legs and underbelly |
| gptkb:OMIM:160790 | elevated sweat chloride |