| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Yellow pigmentation of the skin or sclera due to bilirubin, which in turn is the result of increased bilirubin concentration in the bloodstream. (Human Phenotype Ontology, HP_0000952) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000611 |
| Similar Terms | |
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11 gene mutations causing the jaundice phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| ANK1 | ankyrin 1, erythrocytic |
| FAH | fumarylacetoacetate hydrolase (fumarylacetoacetase) |
| FECH | ferrochelatase |
| FOXP3 | forkhead box P3 |
| HNF1A | HNF1 homeobox A |
| INVS | inversin |
| LAMA4 | laminin, alpha 4 |
| NR1H4 | nuclear receptor subfamily 1, group H, member 4 |
| ONECUT1 | one cut homeobox 1 |
| SPTA1 | spectrin, alpha, erythrocytic 1 |
| SPTB | spectrin, beta, erythrocytic |
