| Gene ID | Entry | Entry Name | Protein Name | Type | Information | 176091 | P10038 | MAB5_CAEEL | Homeobox protein mab-5 (Protein male abnormal 5) | DISRUPTION PHENOTYPE | Defective QL neuroblast daughter cell migration (PubMed:8898225). Lin-39 and mab-5 double mutants have reduced sex myoblast specific expression of sem-2 in the developing mesoderm (PubMed:21307099). {ECO:0000269|PubMed:21307099, ECO:0000269|PubMed:8898225}. |
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