paired box 8
| GO Term | Evidence Code | PMID |
|---|---|---|
| urogenital system development | ||
| branching involved in ureteric bud morphogenesis | ||
| kidney development | ||
| mesonephros development | ||
| ventricular septum development |
| InterPro |
|---|
| Homeobox-like domain superfamily |
| PAX family |
| Paired domain |
| Winged helix-like DNA-binding domain superfamily |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050328 | congenital hypothyroidism | |
| DOID:0070124 | congenital nongoitrous hypothyroidism 2 |
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 5076 | FB:FBgn0005561 | ||
| 7849 | Xenbase:XB-GENE-483693 | ||
| 18510 | MOUSE33441 | ||
| 60637 | DANRE37589 | ||
| 81819 | RATNO27897 | ||
| 403927 | CANLF05127 | ||
| 459503 | PANTR28502 | ||
| 534661 | BOVIN02503 | ||
| 701906 | MACMU07223 | ||
| 100026381 | MONDO08060 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 4, 2025