All terms in RGD
| Label | Id | Description |
|---|---|---|
| LOC108350659 | rgd:11367620 | |
| LOC102555809 | rgd:7677670 | |
| LOC100362965 | rgd:2323728 | |
| LOC100362967 | rgd:2323726 | |
| LOC108351215 | rgd:11367627 | |
| LOC103689957 | rgd:9197316 | |
| LOC100362976 | rgd:2323717 | |
| LOC100362978 | rgd:2323715 | [INVOLVED IN negative regulation of endopeptidase activity (inferred)] |
| LOC108348503 | rgd:11461516 | |
| LOC100362980 | rgd:2323713 | [ENCODES a protein that exhibits nucleic acid binding (inferred); zinc ion binding (inferred)] |
| LOC108353716 | rgd:11367638 | |
| LOC102550673 | rgd:7736453 | |
| LOC102550923 | rgd:7496434 | |
| LOC103693340 | rgd:9217344 | |
| LOC108348459 | rgd:11485594 | |
| LOC100362906 | rgd:2323787 | |
| LOC108348623 | rgd:11485595 | |
| Tex52 | rgd:2323784 | [ASSOCIATED WITH hyperphosphatemic familial tumoral calcinosis (ortholog); INTERACTS WITH bisphenol A (ortholog)] |
| LOC100362908 | rgd:2323785 | [ASSOCIATED WITH Charcot-Marie-Tooth disease type 2B (ortholog); Mitochondrial Complex I Deficiency, Nuclear Type 20 (ortholog); INTERACTS WITH 2-hydroxypropanoic acid (ortholog); aflatoxin B2 (ortholog); butanal (ortholog)] |
| Bsph2 | rgd:2323789 |