Known Diseases associated with this Protein: | CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL
| CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, WITH HIRSCHSPRUNG DISEASE
| HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
| MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA
| MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE
| MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB
| PHEOCHROMOCYTOMA, INCLUDED
| PHEOCHROMOCYTOMA, SOMATIC, IN
| RENAL AGENESIS
| THYROID CARCINOMA, FAMILIAL MEDULLARY
| THYROID CARCINOMA, FAMILIAL MEDULLARY, INCLUDED
| THYROID CARCINOMA, FAMILIAL MEDULLARY, INCLUDED;;
| THYROID CARCINOMA, SPORADIC MEDULLARY, INCLUDED;;
|
|  | Tips:  The Domains on the Default View are decided by the Domain's E-Value.  Clicking a check box will display or hide the correlated domain.  To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic. |
---|
|