The RET gene homepage
| General information |
| Gene symbol |
RET |
| Gene name |
ret proto-oncogene |
| Chromosome |
10 |
| Chromosomal band |
q11.2 |
| Imprinted |
Unknown |
| Genomic reference |
NG_007489.1 |
| Transcript reference |
NM_020630.4, NM_020975.4 |
| Associated with diseases |
HSCR-1, MEN-2A, MEN-2B, MTC, pheochromocytoma, RHDA-1, Central hypoventilation syndrome, congenital, with or without Hirschsprung disease (Haddad syndrome) |
| Citation reference(s) |
- |
| Curators (1) |
Johan T. den Dunnen |
| Total number of public variants reported |
194 |
| Unique public DNA variants reported |
17 |
| Individuals with public variants |
35 |
| Hidden variants |
57 |
| Date created |
November 30, -0001 |
| Date last updated |
September 28, 2016 |
| Version |
RET:160928 |
| Links to other resources |
| External URL |
List of LSDBs for this gene The reference LOVD for this gene, if available |
| HGNC |
HGNC:9967 |
| Entrez Gene |
5979 |
| PubMed articles |
RET |
| OMIM - Gene |
164761 |
| OMIM - Diseases |
HSCR-1 (Hirschsprung disease, type 1 (HSCR-1)) MEN-2A (neoplasia, endocrine, multiple, type II1 (MEN-2A)) MEN-2B (neoplasia, endocrine, multiple, type IIb (MEN-2B)) MTC (carcinoma, thyroid, medullary, familial (MTC)) pheochromocytoma RHDA-1 (hypodysplasia/aplasia, renal, type 1 (RHDA-1)) Central hypoventilation syndrome, congenital, with or without Hirschsprung disease (Haddad syndrome) |
Active transcripts
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