RET - Gene browser

RET

ret proto-oncogene

HCNC Approved Symbol: RET (HGNC:9967)
Genomic Coordinates: 10:43,077,069 - 43,130,351 (10q11.21)
Synonyms: PTC, CDHF12, RET51, CDHR16, HSCR1, MEN2A, MTC1, MEN2B
Disease Associations: This gene is associated with the following 6 diseases in OMIM.

12Patients

In total, 12 patients were diagnosed with a variant in the RET gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

012
Patient count

Global developmental delay: 3 (25.0%)
Patient Count: 3 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (25.0%)
Unilateral renal agenesis: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)
Total colonic aganglionosis: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)
Chronic constipation: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)
Abdominal distension: 1 (8.3%)
Patient Count: 1 (8.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (8.3%)