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RET
Generet proto-oncogene
Encodes
The protein product this gene encodes, reached through the canonical GENE→PROTEIN (encodes) relation. Its biology, drugs, indications, trials and therapeutic evidence live on the protein's own page.
Also known as
Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.
HSCR1 · MEN2A · MTC1 · MEN2B · PTC · CDHF12 · RET51 · CDHR16
View full nomenclature history (13)Hide
HSCR1, MEN2A, MTC1, MEN2B
PTC, CDHF12, RET51, CDHR16
multiple endocrine neoplasia and medullary thyroid carcinoma 1, Hirschsprung disease 1
cadherin-related family member 16, RET receptor tyrosine kinase, rearranged during transfection
Associated diseases
Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.
Gene family
HGNC gene-group membership.
Cadherin relatedRet proto-oncogene family
Provenance
HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-02-19.
Open TargetsGene–disease associations from the Open Targets Platform.