RET gene homepage

General information
Gene symbol RET
Gene name ret proto-oncogene
Chromosome 10
Chromosomal band q11.21
Imprinted Unknown
Genomic reference LRG_363
Transcript reference NM_020630.4, NM_020975.4
Associated with diseases CCHS, HSCR1, MEN2A, MEN2B, MTC, Pheo
Citation reference(s) -
Curators (1) Despoina Kalfakakou
Total number of public variants reported 402
Unique public DNA variants reported 122
Individuals with public variants 391
Hidden variants 0
Date created May 20, 2020
Date last updated May 16, 2022
Version RET:220516

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 9967
Entrez Gene 5979
PubMed articles RET
OMIM - Gene 164761
OMIM - Diseases CCHS (Central hypoventilation syndrome)
HSCR1 (Hirschsprung disease, susceptibility to, 1)
MEN2A (Multiple endocrine neoplasia IIA)
MEN2B (Multiple endocrine neoplasia IIB)
MTC (Medullary thyroid carcinoma, familial)
Pheo (Pheochromocytoma, susceptibility to)

Active transcripts




NCBI ID     

NCBI Protein ID     

00000185 10 transcript variant 2 NM_020975.4 NP_066124.1 402
00000186 10 transcript variant 4 NM_020630.4 NP_065681.1 402

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