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_020975.4
Exon/intron information NM_020975.4 exon/intron table
Associated with diseases HSCR1, MEN2A, MEN2B, MTC, pheochromocytoma
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Angelo Minucci
Total number of public variants reported 227
Unique public DNA variants reported 137
Individuals with public variants 287
Hidden variants 4
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created April 29, 2010
Date last updated April 16, 2023
Version RET:230416

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_020975.4.
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
Homepage URL
HGNC 9967
Entrez Gene 5979
PubMed articles RET
OMIM - Gene 164761
OMIM - Diseases HSCR1 (Hirschsprung disease, type 1 (HSCR1))
MEN2A (neoplasia, endocrine, multiple, type II1 (MEN-2A))
MEN2B (neoplasia, endocrine, multiple, type IIb (MEN-2B))
MTC (carcinoma, thyroid, medullary, familial (MTC))
GeneCards RET
GeneTests RET
Orphanet RET

Active transcripts




NCBI ID     

NCBI Protein ID     

00017640 10 transcript variant 2 NM_020975.4 NP_066124.1 227

Copyright & disclaimer
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