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

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
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


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00026580 10 transcript variant 2 NM_020975.4 NP_066124.1 194
00026581 10 transcript variant 4 NM_020630.4 NP_065681.1 194