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General information
Gene symbol RET
Gene name ret proto-oncogene
Chromosome 10
Chromosomal band q11.2
Imprinted Not imprinted
Genomic reference LRG_363
Transcript reference NM_020630.4, NM_020975.4, XM_011540027.1
Associated with diseases FMTC
Citation reference(s) -
Curators (3) Savvas Nikolaou, Carsten W Lederer and Anastasia Raoukka
Total number of public variants reported 1
Unique public DNA variants reported 1
Individuals with public variants 0
Hidden variants 0
Date created June 22, 2016
Date last updated June 29, 2016
Version RET:160629

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 FMTC (Familial Medullary Thyroid Carcinoma)
HGMD RET
GeneCards RET
GeneTests RET


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000265 10 transcript variant 4 NM_020630.4 NP_065681.1 1
00000264 10 transcript variant 2 NM_020975.4 NP_066124.1 0
00000266 10 transcript variant X1 XM_011540027.1 XP_011538329.1 0


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