RET gene homepage - CanVaS - A Greek Cancer Patient Genetic Variation Resource

To access more data, such as phenotypic and clinical characteristics of patients, contact us at canvas@rrp.demokritos.gr

CanVaS - A Greek Cancer Patient Genetic Variation Resource

RET (ret proto-oncogene)

LOVD v.3.0 Build 23 [ Current LOVD status ]
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	Curator: Despoina Kalfakakou

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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

Legend

Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

ID	Chr	Name	NCBI ID	NCBI Protein ID	Variants
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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