Global Variome shared LOVD
RET (ret proto-oncogene)
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
Curator:
Angelo Minucci
View all genes
View RET gene homepage
View graphs about the RET gene database
Create a new gene entry
View all transcripts
View all transcripts of gene RET
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene RET
View all variants in gene RET
Full data view for gene RET
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
View all individuals with variants in gene RET
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene RET
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene RET
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
All screenings for gene RET
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.
Template
: Template(s) used to detect the sequence variant; DNA (genomic DNA), RNA (cDNA) or protein
All options:
DNA
RNA = RNA (cDNA)
protein
? = unknown
Technique
: technique(s) used to identify the sequence variant.
All options:
? = unknown
ARMS = amplification refractory mutation system
arrayCGH = array for Comparative Genomic Hybridisation
arrayMET = array for methylation analysis
arraySEQ = array for resequencing
arraySNP = array for SNP typing
arrayCNV = array for Copy Number Variation (SNP and CNV probes)
ASO = allele-specific oligo hybridisation
BESS = Base Excision Sequence Scanning
CMC = Chemical Mismatch Cleavage
COBRA = Combined Bisulfite Restriction Analysis
CSCE = Conformation Sensitive Capillary Electrophoresis
CSGE = Conformation Sensitive Gel Electrophoresis
ddF = dideoxy Fingerprinting
DGGE = Denaturing-Gradient Gel-Electrophoresis
DHPLC = Denaturing High-Performance Liquid Chromatography
DOVAM = Detection Of Virtually All Mutations (SSCA variant)
DSCA = Double-Strand DNA Conformation Analysis
DSDI = Detection Small Deletions and Insertions
EMC = Enzymatic Mismatch Cleavage
expr = expression analysis
FISH = Fluorescent In-Situ Hybridisation
FISHf = fiberFISH
HD = HeteroDuplex analysis
HPLC = High-Performance Liquid Chromatography
IEF = IsoElectric Focussing
IHC = Immuno-Histo-Chemistry
Invader = Invader assay
MAPH = Multiplex Amplifiable Probe Hybridisation
MAQ = Multiplex Amplicon Quantification
MCA = Melting Curve Analysis, high-resolution (HRMA)
microscope = microscopic analysis (karyotype)
microsat = microsatellite genotyping
minigene = expression minigene construct
MIP = Molecular Inversion Probe amplification
MIPsm = single molecule Molecular Inversion Probe amplification
MLPA = Multiplex Ligation-dependent Probe Amplification
MLPA-ms = Multiplex Ligation-dependent Probe Amplification, methylation specific
MS = mass spectrometry
Northern = Northern blotting
NUC = nuclease digestion (RNAseT1, S1)
OM = optical mapping
PAGE = Poly-Acrylamide Gel-Electrophoresis
PCR = Polymerase Chain Reaction
PCRdd = PCR, digital droplet
PCRdig = PCR + restriction enzyme digestion
PCRh = PCR, haloplex
PCRlr = PCR, long-range
PCRm = PCR, multiplex
PCRms = PCR, methylation sensitive
PCRq = PCR, quantitative (qPCR)
PCRrp = PCR, repeat-primed (RP-PCR)
PCRsqd = PCR, semi-quantitative duplex
PE = primer extension (APEX, SNaPshot)
PEms = primer extension, methylation-sensitive single-nucleotide
PFGE = Pulsed-Field Gel-Electrophoresis (+Southern)
PTT = Protein Truncation Test
RFLP = Restriction Fragment Length Polymorphisms
RT-PCR = Reverse Transcription and PCR
RT-PCRq = Reverse Transcription and PCR, quantitative
SBE = Single Base Extension
SEQ = SEQuencing (Sanger)
SEQb = bisulfite SEQuencing
SEQp = pyroSequencing
SEQms = sequencing, methylation specific
SEQ-ON = next-generation sequencing - Oxford Nanopore
SEQ-NG = next-generation sequencing
SEQ-NG-RNA = next-generation sequencing RNA
SEQ-NG-H = next-generation sequencing - Helicos
SEQ-NG-I = next-generation sequencing - Illumina/Solexa
SEQ-NG-IT = next-generation sequencing - Ion Torrent
SEQ-NG-R = next-generation sequencing - Roche/454
SEQ-NG-S = next-generation sequencing - SOLiD
SEQ-PB = next-generation sequencing - Pacific Biosciences
SNPlex = SNPlex
Southern = Southern blotting
SSCA = Single-Strand DNA Conformation polymorphism Analysis (SSCP)
SSCAf = fluorescent SSCA (SSCP)
STR = Short Tandem Repeat
TaqMan = TaqMan assay
Western = Western blotting
- = not applicable
Tissue
: tissue type used for analysis
Remarks
: remarks regarding the screening like WGS (whole genome sequencing), WES (whole exome sequencing, gene panel (incl. a list of genes analysed), etc.
How to query this table
All list views have search fields which can be used to search data. You can search for a complete word or you can search for a part of a search term. If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify. Note that search terms are case-insensitive and that wildcards such as * are treated as normal text! For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.
Operator
Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
Arg Ser
all entries containing 'Arg' and 'Ser'
|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
Text
!=""
all entries with this field not empty
!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
>=
Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
To sort on a certain column, click on the column header or on the arrows. If that column is already selected to sort on, the sort order will be swapped. The column currently sorted on has a darker blue background color than the other columns. The up and down arrows next to the column name indicate the current sorting direction. When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.
75 entries on 1 page. Showing entries 1 - 75.
10 per page
25 per page
50 per page
100 per page
Legend
How to query
Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000036729
00036659
DNA
SEQ
-
-
1
Andreas Laner
0000036730
00036660
DNA
SEQ
-
-
1
Andreas Laner
0000036731
00036661
DNA
SEQ
-
-
1
Andreas Laner
0000036732
00036662
DNA
SEQ
-
-
1
Andreas Laner
0000036733
00036663
DNA
SEQ
-
-
1
Andreas Laner
0000036734
00036664
DNA
SEQ
-
-
1
Andreas Laner
0000036735
00036665
DNA
SEQ
-
-
1
Andreas Laner
0000036736
00036666
DNA
SEQ
-
-
1
Andreas Laner
0000036737
00036667
DNA
SEQ
-
-
1
Andreas Laner
0000036738
00036668
DNA
SEQ
-
-
1
Andreas Laner
0000036739
00036669
DNA
SEQ
-
-
1
Andreas Laner
0000036740
00036670
DNA
SEQ
-
-
1
Andreas Laner
0000036741
00036671
DNA
SEQ
-
-
1
Andreas Laner
0000036742
00036672
DNA
SEQ
-
-
1
Andreas Laner
0000036743
00036673
DNA
SEQ
-
-
1
Andreas Laner
0000036744
00036674
DNA
SEQ
-
-
1
Andreas Laner
0000036745
00036675
DNA
SEQ
-
-
1
Andreas Laner
0000036746
00036676
DNA
SEQ
-
-
1
Andreas Laner
0000036747
00036677
DNA
SEQ
-
-
1
Andreas Laner
0000047419
00047320
DNA
SEQ
-
-
1
James Whitworth
0000047982
00047856
DNA
SEQ
-
-
2
James Whitworth
0000047983
00047857
DNA
SEQ
-
-
2
James Whitworth
0000047984
00047858
DNA
SEQ
-
-
2
James Whitworth
0000047985
00047859
DNA
SEQ
-
-
2
James Whitworth
0000047997
00047871
DNA
SEQ
-
-
2
James Whitworth
0000104417
00103956
DNA
SEQ
-
-
1
Shahida Flores
0000104420
00103957
DNA
SEQ
-
-
1
Shahida Flores
0000104421
00103958
DNA
PCR;SEQ
-
-
1
Shahida Flores
0000223902
00222830
DNA
SEQ
-
-
1
Man Ting So
0000223903
00222831
DNA
SEQ
-
-
1
Man Ting So
0000223904
00222832
DNA
SEQ
-
-
1
Man Ting So
0000223905
00222833
?
?
-
-
1
LOVD
0000223906
00222834
?
?
-
-
1
LOVD
0000223907
00222835
?
?
-
-
1
LOVD
0000223908
00222836
?
?
-
-
1
LOVD
0000223909
00222837
?
?
-
-
1
LOVD
0000223910
00222838
?
?
-
-
1
LOVD
0000223911
00222839
?
?
-
-
1
LOVD
0000223912
00222840
?
?
-
-
1
LOVD
0000223913
00222841
?
?
-
-
1
LOVD
0000223914
00222842
?
?
-
-
1
LOVD
0000223915
00222843
?
?
-
-
1
LOVD
0000223916
00222844
?
?
-
-
1
LOVD
0000223917
00222845
?
?
-
-
1
LOVD
0000223918
00222846
?
?
-
-
1
LOVD
0000223919
00222847
?
?
-
-
1
LOVD
0000223920
00222848
?
?
-
-
1
LOVD
0000223921
00222849
?
?
-
-
1
LOVD
0000223922
00222850
?
?
-
-
1
LOVD
0000223923
00222851
?
?
-
-
1
LOVD
0000223924
00222852
?
?
-
-
1
LOVD
0000223925
00222853
?
?
-
-
1
LOVD
0000223926
00222854
DNA
SEQ
-
-
1
Man Ting So
0000223927
00222855
DNA
SEQ
-
-
1
Man Ting So
0000308229
00307087
DNA
SEQ-NG
-
WES
1
A. Arteche-López
0000309875
00308730
DNA
SEQ;SEQ-NG
-
105 WGS/200 WES
1
Global Variome, with Curator vacancy
0000317330
00316148
DNA
SEQ;SEQ-NG
-
330-gene panel
1
Johan den Dunnen
0000317332
00316150
DNA
SEQ;SEQ-NG
-
330-gene panel
2
Johan den Dunnen
0000317362
00316180
DNA
SEQ;SEQ-NG
-
330-gene panel
1
Johan den Dunnen
0000317367
00316185
DNA
SEQ;SEQ-NG
-
330-gene panel
1
Johan den Dunnen
0000373259
00372031
DNA
MLPA
-
NGS gene panel (SDHx, TMEM127, MAX, FH, RET, VHL)
1
Luigi Mori
0000398088
00396847
DNA
SEQ
-
-
1
Johan den Dunnen
0000398089
00396848
DNA
SEQ
-
-
1
Johan den Dunnen
0000398090
00396849
DNA
SEQ
-
-
1
Johan den Dunnen
0000398091
00396850
DNA
SEQ
-
-
1
Johan den Dunnen
0000398092
00396851
DNA
SEQ
-
-
1
Johan den Dunnen
0000398093
00396852
DNA
SEQ
-
-
1
Johan den Dunnen
0000398094
00396853
DNA
SEQ
-
-
1
Johan den Dunnen
0000398095
00396854
DNA
SEQ
-
-
1
Johan den Dunnen
0000398096
00396855
DNA
SEQ
-
-
1
Johan den Dunnen
0000398097
00396856
DNA
SEQ
-
-
1
Johan den Dunnen
0000398098
00396857
DNA
SEQ
-
-
1
Johan den Dunnen
0000437875
00436393
DNA
SEQ;SEQ-NG-I
PBMC
-
1
Anikó Bozsik
0000461928
00460296
DNA
SEQ-NG-I
-
-
1
Sarah Collis
0000467679
00466028
DNA
SEQ
-
-
1
Gemeinschaftspraxis für Humangenetik Dresden
10 per page
25 per page
50 per page
100 per page
Legend
How to query
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our
APIs
to retrieve data.
Powered by
LOVD v.3.0
Build 30b
LOVD software ©2004-2024
Leiden University Medical Center
Database contents © by their respective submitters and curators