Global Variome shared LOVD
EDNRB (endothelin receptor type B)
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
Curator:
Veronique Pingault
View all genes
View EDNRB gene homepage
View graphs about the EDNRB gene database
Create a new gene entry
View all transcripts
View all transcripts of gene EDNRB
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene EDNRB
View all variants in gene EDNRB
Full data view for gene EDNRB
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 EDNRB
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene EDNRB
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene EDNRB
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
All screenings for gene EDNRB
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.
77 entries on 1 page. Showing entries 1 - 77.
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
0000089182
00089039
DNA
SEQ
-
-
1
Gemeinschaftspraxis für Humangenetik Dresden
0000286111
00284961
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286112
00284962
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286114
00284964
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286116
00284966
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286117
00284967
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286118
00284968
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286119
00284969
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286120
00284970
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286121
00284971
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286124
00284974
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286125
00284975
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286126
00284976
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286127
00284977
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286128
00284978
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286131
00284981
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286132
00284982
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286133
00284983
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286135
00284985
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286137
00284987
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286138
00284988
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286139
00284989
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286140
00284990
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286142
00284992
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286145
00284995
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286146
00284996
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286148
00284998
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286150
00285000
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286151
00285001
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286152
00285002
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286153
00285003
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286154
00285004
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286155
00285005
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286156
00285006
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286157
00285007
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286158
00285008
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286159
00285009
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286160
00285010
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000286162
00285012
DNA
?
-
-
1
Global Variome, with Curator vacancy
0000308229
00307087
DNA
SEQ-NG
-
WES
1
A. Arteche-López
0000316703
00315523
DNA
?
-
-
1
Veronique Pingault
0000316704
00315524
DNA
?
-
-
1
Veronique Pingault
0000316705
00315525
DNA
?
-
-
1
Veronique Pingault
0000316706
00315526
DNA
DGGE;SSCA;SEQ
-
-
1
Veronique Pingault
0000316707
00315527
DNA
SSCA;SEQ
-
-
1
Veronique Pingault
0000316708
00315528
DNA
?
-
-
1
Veronique Pingault
0000316709
00315529
DNA
?
-
-
1
Veronique Pingault
0000316710
00315530
DNA
SEQ
-
-
1
Veronique Pingault
0000316711
00315531
DNA
SEQ
-
-
2
Veronique Pingault
0000316712
00315532
DNA
SSCA;SEQ
-
-
1
Veronique Pingault
0000316713
00315533
DNA
SEQ
-
-
1
Veronique Pingault
0000316714
00315534
DNA
SEQ
-
-
1
Veronique Pingault
0000316715
00315535
DNA
SSCA;SEQ
-
-
1
Veronique Pingault
0000316716
00315536
DNA
SEQ
-
-
2
Veronique Pingault
0000316717
00315537
DNA
DGGE;SEQ
-
-
1
Veronique Pingault
0000316718
00315538
DNA
SEQ
-
-
1
Veronique Pingault
0000316719
00315539
DNA
SEQ
-
-
1
Veronique Pingault
0000316720
00315540
DNA
?
-
-
1
Veronique Pingault
0000316721
00315541
DNA
SSCA;SEQ
-
-
1
Veronique Pingault
0000316722
00315542
DNA
SEQ
-
-
2
Veronique Pingault
0000316723
00315543
DNA
SEQ
-
-
1
Veronique Pingault
0000316724
00315544
DNA
SSCA;SEQ
-
-
1
Veronique Pingault
0000316725
00315545
DNA
SEQ
-
-
1
Veronique Pingault
0000316726
00315546
DNA
SEQ
-
-
1
Veronique Pingault
0000316727
00315547
DNA
SSCA;SEQ
-
-
1
Veronique Pingault
0000316728
00315548
DNA
PCRq
-
-
2
Veronique Pingault
0000316729
00315549
DNA
SEQ
-
-
1
Veronique Pingault
0000316730
00315550
DNA
SEQ
-
-
1
Veronique Pingault
0000316731
00315551
DNA
SEQ
-
-
1
Veronique Pingault
0000316732
00315552
DNA
microscope;arrayCGH
lymphocytes
-
1
Veronique Pingault
0000316733
00315553
DNA
microscope;arrayCGH
lymphocytes
-
1
Veronique Pingault
0000316734
00315554
DNA
FISH
lymphocytes
-
1
Veronique Pingault
0000316735
00315555
DNA
FISH
lymphocytes
-
1
Veronique Pingault
0000316736
00315556
DNA
FISH
lymphocytes
-
1
Veronique Pingault
0000316737
00315557
DNA
arrayCGH;SEQ
-
-
2
Veronique Pingault
0000316738
00315558
DNA
SEQ
-
-
2
Veronique Pingault
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