Global Variome shared LOVD
KCNV2 (potassium channel, subfamily V, member 2)
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Curator:
Global Variome, with Curator vacancy
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All screenings for gene KCNV2
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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
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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.
291 entries on 3 pages. Showing entries 1 - 100.
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How to query
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Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000156349
00155484
DNA
SEQ
-
-
1
Dror Sharon
0000156350
00155485
DNA
SEQ
-
-
1
Dror Sharon
0000156351
00155486
DNA
SEQ
-
-
2
Dror Sharon
0000156352
00155487
DNA
SEQ
-
-
1
Dror Sharon
0000156353
00155488
DNA
SEQ
-
-
2
Dror Sharon
0000156354
00155489
DNA
SEQ
-
-
1
Dror Sharon
0000309757
00308612
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000309869
00308724
DNA
SEQ;SEQ-NG
-
105 WGS/200 WES
1
Global Variome, with Curator vacancy
0000310348
00309203
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310349
00309204
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310350
00309205
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310351
00309206
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310352
00309207
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310353
00309208
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310354
00309209
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310355
00309210
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000326682
00325471
DNA
SEQ;SEQ-NG
-
199 gene panel
1
Johan den Dunnen
0000329319
00328104
DNA
SEQ-NG
-
WGS
2
LOVD
0000329512
00328297
DNA
SEQ-NG
-
WGS
2
LOVD
0000329674
00328459
DNA
SEQ-NG
-
gene panel
1
LOVD
0000335215
00333989
DNA
SEQ-NG
-
-
1
LOVD
0000335216
00333990
DNA
SEQ-NG
-
-
1
LOVD
0000335686
00334457
DNA
SEQ-NG
-
WES
2
LOVD
0000363376
00362147
DNA
SEQ-NG
-
WES
1
Johan den Dunnen
0000363396
00362167
DNA
SEQ-NG
-
gene panel
2
LOVD
0000364824
00363596
DNA
SEQ-NG
-
gene panel
1
LOVD
0000364841
00363613
DNA
SEQ-NG
-
gene panel
1
LOVD
0000364864
00363636
DNA
SEQ-NG
-
gene panel
1
LOVD
0000364897
00363669
DNA
SEQ-NG
-
gene panel
1
LOVD
0000364957
00363729
DNA
SEQ-NG
-
gene panel
1
LOVD
0000364958
00363730
DNA
SEQ-NG
-
gene panel
1
LOVD
0000373744
00372511
DNA
SEQ-NG
-
163-gene panel
2
LOVD
0000379009
00377805
DNA
SEQ
-
-
1
LOVD
0000379194
00377990
DNA
PCR; SEQ
blood
-
1
LOVD
0000379195
00377991
DNA
PCR; SEQ
blood
-
1
LOVD
0000379197
00377993
DNA
PCR; SEQ
blood
-
1
LOVD
0000379198
00377994
DNA
PCR; SEQ
blood
-
1
LOVD
0000379199
00377995
DNA
PCR; SEQ
blood
-
1
LOVD
0000379200
00377996
DNA
PCR; SEQ
blood
-
1
LOVD
0000379201
00377997
DNA
PCR; SEQ
blood
-
1
LOVD
0000379202
00377998
DNA
PCR; SEQ
blood
-
1
LOVD
0000379203
00377999
DNA
PCR; SEQ
blood
-
1
LOVD
0000379204
00378000
DNA
PCR; SEQ
blood
-
1
LOVD
0000379205
00378001
DNA
PCR; SEQ
blood
-
1
LOVD
0000379206
00378002
DNA
PCR; SEQ
blood
-
1
LOVD
0000379207
00378003
DNA
PCR; SEQ
blood
-
1
LOVD
0000379208
00378004
DNA
PCR; SEQ
blood
-
1
LOVD
0000381503
00380289
DNA
SEQ-NG
blood
autozygome-guided sequencing
1
LOVD
0000381504
00380290
DNA
SEQ-NG
blood
autozygome-guided sequencing
1
LOVD
0000381505
00380291
DNA
SEQ-NG
blood
autozygome-guided sequencing
1
LOVD
0000381506
00380292
DNA
SEQ-NG
blood
autozygome-guided sequencing
1
LOVD
0000381507
00380293
DNA
SEQ-NG
blood
autozygome-guided sequencing
1
LOVD
0000381508
00380294
DNA
SEQ-NG
blood
autozygome-guided sequencing
1
LOVD
0000381509
00380295
DNA
SEQ-NG
blood
autozygome-guided sequencing
1
LOVD
0000382792
00381576
DNA
SEQ
blood
-
1
LOVD
0000382793
00381577
DNA
SEQ
blood
-
2
LOVD
0000382794
00381578
DNA
SEQ
blood
-
2
LOVD
0000382795
00381579
DNA
SEQ
blood
-
1
LOVD
0000382796
00381580
DNA
SEQ
blood
-
1
LOVD
0000382797
00381581
DNA
SEQ
blood
-
1
LOVD
0000382798
00381582
DNA
SEQ
blood
-
1
LOVD
0000382799
00381583
DNA
SEQ
blood
-
1
LOVD
0000382800
00381584
DNA
SEQ
blood
-
1
LOVD
0000382801
00381585
DNA
SEQ
blood
-
1
LOVD
0000382802
00381586
DNA
SEQ
blood
-
1
LOVD
0000382803
00381587
DNA
SEQ
blood
-
1
LOVD
0000382804
00381588
DNA
SEQ
blood
-
2
LOVD
0000382805
00381589
DNA
SEQ
blood
-
1
LOVD
0000382806
00381590
DNA
SEQ
blood
-
2
LOVD
0000382807
00381591
DNA
SEQ
blood
-
1
LOVD
0000382808
00381592
DNA
SEQ
blood
-
2
LOVD
0000382809
00381593
DNA
SEQ
blood
-
1
LOVD
0000383772
00382558
DNA
SEQ-NG-I
blood
125 genes associated with inherited retinal disorders, see paper supplemental data
1
LOVD
0000383773
00382559
DNA
SEQ-NG-I
blood
125 genes associated with inherited retinal disorders, see paper supplemental data
1
LOVD
0000384019
00382803
DNA
arraySEQ;PCR
blood
-
2
LOVD
0000384660
00383435
DNA
?
-
retrospective study
1
LOVD
0000384661
00383436
DNA
?
-
retrospective study
1
LOVD
0000384662
00383437
DNA
?
-
retrospective study
1
LOVD
0000384663
00383438
DNA
?
-
retrospective study
1
LOVD
0000384664
00383439
DNA
?
-
retrospective study
1
LOVD
0000384665
00383440
DNA
?
-
retrospective study
1
LOVD
0000384666
00383441
DNA
?
-
retrospective study
1
LOVD
0000384667
00383442
DNA
?
-
retrospective study
1
LOVD
0000385367
00384142
DNA
SEQ-NG-I
-
-
2
LOVD
0000385655
00384430
DNA
SEQ-NG
blood
panel of 126 genes
2
LOVD
0000390920
00389677
DNA
SEQ-NG
blood
RET2 targeted sequencing panel - see paper
1
LOVD
0000390982
00389739
DNA
SEQ-NG
blood
RET5 targeted sequencing panel - see paper
1
LOVD
0000390984
00389741
DNA
SEQ-NG
blood
RET6 targeted sequencing panel - see paper
2
LOVD
0000390993
00389750
DNA
SEQ-NG
blood
RET9 targeted sequencing panel - see paper
2
LOVD
0000391534
00390293
DNA
SEQ-NG-I
blood
whole genome sequencing
2
LOVD
0000392069
00390828
DNA
?
-
-
4
LOVD
0000392098
00390857
DNA
SEQ
-
-
2
LOVD
0000392169
00390928
DNA
SEQ
-
-
2
LOVD
0000392415
00391173
DNA
SEQ-NG-I
blood
whole exome sequencing
2
LOVD
0000392609
00391367
DNA
SEQ-NG
-
retrospective case note review, targeted gene panel testing
1
LOVD
0000392800
00391558
DNA
?
blood
NGS gene panel investigation in 60 families, Sanger sequencing in 27 families, and Asper microarray in 25 families
1
LOVD
0000392801
00391559
DNA
?
blood
NGS gene panel investigation in 60 families, Sanger sequencing in 27 families, and Asper microarray in 25 families
1
LOVD
0000394938
00393690
DNA
SEQ-NG
-
hereditary eye disease enrichment panel (HEDEP)
2
LOVD
0000397002
00395763
DNA
SEQ-NG
blood
212 inherited retinal disease-related genes
2
LOVD
0000416451
00415170
DNA
SEQ
blood
-
2
LOVD
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