Global Variome shared LOVD
CNGA1 (cyclic nucleotide gated channel alpha 1)
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Global Variome, with Curator vacancy
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All screenings for gene CNGA1
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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.
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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'
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146 entries on 2 pages. Showing entries 1 - 100.
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Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000096350
00095947
DNA
SEQ
WBC
-
1
James Hejtmancik
0000156284
00155419
DNA
SEQ
-
-
2
Dror Sharon
0000233679
00232580
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233680
00232581
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233681
00232582
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233682
00232583
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233683
00232584
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233684
00232585
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233685
00232586
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233686
00232587
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233687
00232588
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233688
00232589
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233689
00232590
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233690
00232591
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233691
00232592
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233692
00232593
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233693
00232594
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233694
00232595
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233695
00232596
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233696
00232597
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233697
00232598
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233698
00232599
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233699
00232600
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233700
00232601
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233701
00232602
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233702
00232603
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233703
00232604
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233704
00232605
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234775
00233676
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234776
00233677
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234777
00233678
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000309639
00308494
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310201
00309056
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310202
00309057
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310203
00309058
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310204
00309059
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310205
00309060
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310206
00309061
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310207
00309062
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310208
00309063
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000329330
00328115
DNA
SEQ-NG
-
WGS
2
LOVD
0000329546
00328331
DNA
SEQ-NG
-
WGS
1
LOVD
0000332496
00331276
DNA
SEQ;SEQ-NG
-
39-gene panel
2
LOVD
0000332920
00331701
DNA
SEQ-NG
-
-
2
LOVD
0000332921
00331702
DNA
SEQ-NG
-
-
1
LOVD
0000333752
00332528
DNA
SEQ-NG
-
gene panel
2
LOVD
0000336629
00335400
DNA
SEQ-NG
-
283-gene panel
1
LOVD
0000363400
00362171
DNA
SEQ-NG
-
gene panel
2
LOVD
0000364739
00363511
DNA
SEQ-NG
-
gene panel
1
LOVD
0000364740
00363512
DNA
SEQ-NG
-
gene panel
1
LOVD
0000374647
00373412
DNA
arraySNP;SEQ
-
-
1
LOVD
0000374740
00373505
DNA
SEQ-NG
-
316-gene panel
2
LOVD
0000375042
00373810
DNA
arraySEQ
-
Reseq
1
LOVD
0000376525
00375328
DNA
SEQ-NG
-
193-gene panel
1
LOVD
0000376526
00375329
DNA
SEQ-NG
-
193-gene panel
2
LOVD
0000376527
00375330
DNA
SEQ-NG
-
193-gene panel
1
LOVD
0000377383
00376187
DNA
DHPLC
blood
-
1
LOVD
0000377721
00376516
DNA
PCRm;SEQ
blood
-
1
LOVD
0000378423
00377218
DNA
SEQ-NG-I;SEQ
blood
targeted resequencing using MIPs library prep; 108-gene panel
1
LOVD
0000378704
00377501
DNA
?
-
various screening techniques within publication, not mentioned which particular individual had which techniques: SSCA, DGGE, arraySNP, SEQ-NG, WES
2
LOVD
0000379019
00377815
DNA
PE
blood
-
3
LOVD
0000379040
00377836
DNA
PE
blood
-
1
LOVD
0000379041
00377837
DNA
PE
blood
-
2
LOVD
0000379042
00377838
DNA
PE
blood
-
1
LOVD
0000381022
00379820
DNA
SEQ-NG
-
panel of 441 hereditary eye disease genes including 291 genes related to IRD
1
LOVD
0000381411
00380209
DNA
SEQ-NG
blood
-
2
LOVD
0000381412
00380210
DNA
SEQ-NG
blood
-
2
LOVD
0000382229
00381015
DNA
arraySEQ;SEQ;PCR
blood
-
1
LOVD
0000382837
00381621
DNA
SEQ-NG-I;SEQ-NG-R;SEQ
blood
-
3
LOVD
0000382851
00381635
DNA
SEQ-NG-I;SEQ-NG-R;SEQ
blood
-
2
LOVD
0000382929
00381713
DNA
PCR;SEQ-NG
blood or a saliva sample
-
2
LOVD
0000383097
00381881
DNA
SEQ-NG
blood
-
2
LOVD
0000383733
00382519
DNA
SEQ-NG-I
blood
125 genes associated with inherited retinal disorders, see paper supplemental data
1
LOVD
0000383734
00382520
DNA
SEQ-NG-I
blood
125 genes associated with inherited retinal disorders, see paper supplemental data
2
LOVD
0000383735
00382521
DNA
SEQ-NG-I
blood
125 genes associated with inherited retinal disorders, see paper supplemental data
1
LOVD
0000384971
00383746
DNA
SEQ-NG
-
-
1
LOVD
0000385030
00383805
DNA
SEQ-NG
-
-
1
LOVD
0000385191
00383966
DNA
arraySNP
-
-
1
LOVD
0000385237
00384012
DNA
SEQ-NG-I
-
-
1
LOVD
0000385238
00384013
DNA
arraySNP
-
-
1
LOVD
0000385282
00384057
DNA
arraySNP
-
-
1
LOVD
0000385294
00384069
DNA
arraySNP
-
-
1
LOVD
0000385322
00384097
DNA
SEQ-NG-I
-
-
2
LOVD
0000385330
00384105
DNA
SEQ-NG-I
-
-
1
LOVD
0000385965
00384739
DNA
arraySEQ;MLPA
-
-
1
LOVD
0000385977
00384751
DNA
arraySEQ;MLPA
-
-
1
LOVD
0000385978
00384752
DNA
arraySEQ;MLPA
-
-
1
LOVD
0000385979
00384753
DNA
arraySEQ;MLPA
-
-
1
LOVD
0000386932
00385704
DNA
SEQ-NG
blood
Panel 3 containing 78 genes
2
LOVD
0000386940
00385712
DNA
SEQ-NG
blood
Panel 4 containing 370 genes
1
LOVD
0000387843
00386615
DNA
SEQ-NG-I;SEQ
blood
-
2
LOVD
0000387848
00386620
DNA
SEQ-NG-I;SEQ
blood
-
2
LOVD
0000387861
00386633
DNA
SEQ-NG-I;SEQ
blood
-
2
LOVD
0000390037
00388794
DNA
SEQ-NG
blood
RET3 targeted sequencing panel - see paper
2
LOVD
0000390687
00389444
DNA
SEQ-NG
blood
RET7 targeted sequencing panel - see paper
1
LOVD
0000390906
00389663
DNA
SEQ-NG
blood
RET7 targeted sequencing panel - see paper
1
LOVD
0000391098
00389855
DNA
SEQ-NG
blood
RET3 targeted sequencing panel - see paper
1
LOVD
0000391126
00389883
DNA
SEQ-NG
blood
RET7 targeted sequencing panel - see paper
2
LOVD
0000391128
00389885
DNA
SEQ-NG
blood
RET7 targeted sequencing panel - see paper
1
LOVD
0000391462
00390221
DNA
SEQ-NG-I
blood
whole genome sequencing
2
LOVD
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