Global Variome shared LOVD
CNNM4 (cyclin M4)
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Curator:
Global Variome, with Curator vacancy
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View CNNM4 gene homepage
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View all transcripts of gene CNNM4
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View all variants affecting transcripts
View unique variants in gene CNNM4
View all variants in gene CNNM4
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View all individuals with variants in gene CNNM4
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View all diseases associated with gene CNNM4
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View available phenotype columns
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View all screenings for gene CNNM4
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All screenings for gene CNNM4
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
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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.
78 entries on 1 page. Showing entries 1 - 78.
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Legend
How to query
Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000059777
00059790
DNA
SEQ-NG-I
-
-
1
Leen Abu Safieh
0000156312
00155447
DNA
SEQ
-
-
1
Dror Sharon
0000156313
00155448
DNA
SEQ
-
-
1
Dror Sharon
0000310249
00309104
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310250
00309105
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000337200
00335970
DNA
SEQ-NG
-
gene panel
1
LOVD
0000364844
00363616
DNA
SEQ-NG
-
gene panel
1
LOVD
0000364886
00363658
DNA
SEQ-NG
-
gene panel
1
LOVD
0000365094
00363866
DNA
SEQ
-
-
1
Dror Sharon
0000373736
00372503
DNA
SEQ-NG
-
163-gene panel
1
LOVD
0000374742
00373507
DNA
SEQ-NG
-
316-gene panel
2
LOVD
0000383743
00382529
DNA
SEQ-NG-I
blood
125 genes associated with inherited retinal disorders, see paper supplemental data
1
LOVD
0000384645
00383420
DNA
?
-
retrospective study
1
LOVD
0000386281
00385052
DNA
SEQ-NG
-
targeted next-generation sequencing
2
LOVD
0000387110
00385882
DNA
SEQ;SEQ-NG
-
disease gene panel
1
Johan den Dunnen
0000387528
00386299
DNA
SEQ-NG-I
blood
-
2
LOVD
0000390925
00389682
DNA
SEQ-NG
blood
RET3 targeted sequencing panel - see paper
1
LOVD
0000395003
00393755
DNA
SEQ-NG
-
hereditary eye disease enrichment panel (HEDEP)
2
LOVD
0000414442
00413172
DNA
SEQ
-
-
1
LOVD
0000414443
00413173
DNA
SEQ
-
-
1
LOVD
0000414444
00413174
DNA
SEQ
-
-
1
LOVD
0000414445
00413175
DNA
SEQ
-
-
1
LOVD
0000414446
00413176
DNA
SEQ
-
-
1
LOVD
0000414447
00413177
DNA
SEQ
-
-
2
LOVD
0000414448
00413178
DNA
SEQ
-
-
2
LOVD
0000414449
00413179
DNA
SEQ
-
-
2
LOVD
0000414450
00413180
DNA
SEQ
-
-
2
LOVD
0000414451
00413181
DNA
SEQ
-
-
1
LOVD
0000414452
00413182
DNA
SEQ
-
-
1
LOVD
0000414453
00413183
DNA
SEQ
-
-
1
LOVD
0000414454
00413184
DNA
SEQ
-
-
1
LOVD
0000414455
00413185
DNA
SEQ
-
-
1
LOVD
0000414456
00413186
DNA
SEQ
-
-
1
LOVD
0000414457
00413187
DNA
SEQ
-
-
2
LOVD
0000414458
00413188
DNA
SEQ
-
-
1
LOVD
0000414459
00413189
DNA
arraySNP;SEQ
-
-
1
LOVD
0000414460
00413190
DNA
arraySNP;SEQ
-
-
1
LOVD
0000414469
00413199
DNA
arraySNP;SEQ
-
-
1
LOVD
0000414470
00413200
DNA
arraySNP;SEQ
-
-
1
LOVD
0000414471
00413201
DNA
arraySNP;SEQ
-
-
1
LOVD
0000414472
00413202
DNA
arraySNP;SEQ
-
-
1
LOVD
0000414473
00413203
DNA
?
-
clinical description retrospective study
1
LOVD
0000414474
00413204
DNA
?
-
clinical description retrospective study
1
LOVD
0000414475
00413205
DNA
?
-
clinical description retrospective study
1
LOVD
0000414479
00413208
DNA
SEQ
-
-
1
LOVD
0000414481
00413210
DNA
SEQ
-
-
1
LOVD
0000414482
00413211
DNA
SEQ
-
-
1
LOVD
0000414483
00413212
DNA
SEQ
-
-
1
LOVD
0000414484
00413213
DNA
SEQ
-
-
1
LOVD
0000414485
00413214
DNA
SEQ
blood
-
1
LOVD
0000414486
00413215
DNA
SEQ
blood
-
1
LOVD
0000414487
00413216
DNA
SEQ
blood
-
1
LOVD
0000414488
00413217
DNA
SEQ
blood
-
1
LOVD
0000414489
00413218
DNA
SEQ
blood
-
1
LOVD
0000414490
00413219
DNA
SEQ
blood
-
1
LOVD
0000414491
00413220
DNA
SEQ
blood
-
1
LOVD
0000414492
00413221
DNA
SEQ
blood
-
1
LOVD
0000414493
00413222
DNA
SEQ
blood
-
1
LOVD
0000414494
00413223
DNA
SEQ
blood
-
1
LOVD
0000414495
00413224
DNA
SEQ-NG;SEQ
blood
exome sequencing
1
LOVD
0000414496
00413225
DNA
SEQ
blood
exome sequencing
1
LOVD
0000414497
00413226
DNA
SEQ
blood
exome sequencing
1
LOVD
0000414498
00413227
DNA
STR;SEQ
blood
-
1
LOVD
0000414499
00413228
DNA
STR;SEQ
blood
-
1
LOVD
0000414500
00413229
DNA
STR;SEQ
blood
-
1
LOVD
0000414503
00413231
DNA
?
-
retrospective multicenter observational study
1
LOVD
0000414504
00413232
DNA
?
-
retrospective multicenter observational study
1
LOVD
0000414505
00413233
DNA
?
-
retrospective multicenter observational study
2
LOVD
0000414506
00413234
DNA
?
-
retrospective multicenter observational study
1
LOVD
0000414507
00413235
DNA
?
-
retrospective multicenter observational study
1
LOVD
0000414508
00413236
DNA
SEQ
buccal mucosa cells
-
1
LOVD
0000414509
00413237
DNA
SEQ
buccal mucosa cells
-
2
LOVD
0000414514
00413242
DNA
SEQ
blood
-
1
LOVD
0000414515
00413243
DNA
SEQ
blood
-
1
LOVD
0000414516
00413244
DNA
SEQ
blood
-
1
LOVD
0000422702
00421391
DNA
SEQ-NG;SEQ
-
581 gene panel from Molecular Vision Lab (MVL Panel v1)
1
LOVD
0000422703
00421392
DNA
SEQ-NG;SEQ
-
Molecular Vision Lab NGS Retinal Dystrophy SmartPanel v11 (281 genes)
1
LOVD
0000422704
00421393
DNA
SEQ-NG;SEQ
-
clinical whole exome sequencing
1
LOVD
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