Global Variome shared LOVD
FSCN2 (fascin homolog 2, actin-bundling protein, re...)
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Curator:
Global Variome, with Curator vacancy
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View FSCN2 gene homepage
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View all transcripts of gene FSCN2
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View all diseases associated with gene FSCN2
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All screenings for gene FSCN2
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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.
41 entries on 1 page. Showing entries 1 - 41.
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Legend
How to query
Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000171732
00170850
DNA
SEQ-NG-I
-
Gene Panel (79 IRD genes)
2
María González-del Pozo
0000234576
00233477
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234577
00233478
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234578
00233479
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234579
00233480
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234580
00233481
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234581
00233482
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234582
00233483
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234583
00233484
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234584
00233485
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234585
00233486
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234586
00233487
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234587
00233488
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234588
00233489
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234589
00233490
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234590
00233491
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234591
00233492
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234592
00233493
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234593
00233494
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234594
00233495
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234595
00233496
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234596
00233497
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234897
00233798
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000309562
00308418
DNA
SEQ;SEQ-NG
-
123 gene panel
1
Global Variome, with Curator vacancy
0000310814
00309669
DNA
SEQ;SEQ-NG
-
WES
1
Johan den Dunnen
0000321225
00320041
DNA
SEQ
-
-
1
Julia Lopez
0000327900
00326687
DNA
DHPLC
blood
-
1
Julia Lopez
0000335647
00334418
DNA
SEQ-NG
-
WES
1
LOVD
0000335788
00334559
DNA
SEQ-NG
-
WES
1
LOVD
0000336532
00335303
DNA
SEQ-NG
-
68-gene panel
1
Nereida Bravo Gil
0000336866
00335638
DNA
SEQ
-
-
1
Julia Lopez
0000336867
00335639
DNA
SEQ
-
-
1
Julia Lopez
0000336868
00335640
DNA
SEQ
-
-
1
Julia Lopez
0000336869
00335641
DNA
SEQ
-
-
1
Julia Lopez
0000336870
00335642
DNA
SEQ
-
-
1
Julia Lopez
0000337205
00335975
DNA
SEQ-NG
-
gene panel
1
LOVD
0000374714
00373479
DNA
SEQ-NG
-
73-gene panel
1
LOVD
0000382839
00381623
DNA
SEQ-NG-I;SEQ-NG-R;SEQ
blood
-
2
LOVD
0000382899
00381683
DNA
SEQ-NG-I;SEQ-NG-R;SEQ
blood
-
1
LOVD
0000383849
00382635
DNA
SEQ-NG
blood
unsolved
2
LOVD
0000389742
00388501
DNA
SEQ-NG
-
CNV gene panel next-generation sequencing
1
LOVD
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