Global Variome shared LOVD
SEMA4A (sema domain, immunoglobulin domain (Ig), tr...)
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Curator:
Global Variome, with Curator vacancy
View all genes
View SEMA4A gene homepage
View graphs about the SEMA4A gene database
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View all transcripts
View all transcripts of gene SEMA4A
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View all variants
View all variants affecting transcripts
View unique variants in gene SEMA4A
View all variants in gene SEMA4A
Full data view for gene SEMA4A
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View active genomic custom columns
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View all individuals with variants in gene SEMA4A
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View all diseases
View all diseases associated with gene SEMA4A
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View available phenotype columns
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View all screenings for gene SEMA4A
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All screenings for gene SEMA4A
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.
53 entries on 1 page. Showing entries 1 - 53.
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Legend
How to query
Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000033159
00033091
DNA
SEQ;SEQ-NG-S
-
-
6
Kornelia Neveling
0000033161
00033093
DNA
SEQ;SEQ-NG-S
-
-
5
Kornelia Neveling
0000033165
00033097
DNA
SEQ;SEQ-NG-S
-
-
1
Kornelia Neveling
0000033174
00033106
DNA
SEQ;SEQ-NG-S
-
-
3
Kornelia Neveling
0000033178
00033110
DNA
SEQ;SEQ-NG-S
-
-
1
Kornelia Neveling
0000033185
00033117
DNA
SEQ;SEQ-NG-S
-
-
1
Kornelia Neveling
0000033193
00033125
DNA
SEQ;SEQ-NG-S
-
-
4
Kornelia Neveling
0000033203
00033135
DNA
SEQ;SEQ-NG-S
-
-
2
Kornelia Neveling
0000033206
00033138
DNA
SEQ;SEQ-NG-S
-
-
7
Kornelia Neveling
0000033211
00033143
DNA
SEQ;SEQ-NG-S
-
-
3
Kornelia Neveling
0000033212
00033144
DNA
SEQ;SEQ-NG-S
-
-
5
Kornelia Neveling
0000033216
00033148
DNA
SEQ;SEQ-NG-S
-
-
2
Kornelia Neveling
0000033217
00033149
DNA
SEQ;SEQ-NG-S
-
-
1
Kornelia Neveling
0000033221
00033153
DNA
SEQ;SEQ-NG-S
-
-
3
Kornelia Neveling
0000033232
00033164
DNA
SEQ;SEQ-NG-S
-
-
1
Kornelia Neveling
0000033435
00033367
DNA
SSCA;SEQ;PCR;PAGE
-
-
1
Raheel Qamar
0000033436
00033368
DNA
SSCA;SEQ;PCR;PAGE
-
-
1
Raheel Qamar
0000033437
00033369
DNA
SSCA;SEQ;PCR;PAGE
-
-
2
Raheel Qamar
0000033438
00033370
DNA
SSCA;SEQ;PCR;PAGE
-
-
2
Raheel Qamar
0000033439
00033371
DNA
SSCA;SEQ;PCR;PAGE
-
-
2
Raheel Qamar
0000033440
00033372
DNA
SSCA;SEQ;PCR;PAGE
-
-
2
Raheel Qamar
0000033441
00033373
DNA
SSCA;SEQ;PCR;PAGE
-
-
1
Raheel Qamar
0000033442
00033374
DNA
SSCA;SEQ;PCR;PAGE
-
-
1
Raheel Qamar
0000033443
00033375
DNA
SSCA;SEQ;PCR;PAGE
-
-
1
Raheel Qamar
0000033444
00033376
DNA
SSCA;SEQ;PCR;PAGE
-
-
1
Raheel Qamar
0000033445
00033377
DNA
SSCA;SEQ;PCR;PAGE
-
-
1
Raheel Qamar
0000033446
00033378
DNA
SSCA;SEQ;PCR;PAGE
-
-
1
Raheel Qamar
0000233081
00231982
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233082
00231983
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233083
00231984
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233084
00231985
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233085
00231986
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233086
00231987
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233087
00231988
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233088
00231989
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233089
00231990
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000233090
00231991
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000234701
00233602
DNA
SEQ-NG
-
-
1
Yoshito Koyanagi
0000277237
00276092
DNA
PCR
blood
-
1
Mariona Terradas
0000277239
00276094
DNA
PCR
blood
-
1
Mariona Terradas
0000309523
00308379
DNA
SEQ;SEQ-NG
-
123 gene panel
1
Global Variome, with Curator vacancy
0000309524
00308380
DNA
SEQ;SEQ-NG
-
123 gene panel
1
Global Variome, with Curator vacancy
0000329633
00328419
DNA
SEQ-NG
-
WES
1
LOVD
0000333269
00332050
DNA
SEQ-NG
-
-
1
LOVD
0000380631
00379431
DNA
SEQ
blood
WES
1
LOVD
0000380914
00379712
DNA
SEQ-NG-I
blood
Whole-exome sequencing
1
LOVD
0000380915
00379713
DNA
SEQ-NG-I
blood
Whole-exome sequencing
1
LOVD
0000383033
00381817
DNA
PCR;SEQ-NG
blood or a saliva sample
-
1
LOVD
0000390403
00389160
DNA
SEQ-NG
blood
RET7 targeted sequencing panel - see paper
1
LOVD
0000390741
00389498
DNA
SEQ
blood
Sanger sequencing
1
LOVD
0000390742
00389499
DNA
SEQ-NG
blood
RET2 targeted sequencing panel - see paper
1
LOVD
0000390760
00389517
DNA
SEQ-NG
blood
RET3 targeted sequencing panel - see paper
1
LOVD
0000390863
00389620
DNA
SEQ-NG
blood
RET5 targeted sequencing panel - see paper
1
LOVD
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Legend
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