Global Variome shared LOVD
EFTUD2 (elongation factor Tu GTP binding domain con...)
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Curator:
Dennis E. Bulman
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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
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.
66 entries on 1 page. Showing entries 1 - 66.
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Legend
How to query
Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000001434
00001634
DNA
SEQ
-
-
1
Johan den Dunnen
0000001435
00001635
DNA
SEQ
-
-
1
Johan den Dunnen
0000002292
00002418
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002293
00002419
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002294
00002420
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002295
00002421
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002296
00002422
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002297
00002423
DNA
SEQ;SEQ-NG-I
-
-
1
Dennis E. Bulman
0000002301
00002427
DNA
arrayCGH
-
-
1
Dennis E. Bulman
0000002302
00002428
DNA
arraySNP
-
-
1
Dennis E. Bulman
0000002303
00002429
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002304
00002430
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002309
00002433
DNA
arrayCGH;SEQ
-
-
1
Dennis E. Bulman
0000002310
00002434
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002312
00002436
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002313
00002437
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002314
00002438
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002315
00002439
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002316
00002442
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002317
00002443
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002326
00002452
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002327
00002453
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002328
00002456
DNA
SEQ;SEQ-NG-I
-
-
1
Dennis E. Bulman
0000002480
00002604
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002499
00002622
DNA
SEQ
-
-
1
Dennis E. Bulman
0000002509
00002629
DNA
SEQ
-
-
1
Dennis E. Bulman
0000004057
00004131
DNA
SEQ
-
-
1
Christopher Gordon
0000004058
00004132
DNA
SEQ
-
-
1
Christopher Gordon
0000004059
00004133
DNA
SEQ
-
-
1
Christopher Gordon
0000004060
00004134
DNA
SEQ
-
-
1
Christopher Gordon
0000004061
00004135
DNA
SEQ
-
-
1
Christopher Gordon
0000004062
00004136
DNA
SEQ
-
-
Not yet submitted
Christopher Gordon
0000004063
00004137
DNA
SEQ
-
-
1
Christopher Gordon
0000004064
00004138
DNA
SEQ
-
-
1
Christopher Gordon
0000004065
00004139
DNA
SEQ
-
-
1
Christopher Gordon
0000004066
00004140
DNA
SEQ
-
-
1
Christopher Gordon
0000004067
00004141
DNA
SEQ
-
-
1
Christopher Gordon
0000004068
00004136
DNA
SEQ
-
-
1
Christopher Gordon
0000004069
00004142
DNA
SEQ
-
-
1
Christopher Gordon
0000004070
00004143
DNA
SEQ
-
-
1
Christopher Gordon
0000004071
00004144
DNA
SEQ
-
-
1
Christopher Gordon
0000004072
00004145
DNA
SEQ
-
-
1
Christopher Gordon
0000004073
00004146
DNA
SEQ
-
-
1
Christopher Gordon
0000004074
00004147
DNA
SEQ
-
-
1
Christopher Gordon
0000004075
00004148
DNA
SEQ
-
-
1
Christopher Gordon
0000004076
00004149
DNA
SEQ
-
-
1
Christopher Gordon
0000004077
00004150
DNA
SEQ
-
-
1
Christopher Gordon
0000004078
00004151
DNA
SEQ
-
-
1
Christopher Gordon
0000004079
00004152
DNA
SEQ
-
-
1
Christopher Gordon
0000004080
00004153
DNA
SEQ
-
-
1
Christopher Gordon
0000004081
00004154
DNA
SEQ
-
-
1
Christopher Gordon
0000011375
00011460
DNA
SEQ;SEQ-NG-I
-
-
1
Dennis E. Bulman
0000011376
00011461
DNA
SEQ;SEQ-NG-I
-
-
1
Dennis E. Bulman
0000039064
00038826
DNA
SEQ
-
-
1
Dennis E. Bulman
0000046436
00046331
DNA
arrayCGH
-
-
1
Dennis E. Bulman
0000050446
00050501
DNA
SEQ;SEQ-NG-I
-
-
1
Johan den Dunnen
0000105044
00104572
DNA
SEQ-NG-I
blood
-
1
Jana Paderova
0000181055
00180152
DNA
SEQ-NG
-
WES
1
Johan den Dunnen
0000290528
00289358
DNA
SEQ-NG-I
-
-
1
So Young Kim
0000296843
00295671
DNA
?
-
-
1
Huw Thomas
0000296844
00295672
DNA
?
-
-
1
Huw Thomas
0000296845
00295673
DNA
?
-
-
1
Huw Thomas
0000296847
00295675
DNA
?
-
-
1
Huw Thomas
0000296848
00295676
DNA
?
-
-
1
Huw Thomas
0000307347
00306214
DNA
SEQ-NG
-
-
1
Sha Hong
0000465996
00464365
DNA;RNA
RT-PCR;SEQ;SEQ-NG
Blood
The variant was initially identified using Whole Exome Sequencing (WES) and confirmed by Sanger sequencing.RNA sequencing (RNA-seq) confirmed exon 6 skipping due to c.492+1del mutation.
1
Ying Xu
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