Global Variome shared LOVD
DFNB31 (deafness, autosomal recessive 31)
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
Curator:
David Baux
View all genes
View DFNB31 gene homepage
View graphs about the DFNB31 gene database
Create a new gene entry
View all transcripts
View all transcripts of gene DFNB31
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene DFNB31
View all variants in gene DFNB31
Full data view for gene DFNB31
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
View all individuals with variants in gene DFNB31
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene DFNB31
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene DFNB31
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
All screenings for gene DFNB31
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.
113 entries on 2 pages. Showing entries 1 - 100.
10 per page
25 per page
50 per page
100 per page
Legend
How to query
« First
Prev
1
2
Next
Last »
Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000059110
00059139
DNA
SEQ;SEQ-NG-I
-
-
1
Manou Sommen
0000164139
00163274
DNA
SEQ
-
-
12
Anne-Françoise Roux
0000164140
00163275
DNA
SEQ
-
-
6
Anne-Françoise Roux
0000164141
00163276
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164142
00163277
DNA
SEQ;SSCA
-
-
1
Jose Maria Millan
0000164143
00163278
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164144
00163279
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164145
00163280
DNA
SEQ;SEQ-NG-S
-
-
5
Anne-Françoise Roux
0000164146
00163281
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164147
00163282
DNA
SEQ
-
-
2
David Baux
0000164148
00163283
DNA
SEQ
-
-
2
David Baux
0000164149
00163284
DNA
SEQ
-
-
2
Maria Bitner-Glindzicz
0000164150
00163285
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164151
00163286
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164152
00163287
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164153
00163288
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164154
00163289
DNA
SEQ
-
-
2
Maria Bitner-Glindzicz
0000164155
00163290
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164156
00163291
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164157
00163292
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164158
00163293
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164159
00163294
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164160
00163295
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164161
00163296
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164162
00163297
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164163
00163298
DNA
SEQ;SEQ-NG-S
-
-
1
Anne-Françoise Roux
0000164164
00163299
DNA
SEQ;SEQ-NG-S
-
-
1
Anne-Françoise Roux
0000164165
00163300
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164166
00163301
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164167
00163302
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164168
00163303
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164169
00163304
DNA
SEQ;SEQ-NG-S
-
-
1
Anne-Françoise Roux
0000164170
00163305
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164171
00163306
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164172
00163307
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164173
00163308
DNA
SEQ;SEQ-NG-S
-
-
1
Anne-Françoise Roux
0000164174
00163309
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164175
00163310
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164176
00163311
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164177
00163312
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164178
00163313
DNA
SEQ;SEQ-NG-S
-
-
1
Anne-Françoise Roux
0000164179
00163314
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164180
00163315
DNA
SEQ;SEQ-NG-S
-
-
2
Anne-Françoise Roux
0000164181
00163316
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164182
00163317
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164183
00163318
DNA
SEQ;SEQ-NG-S
-
-
4
Anne-Françoise Roux
0000164184
00163319
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164185
00163320
DNA
SEQ
-
-
5
David Baux
0000164186
00163321
DNA
SEQ
-
-
5
David Baux
0000164187
00163322
DNA
SEQ
-
-
5
David Baux
0000164188
00163323
DNA
SEQ
-
-
5
David Baux
0000164189
00163324
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164190
00163325
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164191
00163326
DNA
SEQ;SEQ-NG-S
-
-
1
Anne-Françoise Roux
0000164192
00163327
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164193
00163328
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164194
00163329
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164195
00163330
DNA
SEQ
-
-
2
Maria Bitner-Glindzicz
0000164196
00163331
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164197
00163332
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164198
00163333
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164199
00163334
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164200
00163335
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164201
00163336
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164202
00163337
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164203
00163338
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164204
00163339
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164205
00163340
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164206
00163341
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164207
00163342
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164208
00163343
DNA
SEQ;SEQ-NG-S
-
-
1
Anne-Françoise Roux
0000164209
00163344
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164210
00163345
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164211
00163346
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164212
00163347
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164213
00163348
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164214
00163349
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164215
00163350
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164216
00163351
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164217
00163352
DNA
SEQ
-
-
1
Maria Bitner-Glindzicz
0000164218
00163353
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164219
00163354
DNA
SEQ;SEQ-NG-S
-
-
1
Anne-Françoise Roux
0000164220
00163355
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164221
00163356
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164222
00163357
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164223
00163358
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164224
00163359
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164225
00163360
DNA
SEQ
-
-
1
David Baux
0000164226
00163361
DNA
SSCA
-
-
1
David Baux
0000164227
00163362
DNA
SSCA
-
-
1
David Baux
0000164228
00163363
DNA
SSCA
-
-
1
David Baux
0000164229
00163364
DNA
SSCA
-
-
1
David Baux
0000164230
00163365
DNA
SSCA
-
-
1
David Baux
0000164231
00163366
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164232
00163367
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164233
00163368
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164234
00163369
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164235
00163370
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164236
00163371
DNA
SEQ
-
-
1
Anne-Françoise Roux
0000164237
00163372
DNA
SEQ
-
-
1
Anne-Françoise Roux
10 per page
25 per page
50 per page
100 per page
Legend
How to query
« First
Prev
1
2
Next
Last »
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our
APIs
to retrieve data.
Powered by
LOVD v.3.0
Build 30b
LOVD software ©2004-2024
Leiden University Medical Center
Database contents © by their respective submitters and curators