Global Variome shared LOVD
TRPM1 (transient receptor potential cation channel,...)
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Curator:
Global Variome, with Curator vacancy
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All screenings for gene TRPM1
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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.
188 entries on 2 pages. Showing entries 1 - 100.
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How to query
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Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000033258
00033190
DNA
SEQ;SEQ-NG-S
-
-
2
Kornelia Neveling
0000033659
00033591
DNA
SEQ
-
-
2
Soumittra Nagasamy
0000033660
00033592
DNA
SEQ
-
-
1
Soumittra Nagasamy
0000033661
00033593
DNA
SEQ
-
-
2
Soumittra Nagasamy
0000033662
00033594
DNA
SEQ
-
-
2
Soumittra Nagasamy
0000033663
00033595
DNA
SEQ
-
-
2
Soumittra Nagasamy
0000033664
00033596
DNA
SEQ
-
-
1
Soumittra Nagasamy
0000156418
00155553
DNA
SEQ
-
-
1
Dror Sharon
0000156419
00155554
DNA
SEQ
-
-
1
Dror Sharon
0000156420
00155555
DNA
SEQ
-
-
1
Dror Sharon
0000156421
00155556
DNA
SEQ
-
-
1
Dror Sharon
0000309821
00308676
DNA
SEQ;SEQ-NG
-
204 gene panel
2
Global Variome, with Curator vacancy
0000310578
00309433
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310579
00309434
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310580
00309435
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310581
00309436
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000310582
00309437
DNA
SEQ
-
-
1
Global Variome, with Curator vacancy
0000329179
00327964
DNA
SEQ-NG
-
WES
2
LOVD
0000329251
00328036
DNA
SEQ-NG
-
WGS
1
LOVD
0000329259
00328044
DNA
SEQ-NG
-
WGS
1
LOVD
0000329384
00328169
DNA
SEQ-NG
-
WGS
2
LOVD
0000329487
00328272
DNA
SEQ-NG
-
WES and WGS
1
LOVD
0000329631
00328417
DNA
SEQ-NG
-
WES
1
LOVD
0000329695
00328480
DNA
SEQ-NG
-
gene panel
2
LOVD
0000329696
00328481
DNA
SEQ-NG
-
gene panel
1
LOVD
0000329697
00328482
DNA
SEQ-NG
-
gene panel
1
LOVD
0000329718
00328503
DNA
SEQ-NG
-
gene panel
2
LOVD
0000333761
00332537
DNA
SEQ-NG
-
gene panel
2
LOVD
0000334639
00333414
DNA
SEQ;SEQ-NG
-
184-gene panel
2
LOVD
0000334640
00333415
DNA
SEQ;SEQ-NG
-
184-gene panel
2
LOVD
0000335218
00333992
DNA
SEQ-NG
-
-
2
LOVD
0000335219
00333993
DNA
SEQ-NG
-
-
2
LOVD
0000364914
00363686
DNA
SEQ-NG
-
gene panel
1
LOVD
0000376585
00375388
DNA
SEQ
-
-
1
LOVD
0000376586
00375389
DNA
SEQ
-
-
1
LOVD
0000376587
00375390
DNA
SEQ
-
-
1
LOVD
0000376588
00375391
DNA
SEQ
-
-
1
LOVD
0000376589
00375392
DNA
SEQ
-
-
1
LOVD
0000376590
00375393
DNA
SEQ
-
-
1
LOVD
0000376591
00375394
DNA
SEQ
-
-
1
LOVD
0000376592
00375395
DNA
SEQ
-
-
1
LOVD
0000376593
00375396
DNA
SEQ
-
-
1
LOVD
0000376594
00375397
DNA
SEQ
-
-
1
LOVD
0000376595
00375398
DNA
SEQ
-
-
1
LOVD
0000376596
00375399
DNA
SEQ
-
-
1
LOVD
0000376597
00375400
DNA
SEQ
-
-
1
LOVD
0000376598
00375401
DNA
SEQ
-
-
1
LOVD
0000376599
00375402
DNA
SEQ
-
-
1
LOVD
0000376603
00375406
DNA
SEQ
-
-
1
LOVD
0000378051
00376846
DNA
SEQ
-
5-gene panel
1
LOVD
0000378052
00376847
DNA
SEQ
-
5-gene panel
1
LOVD
0000378054
00376849
DNA
SEQ
-
5-gene panel
1
LOVD
0000378055
00376850
DNA
SEQ
-
5-gene panel
1
LOVD
0000378056
00376851
DNA
SEQ
-
5-gene panel
2
LOVD
0000378057
00376852
DNA
SEQ
-
5-gene panel
1
LOVD
0000379145
00377941
DNA
SEQ; SEQ-NG-S
blood
-
1
LOVD
0000379162
00377958
DNA
SEQ; SEQ-NG-S
blood
-
1
LOVD
0000380629
00379429
DNA
SEQ
blood
WES
1
LOVD
0000380794
00379595
DNA
SEQ
blood
-
1
LOVD
0000380795
00379596
DNA
SEQ
blood
-
1
LOVD
0000380796
00379597
DNA
SEQ
blood
-
2
LOVD
0000380797
00379598
DNA
SEQ
blood
-
2
LOVD
0000380798
00379599
DNA
SEQ
blood
-
1
LOVD
0000380799
00379600
DNA
SEQ
blood
-
1
LOVD
0000381099
00379897
DNA
SEQ-NG
-
panel of 441 hereditary eye disease genes including 291 genes related to IRD
2
LOVD
0000382472
00381257
DNA
PCR;SEQ
blood
-
2
Martin Zenker, Prof. Dr. med.
0000382473
00381258
DNA
PCR;SEQ
blood
-
2
Martin Zenker, Prof. Dr. med.
0000382474
00381259
DNA
PCR;SEQ
blood
-
2
Martin Zenker, Prof. Dr. med.
0000382475
00381260
DNA
PCR;SEQ
blood
-
1
Martin Zenker, Prof. Dr. med.
0000382476
00381261
DNA
PCR;SEQ
blood
-
1
Martin Zenker, Prof. Dr. med.
0000382477
00381262
DNA
PCR;SEQ
blood
-
1
Martin Zenker, Prof. Dr. med.
0000382478
00381263
DNA
PCR;SEQ
blood
-
2
Martin Zenker, Prof. Dr. med.
0000382479
00381264
DNA
PCR;SEQ
blood
-
1
Martin Zenker, Prof. Dr. med.
0000382480
00381265
DNA
PCR;SEQ
blood
-
1
Martin Zenker, Prof. Dr. med.
0000383793
00382579
DNA
SEQ-NG-I
blood
125 genes associated with inherited retinal disorders, see paper supplemental data
2
LOVD
0000383820
00382606
DNA
SEQ-NG-I
blood
125 genes associated with inherited retinal disorders, see paper supplemental data
2
LOVD
0000384686
00383461
DNA
?
-
retrospective study
2
LOVD
0000384687
00383462
DNA
?
-
retrospective study
1
LOVD
0000384747
00383522
DNA
SEQ-NG-I
blood
204 genes associated with inherited retinal disorders; see paper
1
LOVD
0000385522
00384297
DNA
SEQ-NG
blood
panel of 126 genes
2
LOVD
0000386399
00385170
DNA
SEQ-NG-I
-
176 genes panel
2
LOVD
0000387918
00386690
DNA
SEQ-NG-I;PCRq
blood
-
2
LOVD
0000388055
00386827
DNA
SEQ-NG-I;SEQ
blood
-
2
LOVD
0000388867
00387641
DNA
SEQ-NG
blood
targeted sequencing
2
LOVD
0000388868
00387642
DNA
SEQ-NG
blood
targeted sequencing
1
LOVD
0000389711
00388470
DNA
SEQ-NG
-
CNV gene panel next-generation sequencing
2
LOVD
0000391647
00390406
DNA
SEQ-NG-I
blood
whole genome sequencing
1
LOVD
0000391648
00390407
DNA
SEQ-NG-I
blood
whole genome sequencing
1
LOVD
0000391649
00390408
DNA
SEQ-NG-I
blood
whole genome sequencing
2
LOVD
0000391650
00390409
DNA
SEQ-NG-I
blood
whole genome sequencing
1
LOVD
0000391985
00390744
DNA
SEQ-NG-I
blood
whole exome sequencing
1
LOVD
0000392830
00391588
DNA
?
blood
NGS gene panel investigation in 60 families, Sanger sequencing in 27 families, and Asper microarray in 25 families
2
LOVD
0000394879
00393631
DNA
SEQ-NG
-
hereditary eye disease enrichment panel (HEDEP)
2
LOVD
0000415480
00414201
DNA
SEQ
blood
-
1
LOVD
0000415481
00414202
DNA
SEQ
blood
-
1
LOVD
0000415482
00414203
DNA
SEQ
blood
-
1
LOVD
0000415483
00414204
DNA
SEQ
blood
-
2
LOVD
0000415484
00414205
DNA
SEQ
blood
-
2
LOVD
0000415485
00414206
DNA
SEQ
blood
-
2
LOVD
0000415487
00414207
DNA
SEQ
blood
-
1
LOVD
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