Global Variome shared LOVD
TNNI2 (troponin I type 2 (skeletal, fast))
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
Curator:
Johan den Dunnen
View all genes
View TNNI2 gene homepage
View graphs about the TNNI2 gene database
Create a new gene entry
View all transcripts
View all transcripts of gene TNNI2
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene TNNI2
View all variants in gene TNNI2
Full data view for gene TNNI2
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 TNNI2
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene TNNI2
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene TNNI2
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
All screenings for gene TNNI2
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.
32 entries on 1 page. Showing entries 1 - 32.
10 per page
25 per page
50 per page
100 per page
Legend
How to query
Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000155360
00154502
DNA
SEQ-NG-I
Amniotic fluid, fetal cells
-
1
Andreas Laner
0000155364
00154506
DNA
SEQ
-
-
1
Johan den Dunnen
0000155365
00154507
DNA
SEQ
-
-
1
Johan den Dunnen
0000155366
00154508
DNA
SEQ
-
-
1
Johan den Dunnen
0000155367
00154509
DNA
SEQ
-
-
1
Johan den Dunnen
0000155368
00154510
DNA
SEQ
-
-
1
Johan den Dunnen
0000155369
00154511
DNA
HD;SEQ
-
-
1
Johan den Dunnen
0000155370
00154512
DNA
SEQ
-
-
1
Johan den Dunnen
0000155371
00154513
DNA
SEQ
-
-
1
Johan den Dunnen
0000155372
00154514
DNA
SEQ
-
-
1
Johan den Dunnen
0000155373
00154515
DNA
SEQ
-
-
1
Johan den Dunnen
0000155374
00154516
DNA
SEQ
-
-
1
Johan den Dunnen
0000155375
00154517
DNA
SEQ
-
-
1
Johan den Dunnen
0000155376
00154518
DNA
SEQ
-
-
1
Madhuri Hegde
0000155377
00154519
DNA
SEQ
-
-
1
Madhuri Hegde
0000155758
00154900
DNA
SEQ
-
-
1
Johan den Dunnen
0000155759
00154901
DNA
SEQ
-
-
1
Johan den Dunnen
0000155760
00154902
DNA
SEQ
-
-
1
Johan den Dunnen
0000155761
00154903
DNA
SEQ
-
-
1
Johan den Dunnen
0000155762
00154904
DNA
SEQ
-
-
1
Johan den Dunnen
0000155763
00154905
DNA
SEQ
-
-
1
Johan den Dunnen
0000155764
00154906
DNA
SEQ
-
-
1
Johan den Dunnen
0000155765
00154907
DNA
SEQ
-
-
1
Johan den Dunnen
0000155766
00154908
DNA
SEQ
-
-
1
Johan den Dunnen
0000155767
00154909
DNA
SEQ
-
-
1
Johan den Dunnen
0000308341
00307199
DNA
SEQ
-
-
1
Gianina Ravenscroft
0000308343
00307201
DNA
SEQ
-
-
1
Gianina Ravenscroft
0000308378
00307236
DNA
SEQ
-
-
1
Gianina Ravenscroft
0000308380
00307238
DNA
SEQ
-
-
1
Gianina Ravenscroft
0000308384
00307242
DNA
SEQ
-
-
1
Gianina Ravenscroft
0000308385
00307243
DNA
SEQ
-
-
1
Gianina Ravenscroft
0000308387
00307245
DNA
SEQ
-
-
1
Gianina Ravenscroft
10 per page
25 per page
50 per page
100 per page
Legend
How to query
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