NDDVD - Neurodegenerative Diseases Variation Database
CHCHD10 (coiled-coil-helix-coiled-coil-helix domain...)
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Curator:
Y Yang
View all genes
View CHCHD10 gene homepage
View graphs about the CHCHD10 gene database
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View all transcripts
View all transcripts of gene CHCHD10
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View all variants
View all variants affecting transcripts
View unique variants in gene CHCHD10
View all variants in gene CHCHD10
Full data view for gene CHCHD10
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View all individuals
View all individuals with variants in gene CHCHD10
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View all diseases
View all diseases associated with gene CHCHD10
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View available phenotype columns
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View all screenings for gene CHCHD10
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All individuals with variants in gene CHCHD10
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.
Reference
: Reference to publication describing the individual/family, possibly giving more phenotypic details than listed in this database entry, including link to PubMed or other source, e.g. "den Dunnen ASHG2003 P2346". References in the "Country:City" format indicate that the variant was submitted directly to this database by the laboratory indicated.
Ethnic origin
: The ethnic origin of the individual; e.g. African, Caucasian, gypsy, jew (Ashkenazi).
Remarks
: Remarks about the individual.
Variants in genes
: The individual has variants for this gene.
Panel size
: Number of individuals this entry represents; e.g. 1 for an individual, 5 for a family with 5 affected members.
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.
24 entries on 1 page. Showing entries 1 - 24.
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Legend
How to query
Individual ID
Reference
Ethnic origin
Remarks
Disease
Phenotype details
Variants
Panel size
Owner
00000799
Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore DG, et al. (2014)
-
-
ALS, FTLD
-
1
1
Y Yang
00005190
ChiĆ² A et al. (2015)
-
-
ALS, FTLD
-
1
1
XY Liu
00005294
Teyssou E et al. (2016)
French
-
ALS
-
1
1
XY Liu
00005295
Teyssou E et al. (2016)
French
-
ALS
-
1
1
XY Liu
00005296
Teyssou E et al. (2016)
French
-
ALS
-
1
1
XY Liu
00005297
Teyssou E et al. (2016)
French
-
ALS
-
1
1
XY Liu
00005328
Xiao T et al. (2016)
-
-
AD
-
1
1
XY Liu
00005405
Shen S et al. (2017)
Chinese
-
ALS
-
1
1
XY Liu
00005406
Shen S et al. (2017)
Chinese
-
ALS
-
1
1
XY Liu
00005407
Shen S et al. (2017)
Chinese
-
ALS
-
1
1
XY Liu
00006078
Abdelkarim S et al. (2016)
-
not a highly penetrant pathogenic variant
FTLD
-
1
1
XY Liu
00006081
Jiao B et al. (2016)
-
-
FTLD
-
1
1
XY Liu
00006082
Jiao B et al. (2016)
-
-
FTLD
-
1
1
XY Liu
00006083
Jiao B et al. (2016)
-
-
FTLD
-
1
1
XY Liu
00006084
Jiao B et al. (2016)
-
-
FTLD
-
1
1
XY Liu
00006085
Jiao B et al. (2016)
-
-
FTLD
-
1
1
XY Liu
00006476
QingQing Zhou, et al. (2017)
Chinese
-
ALS
-
1
1
XY Liu
00006477
QingQing Zhou, et al. (2017)
Chinese
-
ALS
-
1
1
XY Liu
00006478
QingQing Zhou, et al. (2017)
Chinese
-
ALS
-
1
1
XY Liu
00006482
Shen Shen, et al. (2017)
Chinese
-
ALS
-
1
1
XY Liu
00006526
Carina Lehmer, et al. (2018)
-
-
ALS
-
1
1
XY Liu
00006527
Carina Lehmer, et al. (2018)
-
-
ALS
-
1
1
XY Liu
00006528
Carina Lehmer, et al. (2018)
-
-
ALS
-
1
1
XY Liu
00006529
Carina Lehmer, et al. (2018)
-
-
ALS
-
1
1
XY Liu
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Legend
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