Global Variome shared LOVD
ZBTB14 (zinc finger and BTB domain containing 14)
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
Curator:
Global Variome, with Curator vacancy
View all genes
View ZBTB14 gene homepage
View graphs about the ZBTB14 gene database
Create a new gene entry
View all transcripts
View all transcripts of gene ZBTB14
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene ZBTB14
View all variants in gene ZBTB14
Full data view for gene ZBTB14
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 ZBTB14
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene ZBTB14
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene ZBTB14
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
Phenotypes for disease #00254 (RTD (dysgenesis, renal tubular (RTD)), OMIM:267430)
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.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
Protein
: result from protein staining
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.
50 entries on 1 page. Showing entries 1 - 50.
10 per page
25 per page
50 per page
100 per page
Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000002785
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003990
0000002786
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003991
0000002787
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003992
0000002788
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003993
0000002789
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003994
0000002790
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003995
0000002791
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003996
0000002792
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003997
0000002793
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003998
0000002794
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00003999
0000002795
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004000
0000002796
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004001
0000002797
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004002
0000002798
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004003
0000002799
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004004
0000002800
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004005
0000002801
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004006
0000002802
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004007
0000002803
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004008
0000002804
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004009
0000002805
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004010
0000002806
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004012
0000002808
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004013
0000002809
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004014
0000002810
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004015
0000002812
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004017
0000002813
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004018
0000002814
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004019
0000002815
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004020
0000002816
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Olivier Gribouval
00004021
0000002817
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Olivier Gribouval
00004022
0000002818
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004023
0000002819
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004024
0000002820
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004025
0000002821
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004026
0000002822
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004027
0000002823
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004028
0000002824
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004029
0000002825
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004030
0000002826
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004031
0000002827
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004032
0000002828
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004033
0000002829
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004034
0000002830
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004035
0000002831
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004036
0000002832
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004037
0000002835
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004040
0000002836
-
-
-
Unknown
-
-
-
-
-
Olivier Gribouval
00004041
0000060371
Renal tubular dysgenesis (OMIM:267430)
-
-
Familial, autosomal recessive
-
-
-
-
-
Daniel Trujillano
00080802
0000342156
Renal insufficiency, Anhydramnios, Abnormality of prenatal development or birth; 3 missed abortions
-
-
Familial, autosomal recessive
28+0
-
-
-
-
Andreas Laner
00453498
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