Global Variome shared LOVD
GATA1 (GATA binding protein 1 (globin transcriptio...))
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Phenotypes for disease #00389 (TOF (tetralogy of Fallot (TOF)), OMIM:187500)
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
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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'
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94 entries on 1 page. Showing entries 1 - 94.
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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
0000027867
Tetralogy of Fallot
-
-
Isolated (sporadic)
-
-
-
-
-
Marta Sanchez Castro
00034470
0000027868
Tetralogy of Fallot
-
-
Isolated (sporadic)
-
-
-
-
-
Marta Sanchez Castro
00034471
0000027869
Tetralogy of Fallot
-
-
Isolated (sporadic)
-
-
-
-
-
Marta Sanchez Castro
00034473
0000027871
Tetralogy of Fallot
-
-
Isolated (sporadic)
-
-
-
-
-
Marta Sanchez Castro
00034474
0000027872
Tetralogy of Fallot
-
-
Isolated (sporadic)
-
-
-
-
-
Marta Sanchez Castro
00034475
0000027874
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034476
0000027875
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034477
0000027876
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034478
0000027877
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034479
0000027878
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034480
0000027879
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034481
0000027880
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034482
0000027881
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034483
0000027882
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034484
0000027883
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034485
0000027884
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034486
0000027885
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034487
0000027886
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034488
0000027887
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034489
0000027888
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034490
0000027889
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034491
0000027890
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034492
0000027891
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034493
0000027892
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034494
0000027893
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034495
0000027894
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034496
0000027895
Tetralogy of Fallot
-
-
Familial
-
-
-
-
-
Marta Sanchez Castro
00034497
0000167988
atrioventricular septal defect, patent ductus arteriosus, atrial fibrillation
tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Yi-Qing Yang
00222788
0000167989
atrial septal defect
tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Yi-Qing Yang
00222789
0000167990
-
tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Yi-Qing Yang
00222790
0000179811
see paper; …
Tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00239597
0000179812
see paper; …
Tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00239598
0000179813
see paper; …
Tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00239599
0000179814
see paper; …
Tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00239600
0000179815
see paper; …
Tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00239601
0000179816
see paper; …
Tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00239602
0000179817
see paper; …
Tetralogy of Fallot
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00239603
0000179818
see paper; …
Tetralogy of Fallot
-
Unknown
-
-
-
-
-
Johan den Dunnen
00239604
0000179819
see paper; …
Tetralogy of Fallot
-
Unknown
-
-
-
-
-
Johan den Dunnen
00239605
0000179832
see paper; ...
Tetralogy of Fallot
-
Unknown
-
-
-
-
-
Johan den Dunnen
00239618
0000179833
see paper; ...
Tetralogy of Fallot
-
Unknown
-
-
-
-
-
Johan den Dunnen
00239619
0000179834
Alagille facies, mild mental retardation, RAA, singular origin of left subclavian artery, truncus bicaroticus
Tetralogy of Fallot
-
Unknown
-
-
-
-
-
Johan den Dunnen
00239620
0000179835
Alagille facies, severe mental retardation, hypernasality, dysplastic ears, flat nasal bridge, wide-set nipples, extrahepatic biliary atresia, peripheral pulmonary stenosis
Tetralogy of Fallot
-
Unknown
-
-
-
-
-
Johan den Dunnen
00239621
0000204384
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266674
0000204393
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266678
0000204400
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266679
0000204407
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266682
0000204414
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266685
0000204426
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266691
0000204434
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266693
0000204439
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266696
0000204456
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266714
0000204464
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266718
0000204478
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266721
0000204504
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266734
0000204512
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266737
0000204519
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266738
0000204522
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266739
0000204529
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266741
0000204531
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266742
0000204533
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266743
0000204539
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266744
0000204542
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266745
0000204549
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266752
0000204592
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266776
0000204600
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266778
0000204618
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266786
0000204625
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266788
0000204627
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266792
0000204629
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266795
0000204649
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266819
0000204652
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266823
0000204654
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266824
0000204662
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266827
0000204664
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266828
0000204666
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266829
0000204685
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266839
0000204688
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266844
0000204694
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266845
0000204701
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266850
0000204703
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266851
0000204709
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266852
0000204734
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266873
0000204771
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266902
0000204798
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266921
0000204835
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266941
0000204853
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266953
0000204875
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266963
0000204886
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266972
0000204888
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266973
0000204900
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266975
0000204905
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266979
0000204923
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266999
0000335931
see paper; ..., tetralogy of Fallot, congenital heart disease
tetralogy of Fallot
ASD4
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00446729
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