Global Variome shared LOVD
ANKRD20A11P (ankyrin repeat domain 20 family member...)
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Phenotypes for disease #00202 (SGS (Shprintzen-Goldberg craniosynostosis syndrome (SGS)), OMIM:182212)
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
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Date
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39 entries on 1 page. Showing entries 1 - 39.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000039756
craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; no C1/2 spine malformation; hypotonia; developmental delay; mitral valve prolapse; aortic root dilatation; dural ectasia; no ectopia lentis; no cleft palate; no cleft palate; no club foot deformity; no arterial tortuosity; splenic artery aneurysm
-
-
Isolated (sporadic)
43y
-
-
-
-
Johan den Dunnen
00053031
0000039757
craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; noproptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; no C1/2 spine malformation; hypotonia; developmental delay; mitral valve prolapse; aortic root dilatation; dural ectasia; no ectopia lentis; no cleft palate; broad/bifid uvula; no club foot deformity; no arterial tortuosity; no other aneurysm
-
-
Isolated (sporadic)
6y
-
-
-
-
Johan den Dunnen
00053032
0000039758
craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; hypotonia; developmental delay; mitral valve prolapse; aortic root dilatation; no ectopia lentis; no cleft palate; club foot deformity
-
-
Isolated (sporadic)
16y
-
-
-
-
Johan den Dunnen
00053033
0000039759
craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; C1/2 spine malformation; hypotonia; developmental delay; no mitral valve prolapse; aortic root dilatation; no ectopia lentis; cleft palate; no cleft palate; no club foot deformity; no arterial tortuosity; no other aneurysm
-
-
Isolated (sporadic)
12y
-
-
-
-
Johan den Dunnen
00053034
0000039760
craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; C1/2 spine malformation; hypotonia; developmental delay; no mitral valve prolapse; aortic root dilatation; no ectopia lentis; no cleft palate; no club foot deformity
-
-
Isolated (sporadic)
22y
-
-
-
-
Johan den Dunnen
00053035
0000039761
craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; noproptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; hypotonia; developmental delay; aortic root dilatation; no ectopia lentis; no cleft palate
-
-
Isolated (sporadic)
21y
-
-
-
-
Johan den Dunnen
00053036
0000039762
craniosynostosis; no dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; no camptodactyly; scoliosis; pectus deformity; joint hypermobility; no joint contracture; hypotonia; developmental delay; aortic root dilatation; no ectopia lentis; cleft palate; no club foot deformity
-
-
Isolated (sporadic)
2y
-
-
-
-
Johan den Dunnen
00053037
0000039763
craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; no camptodactyly; no scoliosis; no pectus deformity; joint hypermobility; joint contracture; hypotonia; developmental delay; no mitral valve prolapse; no aortic root dilatation; no ectopia lentis; cleft palate; club foot deformity; splenic artery aneurysm with spontaneous rupture (blank cells, not determined)
-
-
Isolated (sporadic)
6y
-
-
-
-
Johan den Dunnen
00053038
0000039764
craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; no scoliosis; pectus deformity; joint hypermobility; joint contracture; C1/2 spine malformation; hypotonia; developmental delay; mitral valve prolapse; no aortic root dilatation; no ectopia lentis; no cleft palate; no broad/bifid uvula; no club foot deformity
-
-
Isolated (sporadic)
5y
-
-
-
-
Johan den Dunnen
00053039
0000039765
craniosynostosis; dolichocephaly; hypertelorism; down-slanting eyes; proptosis; malar hypoplasia; high/narrow palate; micrognathia; low set ears; arachnodactyly; camptodactyly; scoliosis; pectus deformity; joint hypermobility; joint contracture; C1/2 spine malformation; hypotonia; developmental delay; mitral valve prolapse; aortic root dilatation; dural ectasia; no ectopia lentis; no cleft palate; broad/bifid uvula; no club foot deformity; arterial tortuosity; no other aneurysm
-
-
Isolated (sporadic)
4y
-
-
-
-
Johan den Dunnen
00053040
0000039766
craniosynostosis, no arachnodactyly, pectus deformity, no scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia
-
-
Isolated (sporadic)
21y
-
-
-
-
Johan den Dunnen
00053041
0000039768
no craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia
-
-
Familial, autosomal dominant
42y
-
-
-
-
Johan den Dunnen
00053043
0000039769
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia
-
-
Familial, autosomal dominant
22y
-
-
-
-
Johan den Dunnen
00053044
0000039770
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia
-
-
Isolated (sporadic)
20y
-
-
-
-
Johan den Dunnen
00053045
0000039771
no craniosynostosis, arachnodactyly, no pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, no proptosis, downslanting palpebral fissures, no micrognathia/retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia
-
-
Familial, autosomal dominant
11y
-
-
-
-
Johan den Dunnen
00053046
0000039772
no craniosynostosis, arachnodactyly, no pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia; 44y-died of respiratory insufficiency
-
-
Familial, autosomal dominant
44y
-
-
-
-
Johan den Dunnen
00053047
0000039773
no craniosynostosis, arachnodactyly, no pectus deformity, no scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, no micrognathia/retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia
-
-
Familial, autosomal dominant
13y
-
-
-
-
Johan den Dunnen
00053048
0000039774
no craniosynostosis, arachnodactyly, no pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, no proptosis, downslanting palpebral fissures, no micrognathia/retrognathia, intellectual disability, no hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia
-
-
Familial, autosomal dominant
14y
-
-
-
-
Johan den Dunnen
00053049
0000039775
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia
-
-
Familial, autosomal dominant
22y
-
-
-
-
Johan den Dunnen
00053050
0000039776
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, no proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, myopia?
-
-
Familial, autosomal dominant
20y
-
-
-
-
Johan den Dunnen
00053051
0000039777
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, no joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, mitral valve prolapse, aortic dilatation requiring surgery (16y, aortic root dilatation with Z score=7.014), vertebrobasilar and internal carotid tortuosity, dilated pulmonary-artery root, no myopia
-
-
Isolated (sporadic)
18y
-
-
-
-
Johan den Dunnen
00053052
0000039778
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, no proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, no hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia
-
-
Isolated (sporadic)
16y
-
-
-
-
Johan den Dunnen
00053053
0000039779
no craniosynostosis, arachnodactyly, pectus deformity, no scoliosis, no joint contractures, no camptodactyly, no foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia
-
-
Isolated (sporadic)
5y
-
-
-
-
Johan den Dunnen
00053054
0000039780
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, mitral valve prolapse, no aortic root dilatation, no myopia
-
-
Isolated (sporadic)
21y
-
-
-
-
Johan den Dunnen
00053055
0000039781
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, no downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, mitral valve prolapse, mitral insufficiency, aortic root dilatation upper normal limit, myopia; 10y died suddenly, autopsy showed severe mitral valve dysplasia with calcifications mitral annulus
-
-
Isolated (sporadic)
10y
-
-
-
-
Johan den Dunnen
00053056
0000039782
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, no scaphocephaly/dolichocephaly, no hypertelorism, proptosis, downslanting palpebral fissures, no micrognathia/retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, mitral valve prolapse, aortic root dilatation, no myopia
-
-
Isolated (sporadic)
11y
-
-
-
-
Johan den Dunnen
00053057
0000039783
no craniosynostosis, arachnodactyly, pectus deformity, scoliosis, no joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, mitral valve prolapse, mitral insufficiency, aortic root dilatation, myopia
-
-
Isolated (sporadic)
32y
-
-
-
-
Johan den Dunnen
00053058
0000039784
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, joint contractures, camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, no downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia
-
-
Isolated (sporadic)
20y
-
-
-
-
Johan den Dunnen
00053059
0000039785
craniosynostosis, arachnodactyly, pectus deformity, scoliosis, no joint contractures, camptodactyly, no foot malposition, scaphocephaly or dolichocephaly, hypertelorism, proptosis, no downslanting palpebral fissures, micrognathia or retrognathia, intellectual disability, hernias, no loss of subcutaneous fat, no valvular anomalies, no aortic root dilatation, no myopia
-
-
Familial, autosomal dominant
26y
-
-
-
-
Johan den Dunnen
00053060
0000230406
Scoliosis (HP:0002650), Bifid uvula (HP:0000193), Wide anterior fontanel (HP:0000260)
Shprintzen-Goldberg syndrome
SGS
Isolated (sporadic)
3m
-
-
-
-
Katta M Girisha
00303329
0000299892
Proptosis, Generalized hypotonia, Dystonia, Plagiocephaly, Failure to thrive, Scoliosis
-
-
Unknown
00y06m
-
-
-
-
Andreas Laner
00407762
0000309911
see paper (extensive phenotyping)
Shprintzen-Goldberg craniosynostosis syndrome
SGS
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00418574
0000309912
see paper (extensive phenotyping)
Shprintzen-Goldberg craniosynostosis syndrome
SGS
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00418575
0000309913
see paper (extensive phenotyping)
Shprintzen-Goldberg craniosynostosis syndrome
SGS
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00418576
0000309914
see paper (extensive phenotyping)
Shprintzen-Goldberg craniosynostosis syndrome
SGS
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00418577
0000310070
hypermetropy, joint hypermobility, mitral valve prolapse, polyvalvular dysplasia/ insufficiency, kyphoscoliosis , bilateral inguinal hernias
Aortic valvular disease
Shprintzen–Goldberg Syndrome
Unknown
-
-
-
-
-
Carmela Fusco
00418774
0000310071
mitral valve prolapse, aneurismatic ovale fossa, megalocornea, joint hypermobility, Intellectual disability
Aortic valvular disease
Shprintzen–Goldberg Syndrome
Familial
-
-
-
-
-
Carmela Fusco
00418775
0000343212
Hypotonia, Mild global developmental delay, Pectus excavatum, Scapular winging, Atrial septal defect, Mildly elevated creatine kinase, Oligohydramnios
-
-
Isolated (sporadic)
08y
-
-
-
-
Andreas Laner
00454565
0000350492
Intellectual disability, Delayed speech and language development, Obesity, Brachycephaly, Anteverted nares, Synophrys, Abnormal dental enamel morphology, Short stature, Microcephaly, Neurodevelopmental delay
-
-
Unknown
13y
-
-
-
-
Andreas Laner
00464463
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