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Phenotypic Abnormality (PA): Abnormality of the gingiva

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + + + + 8:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + 7:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + 6:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + 5:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + 4:   Abnormality of the mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + + 3:   Abnormal oral morphology [HP:0031816] <6>(35|53) (44|30|21)
+ + 2:   Abnormal oral cavity morphology [HP:0000163] <14>(28|43) (36|21|15)
+ 1:   Abnormal oral mucosa morphology [HP:0011830] <15>(10|16) (13|8|3)
0:   Abnormality of the gingiva [HP:0000168] <10>(3|7) (5|1|0)
- 1:   Periodontitis [HP:0000704] <3>(1|1) (1|0|0)
- 1:   Fusion of gums [HP:0012292](0|0) (0|0|0)
- 1:   Gingival bleeding [HP:0000225](1|1) (1|0|0)
- 1:   Gingival calcification [HP:0025141](0|0) (0|0|0)
- 1:   Gingival cleft [HP:0030690](0|0) (0|0|0)
- 1:   Gingival fibromatosis [HP:0000169](0|0) (0|0|0)
- 1:   Gingival hyperkeratosis [HP:0000222](0|0) (0|0|0)
- 1:   Gingival overgrowth [HP:0000212](0|0) (0|0|0)
- 1:   Gingival recession [HP:0030816](0|0) (0|0|0)
- 1:   Gingivitis [HP:0000230](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
Fibrinogen C-terminal domain-like0.000498Direct
Trypsin-like serine proteases0.002205Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
beta-glycanases0.0000412Direct
Fibrinogen C-terminal domain-like0.0002925Direct
Eukaryotic proteases0.0005956Direct
GLA-domain0.0009Direct
VWC domain0.0009Direct
PX domain0.0009Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
Fibrinogen C-terminal domain-like0.000252Direct
GLA-domain0.0008136Direct
PX domain0.0008136Direct
Trypsin-like serine proteases0.001248Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
64268,50044
  • 64268 - PX domain
  • 50044 - SH3-domain
  • 0Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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