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Phenotypic Abnormality (PA): Abnormal oral frenulum morphology

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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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + 5:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + 4:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + 3:   Abnormality of the mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + 2:   Abnormal oral morphology [HP:0031816] <6>(35|53) (44|30|21)
+ 1:   Abnormal oral cavity morphology [HP:0000163] <14>(28|43) (36|21|15)
0:   Abnormal oral frenulum morphology [HP:0000190] <3>(0|1) (0|1|1)
- 1:   Accessory oral frenulum [HP:0000191](0|0) (0|0|0)
- 1:   Ankyloglossia [HP:0010296](0|1) (0|1|1)
- 1:   Short lingual frenulum [HP:0000200](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.0003423Direct


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 (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.01675Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0005965Direct