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Phenotypic Abnormality (PA): Abnormality of the dentition

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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:   Abnormality of the dentition [HP:0000164] <18>(5|11) (8|5|3)
- 1:   Misalignment of teeth [HP:0000692] <9>(1|1) (1|1|1)
- 1:   Abnormality of dental morphology [HP:0006482] <8>(0|1) (0|1|0)
- 1:   Abnormality of dental structure [HP:0011061] <8>(2|5) (2|2|0)
- 1:   Abnormality of primary teeth [HP:0006481] <7>(0|0) (0|0|0)
- 1:   Abnormal number of teeth [HP:0006483] <4>(1|2) (3|0|0)
- 1:   Abnormality of dental eruption [HP:0006292] <4>(1|2) (2|0|0)
- 1:   Abnormality of the incisor [HP:0000676] <3>(0|0) (0|0|0)
- 1:   Odontogenic neoplasm [HP:0100612] <3>(0|0) (0|0|0)
- 1:   Periodontitis [HP:0000704] <3>(1|1) (1|0|0)
- 1:   Abnormality of molar [HP:0011077] <2>(0|0) (0|0|0)
- 1:   Abnormality of premolar [HP:0011076] <2>(0|0) (0|0|0)
- 1:   Premature loss of teeth [HP:0006480] <2>(1|1) (1|0|0)
- 1:   Abnormality of canine [HP:0011078] <1>(0|0) (0|0|0)
- 1:   Abnormality of the periodontium [HP:0410026] <1>(0|0) (0|0|0)
- 1:   Buried teeth encased in mucopolysaccharide [HP:0006326](0|0) (0|0|0)
- 1:   Fragile teeth [HP:0025124](0|0) (0|0|0)
- 1:   Irregular dentition [HP:0040079](0|0) (0|0|0)
- 1:   Periapical bone loss [HP:0000700](0|0) (0|0|0)


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

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
Helical domain of Sec23/240.1401Inherited
C-terminal, gelsolin-like domain of Sec23/240.1401Inherited
Ubiquitin-like0.372Inherited
Trypsin-like serine proteases0.5694Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
DIX domain0.007747Inherited
VWC domain0.0714Inherited
Fibroblast growth factors (FGF)0.0734Inherited
Helical domain of Sec23/240.1213Inherited
Trunk domain of Sec23/240.1213Inherited
beta-sandwich domain of Sec23/240.1213Inherited
C-terminal, gelsolin-like domain of Sec23/240.1213Inherited
PX domain0.1764Inherited
Laminin-type module0.3207Inherited
Eukaryotic proteases0.569Inherited


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)
Smc hinge domain0Direct
DPP6 N-terminal domain-like0.02142Inherited
Helical domain of Sec23/240.1137Inherited
C-terminal, gelsolin-like domain of Sec23/240.1137Inherited
PX domain0.1641Inherited
Cytokine0.3128Inherited
Ubiquitin-like0.3293Inherited
Trypsin-like serine proteases0.5263Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
141072,141072
  • 141072 - CalX-like
  • 141072 - CalX-like
  • 0Direct
    55486,82895
  • 55486 - Metalloproteases ("zincins"), catalytic domain
  • 82895 - TSP-1 type 1 repeat
  • 0.04299Inherited
    81811,82754
  • 81811 - Helical domain of Sec23/24
  • 82754 - C-terminal, gelsolin-like domain of Sec23/24
  • 0.1137Inherited
    57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.1683Inherited
    50978,50978
  • 50978 - WD40 repeat-like
  • 50978 - WD40 repeat-like
  • 0.3989Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    63825,57196,63825
  • 63825 - YWTD domain
  • 57196 - EGF/Laminin
  • 63825 - YWTD domain
  • 0Direct
    141072,141072,141072
  • 141072 - CalX-like
  • 141072 - CalX-like
  • 141072 - CalX-like
  • 0Direct
    57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.1137Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
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