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Phenotypic Abnormality (PA): Abnormality of the sternum

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + 2:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ 1:   Abnormality of the thorax [HP:0000765] <12>(13|18) (14|8|7)
0:   Abnormality of the sternum [HP:0000766] <12>(1|2) (1|0|5)
- 1:   Abnormal sternal ossification [HP:0011863] <4>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the sternum [HP:0006714] <4>(0|0) (0|0|0)
- 1:   Abnormality of the xiphoid process [HP:0100892] <3>(0|0) (0|0|0)
- 1:   Pectus carinatum [HP:0000768] <1>(0|0) (0|0|0)
- 1:   Pectus excavatum [HP:0000767] <1>(1|1) (1|0|0)
- 1:   Bifid sternum [HP:0010309](0|0) (0|0|0)
- 1:   Bulging of the costochondral junction [HP:0000893](0|0) (0|0|0)
- 1:   Prominent sternum [HP:0000884](0|0) (0|0|0)
- 1:   Rachitic rosary [HP:0000897](0|0) (0|0|0)
- 1:   Sternal pit [HP:0410277](0|0) (0|0|0)
- 1:   Sternal punctate calcifications [HP:0006637](0|0) (0|0|0)
- 1:   Supraumbilical raphe [HP:0410276](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Calponin-homology domain, CH-domain0.004129Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Ras-binding domain, RBD0.0003553Direct
Calponin-homology domain, CH-domain0.002264Inherited


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)
Calponin-homology domain, CH-domain0.002464Inherited

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57581,57196
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 57196 - EGF/Laminin
  • 0Direct
    57196,57196,57581
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 0Direct
    57196,57581,57184
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 57184 - Growth factor receptor domain
  • 0Direct
    57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0Direct
    57184,57184,57196
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0.0006729Direct


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