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Phenotypic Abnormality (PA): Hyperlipidemia

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(75|82) (79|40|16)
+ + 2:   Abnormal circulating metabolite concentration [HP:0032180] <12>(30|31) (31|14|4)
+ 1:   Abnormal circulating lipid concentration [HP:0003119] <6>(6|5) (6|2|1)
0:   Hyperlipidemia [HP:0003077] <2>(2|1) (2|0|1)
- 1:   Hypertriglyceridemia [HP:0002155] <1>(2|1) (2|0|0)
- 1:   Transient hyperlipidemia [HP:0008279](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)
N-terminal nucleophile aminohydrolases (Ntn hydrolases)0.0002713Direct
alpha/beta-Hydrolases0.227Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Proteasome subunits0Direct


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)
N-terminal nucleophile aminohydrolases (Ntn hydrolases)0.0001324Direct
alpha/beta-Hydrolases0.1921Inherited

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57535,57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.0006364Direct


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