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Phenotypic Abnormality (PA): Involuntary movements

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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 the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + 2:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ 1:   Abnormality of movement [HP:0100022] <19>(23|25) (25|14|3)
0:   Involuntary movements [HP:0004305] <13>(6|4) (6|4|0)
- 1:   Myoclonus [HP:0001336] <11>(1|3) (3|2|0)
- 1:   Stereotypy [HP:0000733] <7>(3|2) (3|1|0)
- 1:   Tremor [HP:0001337] <4>(0|0) (0|1|0)
- 1:   Clonus [HP:0002169] <3>(0|0) (0|0|0)
- 1:   Fasciculations [HP:0002380] <3>(0|0) (0|1|0)
- 1:   Tics [HP:0100033] <2>(0|0) (0|0|0)
- 1:   Chorea [HP:0002072] <1>(0|0) (0|0|0)
- 1:   Alien limb phenomenon [HP:0032506](0|0) (0|0|0)
- 1:   Athetosis [HP:0002305](0|0) (0|0|0)
- 1:   Chvostek sign [HP:0031990](0|0) (0|0|0)
- 1:   Hemiballismus [HP:0100248](0|0) (0|0|0)
- 1:   Paroxysmal dyskinesia [HP:0007166](0|0) (0|0|0)
- 1:   Self-mutilation of tongue and lips due to involuntary movements [HP:0008767](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
HIT-like0Direct
Cytochrome b5-like heme/steroid binding domain0Direct
Voltage-gated potassium channels0.0002443Direct
Acyl-CoA N-acyltransferases (Nat)0.1603Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.4341Inherited
Nicotinic receptor ligand binding domain-like0.4341Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Cytochrome b50Direct
Tetramerization domain of potassium channels0.009411Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.3975Inherited
Nicotinic receptor ligand binding domain-like0.3975Inherited


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)
Cytochrome b5-like heme/steroid binding domain0Direct
HIT-like0Direct
Voltage-gated potassium channels0.0001187Direct
Acyl-CoA N-acyltransferases (Nat)0.1313Inherited
Nicotinic receptor ligand binding domain-like0.3902Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.3902Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53822,53850
  • 53822 - Periplasmic binding protein-like I
  • 53850 - Periplasmic binding protein-like II
  • 0Direct
    48371,48371
  • 48371 - ARM repeat
  • 48371 - ARM repeat
  • 0.1283Inherited
    63712,90112
  • 63712 - Nicotinic receptor ligand binding domain-like
  • 90112 - Neurotransmitter-gated ion-channel transmembrane pore
  • 0.3902Inherited
    54928,54928
  • 54928 - RNA-binding domain, RBD
  • 54928 - RNA-binding domain, RBD
  • 0.5812Inherited


    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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