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Phenotypic Abnormality (PA): Abnormality of prenatal development or birth

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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)
+ 1:   Phenotypic abnormality [HP:0000118] <25>
0:   Abnormality of prenatal development or birth [HP:0001197] <18>(10|15) (12|5|3)
- 1:   Abnormal delivery [HP:0001787] <13>(6|5) (6|0|0)
- 1:   Fetal ultrasound soft marker [HP:0011425] <13>(0|2) (0|0|0)
- 1:   Prenatal maternal abnormality [HP:0002686] <13>(0|0) (1|0|0)
- 1:   Abnormalities of placenta or umbilical cord [HP:0001194] <4>(1|1) (1|1|1)
- 1:   Abnormality of the amniotic fluid [HP:0001560] <4>(0|2) (0|0|0)
- 1:   Hydrops fetalis [HP:0001789] <2>(0|0) (0|0|0)
- 1:   Low APGAR score [HP:0030917] <2>(0|0) (0|0|0)
- 1:   Premature birth [HP:0001622] <2>(0|0) (0|0|0)
- 1:   Prenatal movement abnormality [HP:0001557] <2>(4|4) (4|2|0)
- 1:   Increased nuchal translucency [HP:0010880] <1>(0|0) (0|0|0)
- 1:   Female fetal virilization [HP:0031170](0|0) (0|0|0)
- 1:   Fetal ascites [HP:0001791](0|0) (0|0|0)
- 1:   Fetal distress [HP:0025116](0|0) (0|0|0)
- 1:   Intrauterine fetal demise of one twin after midgestation [HP:0030753](0|0) (0|0|0)
- 1:   Lemon sign [HP:0032269](0|0) (0|0|0)
- 1:   Postterm pregnancy [HP:0031169](0|0) (0|0|0)
- 1:   Preimplantation lethality [HP:0032479](0|0) (0|0|0)
- 1:   Twin-to-twin transfusion [HP:0031110](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
Integrin domains0.00005472Direct
SNARE fusion complex0.01789Inherited
Fibrinogen C-terminal domain-like0.05069Inherited
Kelch motif0.05627Inherited
POZ domain0.07294Inherited
Tropomyosin0.08516Inherited
Nicotinic receptor ligand binding domain-like0.1327Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.1327Inherited
Complement control module/SCR domain0.482Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Fibrinogen coiled-coil and central regions0Direct
Integrin domains0.00003244Direct
Integrin alpha N-terminal domain0.0001578Direct
VWC domain0.0007744Direct
SNARE fusion complex0.01298Inherited
Extended AAA-ATPase domain0.02128Inherited
RecA protein-like (ATPase-domain)0.02629Inherited
Ras-binding domain, RBD0.02691Inherited
Fibrinogen C-terminal domain-like0.0402Inherited
Kelch motif0.04542Inherited
Tropomyosin0.07036Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.1141Inherited
Nicotinic receptor ligand binding domain-like0.1141Inherited
G proteins0.2934Inherited
Complement control module/SCR domain0.4547Inherited


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)
Fibrinogen coiled-coil and central regions0Direct
Integrin domains0.00002566Direct
Integrin alpha N-terminal domain0.0006875Direct
SNARE fusion complex0.01222Inherited
Fibrinogen C-terminal domain-like0.03776Inherited
Kelch motif0.04244Inherited
POZ domain0.05621Inherited
Tropomyosin0.06659Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.1076Inherited
Nicotinic receptor ligand binding domain-like0.1076Inherited
Cytochrome P4500.3802Inherited
Complement control module/SCR domain0.4392Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
69318,69179
  • 69318 - Integrin alpha N-terminal domain
  • 69179 - Integrin domains
  • 0.0001329Direct
    69179,69179
  • 69179 - Integrin domains
  • 69179 - Integrin domains
  • 0.0001329Direct
    53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.01222Inherited
    63712,90112
  • 63712 - Nicotinic receptor ligand binding domain-like
  • 90112 - Neurotransmitter-gated ion-channel transmembrane pore
  • 0.1076Inherited
    57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.331Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    69179,69179,69179
  • 69179 - Integrin domains
  • 69179 - Integrin domains
  • 69179 - Integrin domains
  • 0.0001329Direct
    69318,69179,69179
  • 69318 - Integrin alpha N-terminal domain
  • 69179 - Integrin domains
  • 69179 - Integrin domains
  • 0.0001329Direct
    57535,57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.06659Inherited


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