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Phenotypic Abnormality (PA): Abnormal systemic arterial morphology

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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 cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + 2:   Abnormality of cardiovascular system morphology [HP:0030680] <3>(29|42) (31|19|20)
+ + 2:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ 1:   Abnormal vascular morphology [HP:0025015] <12>(15|18) (16|11|10)
0:   Abnormal systemic arterial morphology [HP:0011004] <24>(8|11) (9|4|2)
- 1:   Abnormal aortic morphology [HP:0001679] <16>(4|5) (4|2|2)
- 1:   Abnormal carotid artery morphology [HP:0005344] <12>(0|1) (0|0|0)
- 1:   Abnormal cerebral artery morphology [HP:0009145] <9>(3|3) (4|2|0)
- 1:   Abnormal coronary artery morphology [HP:0006704] <9>(0|1) (0|0|0)
- 1:   Abnormal retinal artery morphology [HP:0000630] <8>(1|0) (1|0|0)
- 1:   Arterial calcification [HP:0003207] <7>(0|0) (0|0|0)
- 1:   Arterial stenosis [HP:0100545] <6>(3|4) (4|2|0)
- 1:   Abnormal subclavian artery morphology [HP:0031251] <5>(0|0) (0|0|0)
- 1:   Arterial tortuosity [HP:0005116] <5>(0|0) (0|0|0)
- 1:   Abnormal renal artery morphology [HP:0008776] <3>(0|0) (0|0|0)
- 1:   Arteriosclerosis [HP:0002634] <3>(0|1) (0|0|0)
- 1:   Abnormal facial artery morphology [HP:3000024] <2>(0|0) (0|0|0)
- 1:   Abnormal vertebral artery morphology [HP:0030321] <2>(0|0) (0|0|0)
- 1:   Arteritis [HP:0012089] <2>(0|0) (0|0|0)
- 1:   Dilatation of an abdominal artery [HP:0002636] <2>(0|0) (0|0|0)
- 1:   Abnormal celiac artery morphology [HP:0012326] <1>(0|0) (0|0|0)
- 1:   Abnormal radial artery morphology [HP:0031640] <1>(0|0) (0|0|0)
- 1:   Arterial dissection [HP:0005294] <1>(1|1) (1|0|0)
- 1:   Cystic medial necrosis [HP:0012180] <1>(0|0) (0|0|0)
- 1:   Abnormal greater palatine artery morphology [HP:3000049](0|0) (0|0|0)
- 1:   Abnormal lacrimal artery morphology [HP:3000065](0|0) (0|0|0)
- 1:   Abnormal lingual artery morphology [HP:3000074](0|0) (0|0|0)
- 1:   Arterial fibromuscular dysplasia [HP:0005313](0|0) (0|0|0)
- 1:   Arterial intimal fibrosis [HP:0011353](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
SMAD MH1 domain0.004128Inherited
Myosin rod fragments0.01035Inherited
Tropomyosin0.02489Inherited
(Trans)glycosidases0.05183Inherited
Actin-like ATPase domain0.05532Inherited
Snake toxin-like0.111Inherited
SMAD/FHA domain0.1614Inherited
FnI-like domain0.3382Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Double-stranded RNA-binding domain (dsRBD)0.000802Direct
SMAD domain0.00289Inherited
SMAD MH1 domain0.00289Inherited
Actin/HSP700.004764Inherited
Myosin rod fragments0.007817Inherited
Erythroid transcription factor GATA-10.01218Inherited
Tropomyosin0.0196Inherited
VWC domain0.2166Inherited
RecA protein-like (ATPase-domain)0.2166Inherited
ABC transporter ATPase domain-like0.2437Inherited
Transforming growth factor (TGF)-beta0.2437Inherited


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)
SMAD MH1 domain0.002463Inherited
Myosin rod fragments0.006669Inherited
Tropomyosin0.01721Inherited
(Trans)glycosidases0.03834Inherited
Actin-like ATPase domain0.04116Inherited
MHC antigen-recognition domain0.04608Inherited
Snake toxin-like0.08762Inherited
SMAD/FHA domain0.1323Inherited
FnI-like domain0.2968Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57184,57196
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0.01443Inherited
    53067,53067
  • 53067 - Actin-like ATPase domain
  • 53067 - Actin-like ATPase domain
  • 0.0259Inherited
    54452,48726
  • 54452 - MHC antigen-recognition domain
  • 48726 - Immunoglobulin
  • 0.04608Inherited
    57196,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.3655Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57184,57196
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0.001014Inherited
    57196,57184,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 0.1323Inherited


    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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