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Phenotypic Abnormality (PA): Abnormality of the female genitalia

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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 genitourinary system [HP:0000119] <5>(73|72) (80|28|9)
+ + 2:   Abnormality of the genital system [HP:0000078] <3>(35|34) (37|10|3)
+ 1:   Abnormal reproductive system morphology [HP:0012243] <10>(28|27) (29|4|1)
0:   Abnormality of the female genitalia [HP:0010460] <2>(16|18) (18|2|0)
- 1:   Abnormality of female external genitalia [HP:0000055] <7>(3|2) (3|0|0)
- 1:   Abnormality of female internal genitalia [HP:0000008] <5>(14|16) (16|2|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
Fibrinogen coiled-coil and central regions0Direct
DNA repair protein MutS, domain III0Direct
Nuclear receptor ligand-binding domain0.004366Inherited
NagB/RpiA/CoA transferase-like0.007348Inherited
GroEL equatorial domain-like0.01261Inherited
RING/U-box0.02124Inherited
ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase0.06031Inherited
BRCT domain0.06031Inherited
Ribosomal protein S5 domain 2-like0.0902Inherited
Fibrinogen C-terminal domain-like0.09767Inherited
CalX-like0.1574Inherited
WD40 repeat-like0.1586Inherited
"Winged helix" DNA-binding domain0.2454Inherited
Trypsin-like serine proteases0.2755Inherited
Cytochrome P4500.3883Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
DIX domain0Direct
IF2B-like0Direct
DNA repair protein MutS, domain III0Direct
Fibrinogen coiled-coil and central regions0Direct
Smc hinge domain0Direct
DNA gyrase/MutL, N-terminal domain0.0004523Direct
DNA gyrase/MutL, second domain0.0004523Direct
Nuclear receptor ligand-binding domain0.002572Inherited
Nuclear receptor0.004713Inherited
Extended AAA-ATPase domain0.01508Inherited
Extracellular domain of cell surface receptors0.01839Inherited
Fibrinogen C-terminal domain-like0.07694Inherited
RecA protein-like (ATPase-domain)0.1239Inherited
CalX-beta domain0.1285Inherited
Eukaryotic proteases0.1558Inherited
Ngr ectodomain-like0.1593Inherited
ABC transporter ATPase domain-like0.2528Inherited
Rhodopsin-like0.293Inherited


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
Smc hinge domain0Direct
DNA repair protein MutS, domain III0Direct
Nuclear receptor ligand-binding domain0.002628Inherited
NagB/RpiA/CoA transferase-like0.004624Inherited
GroEL equatorial domain-like0.008269Inherited
RING/U-box0.01453Inherited
ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase0.04532Inherited
BRCT domain0.04532Inherited
Glucocorticoid receptor-like (DNA-binding domain)0.05784Inherited
Ribosomal protein S5 domain 2-like0.07023Inherited
Fibrinogen C-terminal domain-like0.07653Inherited
CalX-like0.1289Inherited
WD40 repeat-like0.1299Inherited
"Winged helix" DNA-binding domain0.209Inherited
Trypsin-like serine proteases0.2374Inherited
Cytochrome P4500.3452Inherited
Family A G protein-coupled receptor-like0.3811Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
48334,52540
  • 48334 - DNA repair protein MutS, domain III
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 0Direct
    55874,54211
  • 55874 - ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
  • 54211 - Ribosomal protein S5 domain 2-like
  • 0.0004172Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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