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Phenotypic Abnormality (PA): Abnormal testis 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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the genitourinary system [HP:0000119] <5>(73|72) (80|28|9)
+ + + + 4:   Abnormality of the genital system [HP:0000078] <3>(35|34) (37|10|3)
+ + + 3:   Abnormal reproductive system morphology [HP:0012243] <10>(28|27) (29|4|1)
+ + 2:   Abnormal external genitalia [HP:0000811] <7>(15|11) (16|1|1)
+ + 2:   Abnormality of the male genitalia [HP:0010461] <2>(14|11) (16|1|1)
+ 1:   Abnormality of male external genitalia [HP:0000032] <9>(13|10) (15|1|1)
0:   Abnormal testis morphology [HP:0000035] <21>(9|8) (10|0|1)
- 1:   Testicular neoplasm [HP:0010788] <7>(2|1) (2|0|0)
- 1:   Abnormality of the Leydig cells [HP:0010789] <3>(0|0) (0|0|0)
- 1:   Abnormality of the testis size [HP:0045058] <2>(0|1) (0|0|0)
- 1:   Cryptorchidism [HP:0000028] <2>(5|5) (5|0|0)
- 1:   Anorchism [HP:0030869](0|0) (0|0|0)
- 1:   Dysplastic testes [HP:0008733](0|0) (0|0|0)
- 1:   Hydrocele testis [HP:0000034](0|0) (0|0|0)
- 1:   Intratesticular abscess [HP:0025038](0|0) (0|0|0)
- 1:   Monorchism [HP:0030868](0|0) (0|0|0)
- 1:   Orchitis [HP:0100796](1|0) (1|0|0)
- 1:   Primary testicular failure [HP:0008720](0|0) (0|0|0)
- 1:   Retractile testis [HP:0012646](0|0) (0|0|0)
- 1:   Supernumerary testes [HP:0010470](0|0) (0|0|0)
- 1:   Testicular atrophy [HP:0000029](0|0) (0|0|0)
- 1:   Testicular dysgenesis [HP:0008715](0|0) (0|0|0)
- 1:   Testicular fibrosis [HP:0012860](0|0) (0|0|0)
- 1:   Testicular lipomatosis [HP:0025476](0|0) (0|0|0)
- 1:   Testicular mass [HP:0032404](0|0) (0|0|0)
- 1:   Testicular microlithiasis [HP:0012215](0|0) (0|0|0)
- 1:   Testicular torsion [HP:0100813](0|0) (0|0|0)
- 1:   Vanishing testis [HP:0012870](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
SET domain0.000001735Direct
ARID-like0.0006704Direct
Bromodomain0.001555Inherited
Clavaminate synthase-like0.003517Inherited
FYVE/PHD zinc finger0.2069Inherited
Nuclear receptor ligand-binding domain0.5572Inherited
DEATH domain0.6863Inherited
Glucocorticoid receptor-like (DNA-binding domain)0.7217Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
Histone lysine methyltransferases0.00002314Direct
ARID domain0.0003726Direct
HMG-box0.0006467Direct
Bromodomain0.000904Direct
RecA protein-like (ATPase-domain)0.06581Inherited
PHD domain0.1865Inherited
Nuclear receptor ligand-binding domain0.5085Inherited


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)
Smc hinge domain0Direct
SET domain0.0000006984Direct
ARID-like0.0003448Direct
HMG-box0.0006001Direct
Bromodomain0.0008522Direct
Clavaminate synthase-like0.002067Inherited
FYVE/PHD zinc finger0.1737Inherited
Nuclear receptor ligand-binding domain0.5136Inherited
DEATH domain0.647Inherited
Glucocorticoid receptor-like (DNA-binding domain)0.6834Inherited

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0009409Direct


    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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