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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>(74|72) (79|29|9)
+ + + + 4:   Abnormality of the genital system [HP:0000078] <3>(34|34) (36|10|3)
+ + + 3:   Abnormal reproductive system morphology [HP:0012243] <10>(27|26) (27|4|1)
+ + 2:   Abnormality of the male genitalia [HP:0010461] <2>(13|10) (14|1|1)
+ + 2:   Abnormal external genitalia [HP:0000811] <7>(14|10) (14|1|1)
+ 1:   Abnormality of male external genitalia [HP:0000032] <9>(12|9) (13|1|1)
0:   Abnormal testis morphology [HP:0000035] <21>(8|7) (8|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>(4|5) (4|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 domain0.000006283Direct
ARID-like0.0006323Direct
Bromodomain0.001446Inherited
FYVE/PHD zinc finger0.2206Inherited
Nuclear receptor ligand-binding domain0.5491Inherited
DEATH domain0.6778Inherited
Glucocorticoid receptor-like (DNA-binding domain)0.7095Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
Histone lysine methyltransferases0.00002163Direct
ARID domain0.000356Direct
Bromodomain0.0008559Direct
RecA protein-like (ATPase-domain)0.06436Inherited
PHD domain0.205Inherited
Nuclear receptor ligand-binding domain0.5043Inherited


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 domain0.000002739Direct
ARID-like0.0003325Direct
Bromodomain0.0008082Direct
FYVE/PHD zinc finger0.1866Inherited
Nuclear receptor ligand-binding domain0.5064Inherited
DEATH domain0.6393Inherited
Glucocorticoid receptor-like (DNA-binding domain)0.6716Inherited

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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
  • 0.0008989Direct


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