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Phenotypic Abnormality (PA): Abnormality of urine homeostasis

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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)
+ + + 3:   Abnormality of the genitourinary system [HP:0000119] <5>(72|74) (80|28|7)
+ + 2:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the urinary system [HP:0000079] <4>(36|39) (42|14|6)
+ 1:   Abnormality of metabolism/homeostasis [HP:0001939] <15>(73|82) (83|38|18)
+ 1:   Abnormality of the urinary system physiology [HP:0011277] <3>(21|24) (25|8|4)
0:   Abnormality of urine homeostasis [HP:0003110] <57>(14|16) (18|3|0)
- 1:   Abnormal urine carbohydrate level [HP:0031979] <12>(0|0) (0|0|0)
- 1:   Abnormal urinary color [HP:0012086] <9>(0|0) (0|0|0)
- 1:   Proteinuria [HP:0000093] <9>(0|0) (0|0|0)
- 1:   Abnormal urinary electrolyte concentration [HP:0012591] <7>(1|3) (4|1|0)
- 1:   Abnormal urine carboxylic acid level [HP:0031980] <5>(0|0) (0|0|0)
- 1:   Abnormal urine cytology [HP:0012614] <4>(2|3) (2|1|0)
- 1:   Aciduria [HP:0012072] <3>(8|7) (8|1|0)
- 1:   Abnormal urinary 1-methylhistidine concentration [HP:0410313] <2>(0|0) (0|0|0)
- 1:   Abnormal urinary 3-methylhistidine concentration [HP:0410316] <2>(0|0) (0|0|0)
- 1:   Abnormal urinary mineral level [HP:0025640] <2>(0|0) (0|0|0)
- 1:   Abnormal urinary sulfate concentration [HP:0012612] <2>(0|0) (0|0|0)
- 1:   Abnormal urine alpha-ketoglutarate concentration [HP:0012401] <2>(0|0) (0|0|0)
- 1:   Abnormal urine citrate concentration [HP:0012404] <2>(0|0) (0|0|0)
- 1:   Abnormal urine urobilinogen level [HP:0032472] <2>(0|0) (0|0|0)
- 1:   Abnormality of urinary uric acid concentration [HP:0012610] <2>(0|0) (0|0|0)
- 1:   Abnormality of urine bicarbonate concentration [HP:0011279] <2>(0|0) (0|0|0)
- 1:   Abnormality of urine catecholamine concentration [HP:0011281] <2>(0|0) (0|0|0)
- 1:   Crystalluria [HP:0020074] <2>(0|0) (0|0|0)
- 1:   Glycopeptiduria [HP:0012067] <2>(0|0) (0|0|0)
- 1:   Myoglobinuria [HP:0002913] <2>(0|0) (0|0|0)
- 1:   Abnormal urinary acylglycine profile [HP:0012073] <1>(0|0) (0|0|0)
- 1:   Abnormal urine hexanoylglycine concentration [HP:0500254] <1>(0|0) (0|0|0)
- 1:   Abnormal urine sebacic acid concentration [HP:0500251] <1>(0|0) (0|0|0)
- 1:   Abnormality of urine glucose concentration [HP:0011016] <1>(0|0) (0|0|0)
- 1:   Hemoglobinuria [HP:0003641] <1>(0|0) (0|0|0)
- 1:   Urinary glycosaminoglycan excretion [HP:0003541] <1>(2|1) (2|0|0)
- 1:   Abnormal concentration of acylcarnitine in the urine [HP:0500170](0|0) (0|0|0)
- 1:   Abnormal urinary odor [HP:0012088](0|0) (0|0|0)
- 1:   Absent urinary urothione [HP:0003606](0|0) (0|0|0)
- 1:   Bacteriuria [HP:0012461](0|0) (0|0|0)
- 1:   Bilirubinuria [HP:0031811](0|0) (0|0|0)
- 1:   Cloudy urine [HP:0031967](0|0) (0|0|0)
- 1:   Elevated urinary N-acetylaspartic acid level [HP:0032272](0|0) (0|0|0)
- 1:   Elevated urinary delta-aminolevulinic acid [HP:0003163](0|0) (0|0|0)
- 1:   Elevated urine pyrophosphate [HP:0003491](0|0) (0|0|0)
- 1:   Foamy urine [HP:0031504](0|0) (0|0|0)
- 1:   Hemosiderinuria [HP:0012543](0|0) (0|0|0)
- 1:   Hyperprostaglandinuria [HP:0003527](0|0) (0|0|0)
- 1:   Hyperuricosuria [HP:0003149](0|0) (0|0|0)
- 1:   Hyposthenuria [HP:0003158](0|0) (0|0|0)
- 1:   Increased level of N-acetylneuraminic acid in urine [HP:0410156](0|0) (0|0|0)
- 1:   Increased level of O-phosphoethanolamine in urine [HP:0410158](0|0) (0|0|0)
- 1:   Increased urinary excretion of galactosyl hydroxylysine [HP:0031991](0|0) (0|0|0)
- 1:   Increased urinary hypoxanthine [HP:0011814](0|0) (0|0|0)
- 1:   Increased urinary mucus [HP:0032068](0|0) (0|0|0)
- 1:   Increased urinary porphobilinogen [HP:0012217](0|0) (0|0|0)
- 1:   Increased urinary sulfite [HP:0011942](0|0) (0|0|0)
- 1:   Increased urinary thiosulfate [HP:0011943](0|0) (0|0|0)
- 1:   Increased urinary type 1 collagen N-terminal telopeptide level [HP:0032208](0|0) (0|0|0)
- 1:   Ketonuria [HP:0002919](0|0) (0|0|0)
- 1:   Low urinary cyclic AMP response to PTH administration [HP:0003456](0|0) (0|0|0)
- 1:   Nitrituria [HP:0031812](0|0) (0|0|0)
- 1:   Parathormone-independent increased renal tubular calcium reabsorption [HP:0003529](0|0) (0|0|0)
- 1:   Porphyrinuria [HP:0010473](0|0) (0|0|0)
- 1:   Trimethylaminuria [HP:0003614](0|0) (0|0|0)
- 1:   Uraciluria [HP:0012127](0|0) (0|0|0)
- 1:   Xanthinuria [HP:0010934](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
PRTase-like0Direct
L-aspartase-like0.004316Inherited
ClpP/crotonase0.007011Inherited
Adenine nucleotide alpha hydrolases-like0.01291Inherited
(Trans)glycosidases0.01601Inherited
Acyl-CoA dehydrogenase NM domain-like0.01672Inherited
Alkaline phosphatase-like0.01672Inherited
Acyl-CoA dehydrogenase C-terminal domain-like0.01672Inherited
Glutathione synthetase ATP-binding domain-like0.01693Inherited
PreATP-grasp domain0.03835Inherited
Clc chloride channel0.08332Inherited
Mitochondrial carrier0.1022Inherited
C-type lectin-like0.1169Inherited
L domain-like0.4611Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
beta-glycanases0Direct
Phosphoribosyltransferases (PRTases)0Direct
HCDH C-domain-like0Direct
Medium chain acyl-CoA dehydrogenase, NM (N-terminal and middle) domains0.002164Inherited
Medium chain acyl-CoA dehydrogenase-like, C-terminal domain0.002164Inherited
Noncollagenous (NC1) domain of collagen IV0.002511Inherited
Cytoplasmic domain of inward rectifier potassium channel0.003594Inherited
Arylsulfatase0.01391Inherited
Crotonase-like0.02675Inherited
Cystathionine synthase-like0.02675Inherited
BC N-terminal domain-like0.07346Inherited
BC ATP-binding domain-like0.07346Inherited
Clc chloride channel0.07346Inherited
Cytochrome P4500.0942Inherited
Mitochondrial carrier0.09471Inherited
Ngr ectodomain-like0.2866Inherited


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)
PRTase-like0Direct
Integrin domains0.0009617Direct
L-aspartase-like0.002651Inherited
ClpP/crotonase0.0045Inherited
Adenine nucleotide alpha hydrolases-like0.008584Inherited
(Trans)glycosidases0.01082Inherited
Acyl-CoA dehydrogenase NM domain-like0.01134Inherited
Acyl-CoA dehydrogenase C-terminal domain-like0.01134Inherited
Alkaline phosphatase-like0.01134Inherited
Glutathione synthetase ATP-binding domain-like0.01151Inherited
CBS-domain pair0.02709Inherited
PreATP-grasp domain0.02794Inherited
Clc chloride channel0.06506Inherited
Mitochondrial carrier0.08101Inherited
C-type lectin-like0.09366Inherited
Cytochrome P4500.107Inherited
L domain-like0.4187Inherited
Voltage-gated potassium channels0.8135Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
81324,81296
  • 81324 - Voltage-gated potassium channels
  • 81296 - E set domains
  • 0.002801Inherited
    56436,56436
  • 56436 - C-type lectin-like
  • 56436 - C-type lectin-like
  • 0.0103Inherited
    56645,47203
  • 56645 - Acyl-CoA dehydrogenase NM domain-like
  • 47203 - Acyl-CoA dehydrogenase C-terminal domain-like
  • 0.01134Inherited


    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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