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Phenotypic Abnormality (PA): Abnormal corpus callosum 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)
+ + + + + + + + + 9:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + + 8:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + + + + 7:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + + + + 6:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ + + + + 5:   Abnormality of brain morphology [HP:0012443] <13>(43|63) (53|34|15)
+ + + + 4:   Abnormality of forebrain morphology [HP:0100547] <6>(26|32) (30|18|5)
+ + + 3:   Abnormality of the cerebrum [HP:0002060] <16>(25|31) (29|18|5)
+ + 2:   Abnormality of the cerebral subcortex [HP:0010993] <3>(6|9) (6|2|0)
+ 1:   Abnormality of the cerebral white matter [HP:0002500] <15>(6|7) (6|2|0)
0:   Abnormal corpus callosum morphology [HP:0001273] <7>(5|7) (5|2|0)
- 1:   Aplasia/Hypoplasia of the corpus callosum [HP:0007370] <2>(5|6) (5|2|0)
- 1:   Abnormal length of corpus callosum [HP:0200011] <1>(0|0) (0|0|0)
- 1:   Corpus callosum atrophy [HP:0007371](0|0) (0|0|0)
- 1:   Dysplastic corpus callosum [HP:0006989](0|0) (0|0|0)
- 1:   Lipoma of corpus callosum [HP:0006931](0|0) (0|0|0)
- 1:   Snowball lesion of corpus callosum [HP:0031948](0|0) (0|0|0)
- 1:   Thick corpus callosum [HP:0007074](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Periplasmic binding protein-like II0.001853Inherited
ARID-like0.004481Inherited
Homeodomain-like0.01136Inherited
Nucleotidylyl transferase0.01897Inherited
Class II aaRS and biotin synthetases0.9023Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Phosphate binding protein-like0.0003386Direct
G proteins0.000557Direct
ARID domain0.002379Inherited
Ypt/Rab-GAP domain of gyp1p0.003052Inherited
Class I aminoacyl-tRNA synthetases (RS), catalytic domain0.01018Inherited
Homeodomain0.03448Inherited
Class II aminoacyl-tRNA synthetase (aaRS)-like, catalytic domain0.4031Inherited


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)
Periplasmic binding protein-like II0.001031Inherited
ARID-like0.002693Inherited
Homeodomain-like0.007356Inherited
Nucleotidylyl transferase0.01281Inherited
Class II aaRS and biotin synthetases0.8732Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
50249,55681
  • 50249 - Nucleic acid-binding proteins
  • 55681 - Class II aaRS and biotin synthetases
  • 0.003359Inherited
    55681,52954
  • 55681 - Class II aaRS and biotin synthetases
  • 52954 - Class II aaRS ABD-related
  • 0.00687Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)