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Mammalian Phenotype (MP): abnormal craniofacial development

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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term (+ for parents, - for children) MP term [MP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   craniofacial phenotype [MP:0005382] <1>(20|36) (24|17|10)
+ 1:   abnormal craniofacial morphology [MP:0000428] <5>(20|36) (24|17|10)
0:   abnormal craniofacial development [MP:0003935] <17>(3|3) (5|3|2)
- 1:   abnormal pharyngeal arch morphology [MP:0002884] <11>(0|0) (1|1|0)
- 1:   abnormal tooth development [MP:0000116] <8>(0|0) (0|0|0)
- 1:   abnormal Meckel's cartilage morphology [MP:0005587] <3>(1|1) (1|0|0)
- 1:   abnormal palate development [MP:0009653] <2>(3|3) (3|0|1)
- 1:   abnormal Reichert's cartilage morphology [MP:0004915] <1>(0|0) (0|0|0)
- 1:   abnormal frontonasal prominence morphology [MP:0009901] <1>(0|0) (0|0|0)
- 1:   abnormal nasal capsule morphology [MP:0004726] <1>(1|1) (1|0|0)
- 1:   abnormal nasal placode morphology [MP:0006292] <1>(0|0) (0|0|0)
- 1:   abnormal lateral nasal prominence morphology [MP:0009902](0|0) (0|0|0)
- 1:   abnormal mandibular prominence morphology [MP:0010939](0|0) (0|0|0)
- 1:   abnormal maxillary prominence morphology [MP:0010940](0|0) (0|0|0)
- 1:   abnormal medial nasal prominence morphology [MP:0009903](0|0) (0|0|0)
- 1:   abnormal nasal pit morphology [MP:0006306](0|0) (0|0|0)
- 1:   abnormal optic pit morphology [MP:0012155](0|0) (0|0|0)
- 1:   abnormal otic pit morphology [MP:0011172](0|0) (0|0|0)
- 1:   abnormal otic placode morphology [MP:0011173](0|0) (0|0|0)
- 1:   craniofacial asymmetry [MP:0008863](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain-like0.001824Inherited
FnI-like domain0.1535Inherited
p53-like transcription factors0.4369Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain0.002026Inherited
VWC domain0.02371Inherited
T-box0.2112Inherited


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)
Orange domain-like0.0009114Direct
Homeodomain-like0.001032Inherited
FnI-like domain0.1218Inherited
Snake toxin-like0.1255Inherited
p53-like transcription factors0.3895Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
141072,141072
  • 141072 - CalX-like
  • 141072 - CalX-like
  • 0.0004649Direct
    47459,158457
  • 47459 - HLH, helix-loop-helix DNA-binding domain
  • 158457 - Orange domain-like
  • 0.0009114Direct
    57716,48508
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 48508 - Nuclear receptor ligand-binding domain
  • 0.07032Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57603,57603,57603
  • 57603 - FnI-like domain
  • 57603 - FnI-like domain
  • 57603 - FnI-like domain
  • 0.0004649Direct
    48726,48726,48726
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 0.3947Inherited


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