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Mammalian Phenotype (MP): abnormal optic tract morphology

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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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + 2:   abnormal brain morphology [MP:0002152] <24>(25|42) (35|24|14)
+ + 2:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ 1:   abnormal nervous system tract morphology [MP:0000778] <8>(5|9) (7|5|4)
+ 1:   abnormal brain white matter morphology [MP:0008026] <6>(3|8) (5|4|3)
0:   abnormal optic tract morphology [MP:0004267] <3>(0|1) (0|1|0)
- 1:   absent optic tract [MP:0001334](0|0) (0|0|0)
- 1:   decreased optic tract size [MP:0012464](0|0) (0|0|0)
- 1:   increased optic tract size [MP:0012463](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Ephrin receptor ligand binding domain0.0009791Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
56112,47769
  • 56112 - Protein kinase-like (PK-like)
  • 47769 - SAM/Pointed domain
  • 0.0008755Direct