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Mammalian Phenotype (MP): spontaneous chromosome breakage

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

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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + + 4:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + + 3:   abnormal chromosome stability [MP:0010094] <2>(6|6) (6|2|0)
+ + 2:   chromosomal instability [MP:0008866] <1>(6|6) (6|2|0)
+ 1:   chromosome breakage [MP:0004028] <2>(1|2) (1|2|0)
0:   spontaneous chromosome breakage [MP:0004029](0|1) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
DNA replication initiator (cdc21/cdc54) N-terminal domain0.0000002449Direct


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