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Mammalian Phenotype (MP): abnormal circulating non-HDL phospholipid level

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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)
+ + + + + + + 7:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + + 4:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + + + 4:   abnormal lipid homeostasis [MP:0002118] <9>(25|29) (29|17|10)
+ + + 3:   abnormal blood homeostasis [MP:0009642] <23>(63|82) (70|45|21)
+ + + 3:   abnormal lipid level [MP:0001547] <16>(24|28) (26|16|10)
+ + 2:   abnormal phospholipid level [MP:0004777] <3>(2|1) (2|1|0)
+ + 2:   abnormal circulating lipid level [MP:0003949] <9>(16|23) (19|13|10)
+ 1:   abnormal circulating phospholipid level [MP:0006084] <4>(2|1) (2|1|0)
0:   abnormal circulating non-HDL phospholipid level [MP:0020127] <2>(0|0) (0|0|0)
- 1:   decreased circulating non-HDL phospholipid level [MP:0020129](0|0) (0|0|0)
- 1:   increased circulating non-HDL phospholipid level [MP:0020128](0|0) (0|0|0)