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Mammalian Phenotype (MP): abnormal blood flow velocity

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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:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + 2:   abnormal cardiovascular system physiology [MP:0001544] <24>(39|45) (46|26|17)
+ 1:   abnormal blood circulation [MP:0002128] <13>(17|22) (20|10|6)
0:   abnormal blood flow velocity [MP:0000233] <2>(2|0) (2|0|0)
- 1:   abnormal coronary flow rate [MP:0003021] <2>(0|0) (0|0|0)
- 1:   abnormal renal plasma flow rate [MP:0005524] <2>(0|0) (0|0|0)


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

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Riboflavin synthase domain-like0.0004928Direct
Ferredoxin reductase-like, C-terminal NADP-linked domain0.0004928Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
Riboflavin synthase domain-like0.0002599Direct
Ferredoxin reductase-like, C-terminal NADP-linked domain0.0002599Direct


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