SUPERFAMILY 1.75 HMM library and genome assignments server

Superfamily is undergoing a server migration - you are now browsing on the new server. Please contact us if you experience any problems.

Mammalian Phenotype (MP): absent somites

(show info)

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)
+ + + + + + + 7:   mammalian phenotype [MP:0000001] <29>
+ + + + + + 6:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + + + + 5:   abnormal embryo morphology [MP:0014134] <4>(23|31) (26|14|12)
+ + + + 4:   abnormal embryonic tissue morphology [MP:0002085] <35>(17|21) (19|10|9)
+ + + 3:   abnormal somite development [MP:0001688] <11>(3|5) (3|3|1)
+ + 2:   impaired somite development [MP:0009768] <2>(3|4) (3|3|1)
+ 1:   failure of somite differentiation [MP:0001690] <1>(0|2) (0|0|0)
0:   absent somites [MP:0006386](0|2) (0|0|0)


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

Family

(show details)
SCOP termFDR (all)Annotation (direct or inherited)
C5 cytosine-specific DNA methylase, DCM0.00000003108Direct
Transforming growth factor (TGF)-beta0.0006303Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
(show help)