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Mammalian Phenotype (MP): abnormal transitional stage T2 B cell 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)
+ + + + + + + + + + + + 12:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + + + 9:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + + + + + + 8:   abnormal blood cell morphology/development [MP:0002429] <3>(26|35) (28|24|9)
+ + + + + + + + 8:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ + + + + + + + 8:   abnormal blood cell morphology [MP:0013657] <4>(31|49) (37|35|14)
+ + + + + + + + 8:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + + + + + 7:   abnormal immune system morphology [MP:0000685] <3>(50|76) (60|35|18)
+ + + + + + + 7:   abnormal hemopoiesis [MP:0013693] <2>(25|34) (27|24|9)
+ + + + + + + 7:   abnormal hematopoietic cell morphology [MP:0013656] <9>(49|76) (60|43|18)
+ + + + + + 6:   abnormal definitive hematopoiesis [MP:0002123] <4>(24|34) (26|24|9)
+ + + + + + 6:   abnormal leukocyte morphology [MP:0008246] <4>(36|61) (47|29|15)
+ + + + + + 6:   abnormal immune system cell morphology [MP:0000716] <5>(37|62) (48|29|16)
+ + + + + 5:   abnormal leukopoiesis [MP:0005460] <3>(17|28) (21|18|8)
+ + + + + 5:   abnormal mononuclear cell morphology [MP:0008247] <2>(33|56) (41|28|14)
+ + + + 4:   abnormal lymphocyte morphology [MP:0002619] <5>(27|45) (33|26|14)
+ + + + 4:   abnormal lymphopoiesis [MP:0002401] <3>(17|25) (21|15|6)
+ + + 3:   abnormal B cell differentiation [MP:0002144] <10>(12|17) (13|8|2)
+ + + 3:   abnormal B cell morphology [MP:0004939] <6>(17|27) (20|11|6)
+ + 2:   abnormal immature B cell morphology [MP:0005022] <2>(4|8) (4|6|1)
+ 1:   abnormal transitional stage B cell morphology [MP:0008188] <5>(2|4) (2|3|1)
0:   abnormal transitional stage T2 B cell morphology [MP:0009920] <2>(2|2) (2|3|1)
- 1:   decreased transitional stage T2 B cell number [MP:0009926] <1>(2|2) (2|2|1)
- 1:   increased transitional stage T2 B cell number [MP:0009925](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
DBL homology domain (DH-domain)0.00001119Direct
Calponin-homology domain, CH-domain0.0002205Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
DBL homology domain (DH-domain)0.000003365Direct
Calponin-homology domain, CH-domain0.00008151Direct


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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)
DBL homology domain (DH-domain)0.000004932Direct
Calponin-homology domain, CH-domain0.0001118Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
47576,48065
  • 47576 - Calponin-homology domain, CH-domain
  • 48065 - DBL homology domain (DH-domain)
  • 0Direct
    55550,50044
  • 55550 - SH2 domain
  • 50044 - SH3-domain
  • 0.0000000006913Direct
    48065,50729
  • 48065 - DBL homology domain (DH-domain)
  • 50729 - PH domain-like
  • 0.000003981Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    47576,48065,50729
  • 47576 - Calponin-homology domain, CH-domain
  • 48065 - DBL homology domain (DH-domain)
  • 50729 - PH domain-like
  • 0Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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