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Mammalian Phenotype (MP): decreased thymocyte number

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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)
+ + + + + + 6:   abnormal immune system cell morphology [MP:0000716] <5>(38|63) (48|29|16)
+ + + + + + 6:   abnormal hematopoietic cell morphology [MP:0013656] <9>(49|77) (60|43|18)
+ + + + + 5:   abnormal hematopoietic cell number [MP:0011180] <7>(34|57) (43|29|13)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   abnormal leukocyte morphology [MP:0008246] <4>(37|62) (47|29|15)
+ + + + + 5:   abnormal mononuclear cell morphology [MP:0008247] <2>(34|57) (41|28|14)
+ + + + 4:   endocrine/exocrine gland phenotype [MP:0005379] <2>(51|81) (55|36|12)
+ + + + 4:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + + 4:   abnormal leukocyte cell number [MP:0000217] <8>(29|49) (37|25|12)
+ + + + 4:   abnormal lymphocyte morphology [MP:0002619] <5>(28|46) (33|26|14)
+ + + + 4:   decreased hematopoietic cell number [MP:0011182] <5>(21|34) (27|21|11)
+ + + 3:   abnormal gland morphology [MP:0002163] <8>(44|71) (50|31|11)
+ + + 3:   abnormal immune system morphology [MP:0000685] <3>(51|76) (60|35|18)
+ + + 3:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + 3:   abnormal T cell morphology [MP:0008037] <9>(14|25) (18|19|11)
+ + + 3:   abnormal lymphocyte cell number [MP:0000717] <6>(18|38) (25|21|9)
+ + + 3:   decreased leukocyte cell number [MP:0000221] <5>(17|28) (24|18|10)
+ + 2:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ + 2:   abnormal endocrine gland morphology [MP:0013560] <7>(16|29) (21|19|4)
+ + 2:   decreased lymphocyte cell number [MP:0005016] <5>(16|28) (22|16|7)
+ + 2:   abnormal T cell number [MP:0006387] <11>(8|22) (16|15|7)
+ + 2:   abnormal immune system organ morphology [MP:0002722] <8>(21|31) (26|15|9)
+ 1:   decreased T cell number [MP:0005018] <12>(8|15) (13|11|5)
+ 1:   abnormal thymus morphology [MP:0000703] <14>(10|16) (12|10|2)
0:   decreased thymocyte number [MP:0000715] <4>(2|4) (4|2|1)
- 1:   decreased DN1 thymic pro-T cell number [MP:0010130](0|0) (0|0|0)
- 1:   decreased DN2 thymocyte number [MP:0010132](0|0) (1|1|0)
- 1:   decreased DN3 thymocyte number [MP:0010134](0|0) (0|0|0)
- 1:   decreased DN4 thymocyte number [MP:0010136](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
SH2 domain0.0003962Direct
Cysteine-rich domain0.0004003Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Pointed domain0.0001096Direct
SH2 domain0.0002064Direct
ets domain0.0006206Direct
Protein kinase cysteine-rich domain (cys2, phorbol-binding domain)0.0007655Direct


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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)
SH2 domain0.0002069Direct
Cysteine-rich domain0.0002089Direct
Protein kinase-like (PK-like)0.0005522Direct
beta-beta-alpha zinc fingers0.2391Inherited

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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
    57667,57667
  • 57667 - beta-beta-alpha zinc fingers
  • 57667 - beta-beta-alpha zinc fingers
  • 0.2197Inherited

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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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