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Phenotypic Abnormality (PA): Abnormality of the musculature of the upper limbs 

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term
(+ for parents, - for children)
HP term [HP ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + 2:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ + 2:   Abnormality of limbs [HP:0040064] <8>(58|66) (63|33|25)
+ 1:   Abnormality of the upper limb [HP:0002817] <20>(29|35) (35|17|16)
+ 1:   Abnormality of the musculature of the limbs [HP:0009127] <10>(12|11) (16|5|3)
0:   Abnormality of the musculature of the upper limbs [HP:0001446] <8>(6|7) (7|2|1)
- 1:   Abnormality of the musculature of the hand [HP:0001421] <6>(2|2) (2|1|0)
- 1:   Abnormality of the shoulder girdle musculature [HP:0001435] <5>(6|5) (6|1|0)
- 1:   Aplasia/Hypoplasia involving the musculature of the upper limbs [HP:0001467] <3>(0|0) (0|0|0)
- 1:   Abnormality of the musculature of the upper arm [HP:0001457] <2>(0|0) (0|0|0)
- 1:   Upper limb muscle hypertrophy [HP:0040265] <2>(0|0) (0|0|0)
- 1:   Proximal muscle weakness in upper limbs [HP:0008997] <1>(2|2) (2|1|0)
- 1:   Upper limb amyotrophy [HP:0009129] <1>(0|0) (0|0|0)
- 1:   Upper limb hypertonia [HP:0200049](0|0) (0|0|0)

Family

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Family

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SCOP term FDR (all) Annotation (direct or inherited)
Filamin repeat (rod domain)0.00002978Direct
MIR domain0.00068Direct
Calponin-homology domain, CH-domain0.00119Inherited
Tropomyosin0.005546Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.01605Inherited
Nicotinic receptor ligand binding domain-like0.01605Inherited
Myosin rod fragments0.03402Inherited

LINKTO: Domain2BO Download and Domain2BO Algorithm

Supra-domain (Single|Duplex|Triple)

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Supra-domain (Single)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
MIR domain0.0006798Direct
Calponin-homology domain, CH-domain0.00113Inherited
Tropomyosin0.00542Inherited
UDP-Glycosyltransferase/glycogen phosphorylase0.005612Inherited
Nicotinic receptor ligand binding domain-like0.01567Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.01567Inherited
Myosin rod fragments0.03307Inherited

LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm

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Supra-domain (Duplex) in N- to C-terminal order

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
81296,81296
  • 81296 - E set domains
  • 81296 - E set domains
  • 0.00000666Direct
    63712,90112
  • 63712 - Nicotinic receptor ligand binding domain-like
  • 90112 - Neurotransmitter-gated ion-channel transmembrane pore
  • 0.01567Inherited

    LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm

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    Supra-domain (Triple) in N- to C-terminal order

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    81296,81296,81296
  • 81296 - E set domains
  • 81296 - E set domains
  • 81296 - E set domains
  • 0.00000666Direct

    LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm

    Distribution on sTOL

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