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Phenotypic Abnormality (PA): Abnormal retinal morphology

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

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> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + + 3:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ + 2:   Abnormal posterior eye segment morphology [HP:0004329] <3>(16|11) (17|6|8)
+ 1:   Abnormal fundus morphology [HP:0001098] <10>(15|11) (16|6|8)
0:   Abnormal retinal morphology [HP:0000479] <27>(11|6) (12|5|8)
- 1:   Abnormal retinal vascular morphology [HP:0008046] <15>(2|1) (2|2|1)
- 1:   Abnormal macular morphology [HP:0001103] <14>(2|0) (1|0|1)
- 1:   Yellow/white lesions of the retina [HP:0030506] <9>(1|2) (2|1|1)
- 1:   Abnormal chorioretinal morphology [HP:0000532] <8>(2|1) (3|1|2)
- 1:   Retinal dystrophy [HP:0000556] <7>(4|1) (4|2|1)
- 1:   Retinal detachment [HP:0000541] <5>(1|1) (2|0|0)
- 1:   Retinal hamartoma [HP:0009594] <5>(0|0) (0|0|0)
- 1:   Retinal hemorrhage [HP:0000573] <5>(0|0) (0|0|0)
- 1:   Retinal degeneration [HP:0000546] <4>(1|0) (1|0|1)
- 1:   Aplasia/Hypoplasia of the retina [HP:0008061] <3>(0|0) (0|0|0)
- 1:   Abnormal retinal nerve fiber layer morphology [HP:0020119] <2>(0|0) (0|0|0)
- 1:   Abnormality of retinal pigmentation [HP:0007703] <2>(2|2) (2|3|1)
- 1:   Retinal coloboma [HP:0000480] <2>(0|0) (0|0|0)
- 1:   Retinal perforation [HP:0011958] <2>(0|0) (0|0|0)
- 1:   Sub-RPE deposits [HP:0031531] <2>(0|0) (0|0|0)
- 1:   Subretinal deposits [HP:0031528] <2>(0|0) (0|0|0)
- 1:   Retinal fold [HP:0008052] <1>(0|0) (0|0|0)
- 1:   Retinal neoplasm [HP:0012777] <1>(0|0) (0|0|0)
- 1:   Retinopathy [HP:0000488] <1>(0|0) (0|0|0)
- 1:   Retinoschisis [HP:0030502] <1>(0|0) (0|0|0)
- 1:   Angioid streaks of the fundus [HP:0001102](0|0) (0|0|0)
- 1:   Intraretinal fluid [HP:0031527](0|0) (0|0|0)
- 1:   Retinal dysplasia [HP:0007973](1|0) (1|0|0)
- 1:   Retinal infarction [HP:0007866](0|0) (0|0|0)
- 1:   Retinal thinning [HP:0030329](0|0) (0|0|0)
- 1:   Retinitis [HP:0032118](0|0) (0|0|0)
- 1:   Subretinal fluid [HP:0031526](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)
GroEL equatorial domain-like0.002393Inherited
GAF domain-like0.009306Inherited
GroEL apical domain-like0.02682Inherited
SCOP hierarchy in SUPERFAMILY0.09295Inherited
FnI-like domain0.1109Inherited
Voltage-gated potassium channels0.1894Inherited
RING/U-box0.2907Inherited
Growth factor receptor domain0.3933Inherited
Complement control module/SCR domain0.4578Inherited
Nucleotide-diphospho-sugar transferases0.7061Inherited
(Trans)glycosidases0.7429Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
GAF domain0.005658Inherited
VWC domain0.01208Inherited
EGF-type module0.07205Inherited
Laminin G-like module0.08378Inherited
Complement control module/SCR domain0.403Inherited
LDL receptor-like module0.5148Inherited


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)
GroEL equatorial domain-like0.001361Inherited
GAF domain-like0.005957Inherited
GroEL apical domain-like0.01864Inherited
FnI-like domain0.08754Inherited
Voltage-gated potassium channels0.1575Inherited
RING/U-box0.2513Inherited
Growth factor receptor domain0.3499Inherited
EGF/Laminin0.3721Inherited
Complement control module/SCR domain0.4139Inherited
LDL receptor-like module0.5055Inherited
Nucleotide-diphospho-sugar transferases0.6672Inherited
(Trans)glycosidases0.7053Inherited

(show details)
Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.001079Inherited
    55781,109604
  • 55781 - GAF domain-like
  • 109604 - HD-domain/PDEase-like
  • 0.005957Inherited
    55781,55781
  • 55781 - GAF domain-like
  • 55781 - GAF domain-like
  • 0.005957Inherited
    49899,49899
  • 49899 - Concanavalin A-like lectins/glucanases
  • 49899 - Concanavalin A-like lectins/glucanases
  • 0.05082Inherited
    57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.4974Inherited

    (show details)
    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57581,57196
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 57196 - EGF/Laminin
  • 0Direct
    57196,57196,57581
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 0Direct
    57196,57581,57184
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 57184 - Growth factor receptor domain
  • 0Direct
    57184,57196,57196
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0003337Direct
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.005351Inherited
    55781,55781,109604
  • 55781 - GAF domain-like
  • 55781 - GAF domain-like
  • 109604 - HD-domain/PDEase-like
  • 0.005957Inherited
    57535,57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.1642Inherited
    57196,57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.2043Inherited


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