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Mammalian Phenotype (MP): abnormal coat/hair pigmentation

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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)
+ + + + 4:   integument phenotype [MP:0010771] <5>(46|64) (53|34|18)
+ + + 3:   abnormal skin adnexa morphology [MP:0010678] <12>(21|28) (23|21|10)
+ + 2:   abnormal coat/ hair morphology [MP:0000367] <7>(8|9) (10|5|4)
+ + 2:   mammalian phenotype [MP:0000001] <29>
+ 1:   abnormal coat appearance [MP:0001510] <11>(8|9) (10|5|4)
+ 1:   pigmentation phenotype [MP:0001186] <13>(4|5) (6|1|3)
0:   abnormal coat/hair pigmentation [MP:0002075] <20>(3|3) (3|0|2)
- 1:   abnormal hair follicle melanocyte morphology [MP:0004381] <3>(0|0) (0|0|0)
- 1:   abnormal hair shaft melanin granule morphology [MP:0008731] <3>(0|0) (0|0|0)
- 1:   white spotting [MP:0002938] <3>(0|1) (0|0|0)
- 1:   abnormal agouti pigmentation [MP:0012076] <2>(0|0) (0|0|0)
- 1:   irregular coat pigmentation [MP:0000372] <2>(0|0) (0|0|0)
- 1:   abnormal dorsoventral coat patterning [MP:0008238](0|0) (0|0|0)
- 1:   abnormal flank coat pigmentation [MP:0011280](0|0) (0|0|0)
- 1:   abnormal hair follicle melanogenesis [MP:0004382](0|0) (0|0|0)
- 1:   abnormal hind foot hair pigmentation [MP:0009934](0|0) (0|0|0)
- 1:   abnormal pinna hair pigmentation [MP:0009928](0|0) (0|0|0)
- 1:   abnormal rostrocaudal coat patterning [MP:0008812](0|0) (0|0|0)
- 1:   abnormal tail hair pigmentation [MP:0009933](0|0) (0|0|0)
- 1:   abnormal ventral coat pigmentation [MP:0008237](0|0) (0|0|0)
- 1:   absent coat pigmentation [MP:0005171](1|1) (1|0|0)
- 1:   belly blaze [MP:0004034](0|0) (0|0|0)
- 1:   belted [MP:0002671](0|0) (0|0|0)
- 1:   black belted [MP:0020235](0|0) (0|0|0)
- 1:   diluted coat color [MP:0000371](2|1) (2|0|2)
- 1:   grizzled coat color [MP:0012017](0|0) (0|0|0)
- 1:   head blaze [MP:0000370](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)
Di-copper centre-containing domain0Direct
Frizzled cysteine-rich domain0.04742Inherited
HLH, helix-loop-helix DNA-binding domain0.2996Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Paired domain0.02385Inherited
Frizzled cysteine-rich domain0.02833Inherited
HLH, helix-loop-helix DNA-binding domain0.2202Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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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)
Di-copper centre-containing domain0Direct
Frizzled cysteine-rich domain0.03342Inherited
HLH, helix-loop-helix DNA-binding domain0.2564Inherited

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57184,57196,57196
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.02718Inherited
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.02718Inherited


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