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Pathways

MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.

Term:abnormal forehead pigmentation
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Accession:MP:0030052 term browser browse the term
Definition:anomaly in the coloration of the skin of the forehead due to changes in the amount, shape, or distribution of cells producing pigment



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decreased forehead pigmentation term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Snai2 snail family zinc finger 2 IAGP MGI PMID:12444107 NCBI chr16:14,523,716...14,527,259
Ensembl chr16:14,523,716...14,527,249
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increased forehead pigmentation term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Apc APC, WNT signaling pathway regulator IAGP MGI PMID:17002498 NCBI chr18:34,353,350...34,455,243
Ensembl chr18:34,353,977...34,455,605
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Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 16475
    pigmentation phenotype 643
      abnormal skin pigmentation 125
        abnormal forehead pigmentation 2
          decreased forehead pigmentation 1
          increased forehead pigmentation 1
Path 2
Term Annotations click to browse term
  mammalian phenotype 16475
    growth/size/body region phenotype 6831
      abnormal head morphology 1315
        abnormal facial morphology 1077
          abnormal forehead morphology 32
            abnormal forehead skin morphology 2
              abnormal forehead pigmentation 2
                decreased forehead pigmentation 1
                increased forehead pigmentation 1
paths to the root