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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 skin morphology
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Accession:MP:0002060 term browser browse the term
Definition:any structural anomaly of the membranous protective covering of the body
Synonyms:exact_synonym: abnormal cutis morphology;   abnormal skin anatomy;   skin dysplasia
 xref: Fyler:4133


show annotations for term's descendants           Sort by:
 
absent Meibomian glands term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Edaradd EDAR-associated death domain IAGP DNA:missense mutation:exon:p.Pro153Ser(rat) RGD PMID:22013926 RGD:14398762 NCBI chr17:90,802,280...90,843,476
Ensembl chr17:90,802,393...90,843,485
JBrowse link
G EdaraddswhKyo EDAR-associated death domain;swh Kyo mutant IAGP DNA:missense mutation:exon:p.Pro153Ser(rat) RGD PMID:22013926 RGD:14398762
decreased skin pigmentation term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Aire autoimmune regulator IMP RGD PMID:29959280 RGD:38599145 NCBI chr20:11,365,630...11,380,636
Ensembl chr20:11,365,697...11,380,631
JBrowse link
G Aireem1Ang autoimmune regulator; ZFN induced mutant1, Ang IMP RGD PMID:29959280 RGD:38599145
variable depigmentation term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Aire autoimmune regulator IMP RGD PMID:29959280 RGD:38599145 NCBI chr20:11,365,630...11,380,636
Ensembl chr20:11,365,697...11,380,631
JBrowse link
G Aireem1Ang autoimmune regulator; ZFN induced mutant1, Ang IMP RGD PMID:29959280 RGD:38599145

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 4987
    integument phenotype 164
      abnormal skin morphology 8
        abnormal cutaneous collagen fibril morphology 0
        abnormal cutaneous elastic fiber morphology + 0
        abnormal dermal layer morphology + 3
        abnormal epidermal layer morphology + 0
        abnormal epidermal-dermal junction morphology + 0
        abnormal head skin morphology + 0
        abnormal neck skin morphology + 0
        abnormal skin appearance + 1
        abnormal skin cell number + 0
        abnormal skin coloration + 4
        abnormal skin condition + 0
        abnormal skin development + 0
        calcified skin 0
        decreased skin tumor incidence 0
        dyskeratosis 0
        increased skin tumor incidence + 0
        skin atrophy + 0
        skin fibrosis 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.