abnormal hypodermis morphology - Ontology Report - Rat Genome Database

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MAMMALIAN PHENOTYPE - ANNOTATIONS	{{ watchLinkText }}
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 hypodermis morphology	go back to main search page
Accession:	MP:0003705	browse the term
Definition:	any structural anomaly of the irregular layer of loose connective tissue containing fibroblasts, adipose cells, and macrophages, that is immediately deep to the skin and superficial to the deep fascia; usually consisting primarily of a fatty layer and may also include a muscle layer and/or a fibrous layer, or it may occur as a membranous layer only, being nearly devoid of fat; it contains skin ligaments extending between the dermis and deep fascia, cutaneous nerves, and superficial vessels, with terminal branches passing into the skin layers
Synonyms:	exact_synonym:	abnormal stratum subcutaneum morphology; abnormal subcutaneous tissue morphology; abnormal subcutis morphology; abnormal superficial fascia morphology; abnormal tela subcutanea morphology; hypodermal dysplasia
	related_synonym:	abnormal hypoderm morphology

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Rat (9) Mouse (234) Human (0) Chinchilla (0) Bonobo (0) Dog (0) Squirrel (0) Pig (0) Green Monkey (0) Naked Mole-rat (0) All
Genes (4) Strains (5)

increased subcutaneous adipose tissue amount

term browser

Symbol

Object Name

Evidence

Notes

Source

PubMed Reference(s)

RGD Reference(s)

Position

G

complement factor B

compared to wild type SHR

RGD

NCBI chr20:3,970,643...3,976,510
Ensembl chr20:3,951,474...3,976,505

G

complement factor B, ZFN induced mutant 1, Tja

compared to wild type SHR

RGD

G

melanocortin 4 receptor

RGD

NCBI chr18:60,419,832...60,421,719
Ensembl chr18:60,419,832...60,421,719

G

melanocortin 4 receptor; ENU induced mutation 1, Hubr

RGD

Term paths to the root

Path 1
Term	Annotations
mammalian phenotype	5375
integument phenotype	168
abnormal skin adnexa morphology	166
abnormal hypodermis morphology	9
abnormal hypodermis fat layer morphology +	9
abnormal hypodermis muscle layer morphology +	0
increased hypodermis neovascularization	0
subcutaneous edema	0
thick hypodermis	0
thin hypodermis	0

paths to the root