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Symbol
Name
ID

Carmil2
capping protein regulator and myosin 1 linker 2
MGI:2685431

Phenotype annotations related to integument

Darker colors indicate more annotations

Human Phenotypes

Cold urticaria

Cutaneous abscess

Recurrent cutaneous abscess formation

Eczematoid dermatitis

Seborrheic dermatitis

Chronic mucocutaneous candidiasis

Molluscum contagiosum

Scaling skin

Psoriasiform lesion

Cutaneous photosensitivity

Atrophic scars

Ichthyosis

Verrucae

Disease(s) Associated with CARMIL2

immunodeficiency 58

Mouse Phenotypes		abnormal coat/hair pigmentation
Availability	Mouse Genotype	abnormal coat/hair pigmentation
	Carmil2^{tm1b(KOMP)Mbp}/Carmil2^{tm1b(KOMP)Mbp}

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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