spontaneous skin ulceration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description unpredictable appearance of skin lesions, usually with inflammation (Mammalian Phenotype Ontology, MP_0001209)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001209
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Genes

23 gene mutations causing the spontaneous skin ulceration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AHR aryl hydrocarbon receptor
CLIC4 chloride intracellular channel 4
COL5A2 collagen, type V, alpha 2
E2F4 E2F transcription factor 4, p107/p130-binding
ERRFI1 ERBB receptor feedback inhibitor 1
FADS2 fatty acid desaturase 2
FN1 fibronectin 1
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
LAMC2 laminin, gamma 2
MPZL3 myelin protein zero-like 3
NAGLU N-acetylglucosaminidase, alpha
NEIL1 nei endonuclease VIII-like 1 (E. coli)
NFKBIA nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha
NFKBIZ nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, zeta
PLCB3 phospholipase C, beta 3 (phosphatidylinositol-specific)
PSTPIP2 proline-serine-threonine phosphatase interacting protein 2
PTCH2 patched 2
PTPN6 protein tyrosine phosphatase, non-receptor type 6
RBL1 retinoblastoma-like 1
SCD stearoyl-CoA desaturase (delta-9-desaturase)
TOM1L2 target of myb1-like 2 (chicken)
TP63 tumor protein p63