reddish skin Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001190
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Genes

28 gene mutations causing the reddish skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ALOX12B arachidonate 12-lipoxygenase, 12R type
CERS3 ceramide synthase 3
CTSE cathepsin E
DGAT1 diacylglycerol O-acyltransferase 1
DSG4 desmoglein 4
E2F2 E2F transcription factor 2
ELOVL1 ELOVL fatty acid elongase 1
ELOVL4 ELOVL fatty acid elongase 4
ERCC2 excision repair cross-complementation group 2
GBA glucosidase, beta, acid
IL36RN interleukin 36 receptor antagonist
IRF2 interferon regulatory factor 2
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KRT10 keratin 10, type I
LAMC2 laminin, gamma 2
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
PKP3 plakophilin 3
PSTPIP2 proline-serine-threonine phosphatase interacting protein 2
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
SHARPIN SHANK-associated RH domain interactor
SOCS3 suppressor of cytokine signaling 3
SPINK5 serine peptidase inhibitor, Kazal type 5
ST14 suppression of tumorigenicity 14 (colon carcinoma)
TGM1 transglutaminase 1
XPA xeroderma pigmentosum, complementation group A