thick skin Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater thickness of the outer protective layer of the body (Mammalian Phenotype Ontology, MP_0001200)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001200
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Genes

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

Symbol Name
AHR aryl hydrocarbon receptor
CHUK conserved helix-loop-helix ubiquitous kinase
COL1A1 collagen, type I, alpha 1
CST6 cystatin E/M
CTSV cathepsin V
DSG4 desmoglein 4
ERCC2 excision repair cross-complementation group 2
ERRFI1 ERBB receptor feedback inhibitor 1
FBN1 fibrillin 1
HR hair growth associated
HTT huntingtin
JDP2 Jun dimerization protein 2
KRT16 keratin 16, type I
KRT9 keratin 9, type I
LDLR low density lipoprotein receptor
NFKBIZ nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, zeta
NTF4 neurotrophin 4
RAG1 recombination activating gene 1
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
RIPK4 receptor-interacting serine-threonine kinase 4
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4
UROS uroporphyrinogen III synthase