disheveled coat Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description coat that looks generally unkempt (Mammalian Phenotype Ontology, MP_0001511)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001511
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Genes

39 gene mutations causing the disheveled coat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
A2M alpha-2-macroglobulin
AARS alanyl-tRNA synthetase
AGA aspartylglucosaminidase
APRT adenine phosphoribosyltransferase
ATP7B ATPase, Cu++ transporting, beta polypeptide
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
BARX2 BARX homeobox 2
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CHD2 chromodomain helicase DNA binding protein 2
CTSA cathepsin A
CTSC cathepsin C
DCR Down syndrome chromosome region
DRD1 dopamine receptor D1
DSC1 desmocollin 1
FGF7 fibroblast growth factor 7
IDUA iduronidase, alpha-L-
IFT88 intraflagellar transport 88
JAM3 junctional adhesion molecule 3
KRT31 keratin 31, type I
LACTB2 lactamase, beta 2
LMNA lamin A/C
LPIN1 lipin 1
MAPT microtubule-associated protein tau
MECP2 methyl CpG binding protein 2
MPZL3 myelin protein zero-like 3
NAGLU N-acetylglucosaminidase, alpha
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
NSDHL NAD(P) dependent steroid dehydrogenase-like
PKP3 plakophilin 3
PRSS8 protease, serine, 8
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
RELN reelin
SGSH N-sulfoglucosamine sulfohydrolase
SNAP25 synaptosomal-associated protein, 25kDa
SOX18 SRY (sex determining region Y)-box 18
TBK1 TANK-binding kinase 1
TGFA transforming growth factor, alpha
TGFB1 transforming growth factor, beta 1
TPP2 tripeptidyl peptidase II