abnormal tail development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the formation of the tail (Mammalian Phenotype Ontology, MP_0006281)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006281
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26 gene mutations causing the abnormal tail development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AXIN1 axin 1
AXIN2 axin 2
BRCA1 breast cancer 1, early onset
BRWD3 bromodomain and WD repeat domain containing 3
CCDC134 coiled-coil domain containing 134
CORO1C coronin, actin binding protein, 1C
CSNK2A1 casein kinase 2, alpha 1 polypeptide
DACT1 dishevelled-binding antagonist of beta-catenin 1
DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1
FGFR1 fibroblast growth factor receptor 1
FN1 fibronectin 1
LMX1A LIM homeobox transcription factor 1, alpha
LRP6 low density lipoprotein receptor-related protein 6
MSGN1 mesogenin 1
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
NR6A1 nuclear receptor subfamily 6, group A, member 1
PALB2 partner and localizer of BRCA2
QKI QKI, KH domain containing, RNA binding
ROR2 receptor tyrosine kinase-like orphan receptor 2
SHB Src homology 2 domain containing adaptor protein B
T T, brachyury homolog (mouse)
TBX6 T-box 6
TCF4 transcription factor 4
TMED2 transmembrane emp24 domain trafficking protein 2
TP63 tumor protein p63
WNT3A wingless-type MMTV integration site family, member 3A