abnormal tendon morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the structure or form of the tendons, also often called sinews. (Human Phenotype Ontology, HP_0100261)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005503
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Genes

24 gene mutations causing the abnormal tendon morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANKH ANKH inorganic pyrophosphate transport regulator
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ATP7A ATPase, Cu++ transporting, alpha polypeptide
BGN biglycan
COL14A1 collagen, type XIV, alpha 1
COL1A2 collagen, type I, alpha 2
COL6A3 collagen, type VI, alpha 3
COMP cartilage oligomeric matrix protein
DCN decorin
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FBN1 fibrillin 1
FMOD fibromodulin
GATA4 GATA binding protein 4
KIF7 kinesin family member 7
LUM lumican
MKX mohawk homeobox
PAX9 paired box 9
PCOLCE procollagen C-endopeptidase enhancer
PHEX phosphate regulating endopeptidase homolog, X-linked
PTCH1 patched 1
SCX scleraxis basic helix-loop-helix transcription factor
SLIT3 slit homolog 3 (Drosophila)
THBS2 thrombospondin 2
TNMD tenomodulin