abnormal joint mobility Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability to move joints in a full range of motion and with ease (Mammalian Phenotype Ontology, MP_0008069)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008069
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11 gene mutations causing the abnormal joint mobility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
ADGRG6 adhesion G protein-coupled receptor G6
ANKH ANKH inorganic pyrophosphate transport regulator
COL11A1 collagen, type XI, alpha 1
COL2A1 collagen, type II, alpha 1
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
IL6ST interleukin 6 signal transducer
LPIN1 lipin 1
MEOX2 mesenchyme homeobox 2
NOV nephroblastoma overexpressed
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4