901
|
|
|
ADAMTS like 2 |
ADAMTSL-2, GPHYSD1 |
Acromicric dysplasia, Aortic valve sclerosis, Cardiac valvular disease, Chondrodystrophic myotonia, Congenital anomaly of the hand, Congenital pectus excavatum, Congestive heart failure, Developmental delay, Dwarfism, Dyschondroplasias, Flexion contracture of wrist, Geleophysic dysplasia, Inborn errors of metabolism, Macrostomia, Melnick-needles syndrome, Mitral valve stenosis, Multiple epiphyseal dysplasia, Osteochondrodysplasia, Osteopenia, Schwartz-jampel syndrome, Spondyloenchondrodysplasia, Spondyloepiphyseal dysplasia, Tracheal stenosis, Tricuspid valve stenosis, Van buchem diseaseView all (10 more) |
902
|
|
|
Rho GTPase activating protein 32 |
GC-GAP, GRIT, PX-RICS, RICS, p200RhoGAP, p250GAP |
|
903
|
|
|
ArfGAP with coiled-coil, ankyrin repeat and PH domains 1 |
CENTB1 |
|
904
|
|
|
Adhesion G protein-coupled receptor E5 |
CD97, TM7LN1 |
|
905
|
|
|
Acylphosphatase 2 |
ACYM, ACYP |
|
906
|
|
|
Rho GTPase activating protein 11A |
GAP (1-12) |
|
907
|
|
|
Rho guanine nucleotide exchange factor 11 |
GTRAP48, PDZ-RHOGEF |
|
908
|
|
|
Apoptosis resistant E3 ubiquitin protein ligase 1 |
FIEL1, KIAA0317 |
|
909
|
|
|
Adaptor related protein complex 5 subunit zeta 1 |
KIAA0415, SPG48, zeta |
|
910
|
|
|
ATPase secretory pathway Ca2+ transporting 2 |
SPCA2 |
|