|
1671
|
|
|
Solute carrier family 16 member 10 |
MCT10, PRO0813, TAT1 |
|
|
1672
|
|
|
Inositol hexakisphosphate kinase 3 |
IHPK3, INSP6K3 |
|
|
1673
|
|
|
Calcium and integrin binding family member 3 |
KIP3 |
|
|
1674
|
|
|
T cell activation RhoGTPase activating protein |
ARHGAP47, FKSG15, IDDM21, TAGAP1 |
Asthma, Autoimmune diseases, Celiac disease, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Ileocolitis, Immune system diseases, Multiple sclerosis, Palmoplantar pustules, Psoriasis, Rheumatoid arthritis |
|
1675
|
|
|
Adaptor related protein complex 2 subunit mu 1 |
AP50, CLAPM1, MRD60, mu2 |
|
|
1676
|
|
|
Adaptor related protein complex 1 subunit sigma 1 |
AP19, CLAPS1, EKV3, MEDNIK, SIGMA1A |
Cholestasis, Cirrhosis, Developmental delay, Erythrokeratoderma, Hyperkeratosis, Ichthyosis, Intrahepatic cholestasis, Lipoidosis, Liver fibrosis, Mednik syndrome, Mental retardation, Nervous system diseases |
|
1677
|
|
|
Adaptor related protein complex 2 subunit sigma 1 |
AP17, CLAPS2, FBH3, FBHOk, HHC3 |
|
|
1678
|
|
|
Transmembrane channel like 1 |
DFNA36, DFNB11, DFNB7 |
|
|
1679
|
|
|
Relaxin 3 |
H3, RXN3, ZINS4, insl7 |
|
|
1680
|
|
|
Twist family bHLH transcription factor 2 |
AMS, BBRSAY, DERMO1, FFDD3, SETLSS, bHLHa39 |
Ablepharon, Ablepharon macrostomia syndrome, Absent eyebrow, Alopecia, Ambiguous genitalia, Barber say syndrome, Cafe-au-lait spot, Breast aplasia, Congenital absent nipple, Congenital ectodermal dysplasia of face, Congenital epicanthus, Congenital exomphalos, Breast hypoplasia, Congenital hypoplasia of penis, Congenital omphalocele, Corneal erosion, Cryptophthalmos, Developmental delay, Ectodermal dysplasia, Ectropion, Focal facial dermal dysplasia, Hypertrichosis, Hypoplasia of nipple, Hypoplasia of the maxilla, Imperforate anus, Macrostomia, Malocclusion, Microdontia, Microtia, Mouth abnormalities, Multiple congenital anomalies, Myopia, Strabismus, Syndactyly of the toesView all (19 more) |
