|
171
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 14 |
- |
|
|
172
|
|
|
Ankyrin repeat and SOCS box containing 15 |
- |
|
|
173
|
|
|
Rho GTPase activating protein 42 |
AD031, GRAF3, TMEM133 |
|
|
174
|
|
|
ALG10 alpha-1,2-glucosyltransferase B |
ALG10, KCR1 |
|
|
175
|
|
|
Alpha-2-macroglobulin like 1 |
CPAMD9, OMS, p170 |
Abnormal dermatoglyphic pattern, Brachydactyly, Camptodactyly of fingers, Cardiofaciocutaneous syndrome, Congenital pectus carinatum, Congenital pectus excavatum, Costello syndrome, Cryptorchidism, Dwarfism, Dysarthria, Hearing loss, High palate, Hypogonadotropic hypogonadism, Leopard syndrome, Cystic hygroma, Melanocytic nevus, Micrognathism, Neck webbing, Noonan syndrome, Noonan-like syndrome with loose anagen hair, Nystagmus, Otitis media, Proptosis, Ptosis, Radioulnar synostosis, Scoliosis, StrabismusView all (12 more) |
|
176
|
|
|
Armadillo like helical domain containing 4 |
C14orf37, UT2, c14_5376 |
|
|
177
|
|
|
Abhydrolase domain containing 12B |
BEM46L3, C14orf29, c14_5314 |
|
|
178
|
|
|
Adrenoceptor alpha 1D |
ADRA1, ADRA1A, ADRA1R, ALPHA1, DAR, dJ779E11.2 |
|
|
179
|
|
|
Adrenoceptor alpha 1B |
ADRA1, ALPHA1BAR |
|
|
180
|
|
|
AQP4 antisense RNA 1 |
C18orf16, CHST9-AS1 |
|
