|
161
|
|
|
Ankyrin repeat and SOCS box containing 10 |
GLC1F |
|
|
162
|
|
|
Ankyrin repeat, SAM and basic leucine zipper domain containing 1 |
ALP1, ANKL1, C7orf7, CT1.19, GASZ, Orf3 |
|
|
163
|
|
|
Actin binding Rho activating protein |
STARS |
|
|
164
|
|
|
Alcohol dehydrogenase iron containing 1 |
ADH8, HMFT2263, HOT |
|
|
165
|
|
|
Activating transcription factor 2 |
CRE-BP1, CREB-2, CREB2, HB16, TREB7 |
|
|
166
|
|
|
Ankyrin repeat domain 19, pseudogene |
ANKRD19, bA526D8.2 |
|
|
167
|
|
|
Activating transcription factor 6 beta |
ATF6beta, CREB-RP, CREBL1, G13 |
|
|
168
|
|
|
APC membrane recruitment protein 1 |
FAM123B, OSCS, WTX |
Aortic coarctation, Aortic valve sclerosis, Aphasia, Arachnodactyly, Atrial septal defect, Brachycephaly, Camptodactyly of fingers, Cataract, Congenital camptodactyly, Congenital clubfoot, Congenital epicanthus, Congenital malrotation of intestine, Congenital pectus excavatum, Developmental delay, Dwarfism, Dysmorphic features, Dysphasia, Facial paralysis, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Hydrocephalus, Laryngeal web, Macrocephaly, Mental retardation, Micrognathism, Microtia, Multiple congenital anomalies, Neck webbing, Nephroblastoma, Osteopathia striata, Osteopathia striata cranial sclerosis, Osteopetrosis, Partial agenesis of corpus callosum, Patent ductus arteriosus, Pierre-robin syndrome, Posteriorly rotated ear, Scoliosis, Specific learning disorder, Spina bifida occulta, Submucosal cleft palate, Tracheomalacia, Ventricular septal defect, Wilms tumorView all (29 more) |
|
169
|
|
|
Actin related protein T1 |
AIP1, ARIP1, ARPT1, HSD27 |
|
|
170
|
|
|
Adenosine A3 receptor |
A3AR |
|
