|
621
|
|
|
Autophagy related 2B |
BLTP4B, C14orf103 |
|
|
622
|
|
|
Anoctamin 1 |
DOG1, INDMS, MYMY7, ORAOV2, TAOS2, TMEM16A |
|
|
623
|
|
|
Angiogenic factor with G-patch and FHA domains 1 |
GPATC7, GPATCH7, HSU84971, HUS84971, VG5Q |
Anemia, Anomalous pulmonary artery, Atrial septal defect, Congestive heart failure, Hemangioma, Hydrops fetalis, Klippel-trenaunay-weber syndrome, Macrocephaly, Mental retardation, Microcephaly, Patent ductus arteriosus, Thrombophilia, Venous insufficiency |
|
624
|
|
|
Anoctamin 10 |
SCAR10, TMEM16K |
Spinocerebellar ataxia, Cataract, Cerebellar ataxia, Cerebellar atrophy, Dysarthria, Gastroesophageal reflux disease, Horizontal nystagmus, Age-related macular degeneration, Mental retardation, Non-hodgkin`s lymphoma of central nervous system, Nystagmus, Ptosis, Seizure, Triglyceride storage disease with ichthyosis |
|
625
|
|
|
Rho guanine nucleotide exchange factor 10 like |
GrinchGEF |
|
|
626
|
|
|
Adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2 |
DIP13B |
|
|
627
|
|
|
Arginine vasopressin receptor 1A |
AVPR V1a, AVPR1, V1aR |
|
|
628
|
|
|
ATPase family AAA domain containing 3A |
HAYOS, PHRINL |
Cardiomyopathy, Cataract, Cerebellar atrophy, Cerebellar hypoplasia, Congenital pectus carinatum, Cryptorchidism, Developmental delay, Distal amyotrophy, Dyssomnia, Esotropia, Frontal bossing, Harel-yoon syndrome, Hypertrophic cardiomyopathy, Hypoplasia of the optic nerve, Malocclusion, Mental retardation, Micrognathism, Myopia, Nystagmus, Ocular anomalies-axonal neuropathy-developmental delay syndrome, Optic atrophy, Peripheral axonal neuropathy, Peripheral neuropathy, Prostatic neoplasms, Prostate cancer, Scoliosis, Sleep disorders, Spinal muscular atrophyView all (13 more) |
|
629
|
|
|
ASXL transcriptional regulator 2 |
ASXH2, SHAPNS |
Allergic rhinitis, Atrial septal defect, Autism, Urinary bladder cancer, Bladder neoplasm, Congenital epicanthus, Developmental delay, Fatty liver, Febrile seizures, Glabellar hemangioma, High palate, Hyperinsulinism, Leukemia, Macrocephaly, Mental retardation, Microtia, Muscular ventricular septal defect, Myeloid leukemia, Hypoglycemia, Nevus, Phakomatosis pigmentovascularis, Posteriorly rotated ear, Proptosis, Ptosis, Scoliosis, Shashi-pena syndrome, Sleep apnea, Strawberry nevus of skinView all (13 more) |
|
630
|
|
|
Acireductone dioxygenase 1 |
APL1, ARD, ARD', Fe-ARD, HMFT1638, MTCBP1, Ni-ARD, SIPL, mtnD |
|
