|
3301
|
|
|
FKBP prolyl isomerase 5 |
AIG6, FKBP51, FKBP54, P54, PPIase, Ptg-10 |
Bipolar disorder, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Coronary artery disease, Endometrioma, Endometriosis, Involutional depression, Involutional paraphrenia, Mental depression, Mood disorder, Nonorganic psychosis, Psychosis, Rheumatoid arthritis |
|
3302
|
|
|
Zinc finger protein 365 |
Su48, UAN, ZNF365D |
Amnesia, Ankylosing spondylitis, Asthma, Basal cell neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Cataplexy, Cholangitis, Crohn disease, Dermatitis, Eczema, Hallucinations, Marfan syndrome, Narcolepsy, Narcolepsy-cataplexy syndrome, Obesity, Psoriasis, Schizophrenia, Ulcerative colitisView all (6 more) |
|
3303
|
|
|
Rabphilin 3A |
- |
|
|
3304
|
|
|
Centrosomal protein 164 |
NPHP15 |
Cataract, Ciliopathies, Congenital hepatic fibrosis, Developmental delay, Dwarfism, Hypertension, Kidney disease, Nephronophthisis, Polydactyly, Premature menopause, Renal dysplasia and retinal aplasia, Retinal dystrophy, Senior-loken syndrome |
|
3305
|
|
|
DENN domain containing 3 |
- |
|
|
3306
|
|
|
Rho guanine nucleotide exchange factor 15 |
ARGEF15, E5, Ephexin5, Vsm-RhoGEF |
|
|
3307
|
|
|
Aldolase, fructose-bisphosphate B |
ALDB, ALDO2 |
Autoimmune hepatitis, Blood coagulation disorders, Cataract, Cirrhosis, Fatty liver, Gastric cancer, Hereditary fructose intolerance, Hereditary fructosuria, Hyperbilirubinemia, Hypermagnesemia, Hyperuricemia, Hypoglycemia, Kidney disease, Liver failure, Malnutrition, Mental retardation, Phosphate diabetes, Reactive hypoglycemia, Renal tubular acidosis, Stomach neoplasmsView all (5 more) |
|
3308
|
|
|
Forkhead box G1 |
BF1, BF2, FHKL3, FKH2, FKHL1, FKHL2, FKHL3, FKHL4, FOXG1A, FOXG1B, FOXG1C, HBF-1, HBF-2, HBF-3, HBF-G2, HBF2, HFK1, HFK2, HFK3, KHL2, QIN |
14q11.2 microduplication syndrome, 14q12 microdeletion syndrome, Acrocallosal syndrome, Agenesis of corpus callosum, Apraxia, Autism, Blepharophimosis, Camptodactyly of fingers, Cerebral cortical atrophy, Clonic seizures, Congenital clubfoot, Congenital epicanthus, Congenital microcephaly, Congenital pectus excavatum, Congenital phimosis, Developmental delay, Developmental regression, Dyskinetic syndrome, Dysmorphic features, Epilepsy, Esotropia, Foxg1 syndrome, Gastroesophageal reflux disease, Hypoplasia of corpus callosum, Hypotonic seizures, Mental retardation, Jacksonian seizure, Macroglossia, Macrostomia, Malocclusion, Microcephaly, Microlissencephaly, Motor delay, Movement disorders, Multiple congenital anomalies, Hypotonia, Nephrolithiasis, Nervous system disorder, Neurodevelopmental disorders, Nystagmus, Oculomotor apraxia, Pachygyria, Partial or complete agenesis of corpus callosum, Rett syndrome, Scoliosis, Seizure, Stereotyped behavior, StrabismusView all (33 more) |
|
3309
|
|
|
Caspase recruitment domain family member 8 |
CARDINAL, DACAR, DAKAR, NDPP, NDPP1, TUCAN |
|
|
3310
|
|
|
Arylsulfatase G |
USH4 |
Anxiety disorder, Astigmatism, Cataract, Hallucinations, Hearing loss, Hemianopsia, Mental depression, Musician`s dystonia, Neuronal ceroid lipofuscinosis, Nyctalopia, Schizophrenia, Usher syndrome |
