|
161
|
|
|
Four and a half LIM domains 2 |
AAG11, DRAL, FHL-2, SLIM-3, SLIM3 |
Breast cancer, Mammary neoplasms, Breast carcinoma, Cardiomyopathy, Dilated cardiomyopathy, Hearing loss, Leukemia, Lipoatrophy, Lipodystrophy, Marfan syndrome, Myeloid leukemia, Myopathy, Palmoplantar keratoderma |
|
162
|
|
|
Four and a half LIM domains 3 |
SLIM2 |
|
|
163
|
|
|
FKBP prolyl isomerase 1A |
FKBP-12, FKBP-1A, FKBP1, FKBP12, PKC12, PKCI2, PPIASE |
|
|
164
|
|
|
FERM and PDZ domain containing 1 |
FRMD2 |
|
|
165
|
|
|
FKBP prolyl isomerase 2 |
FKBP-13, FKBP13, PPIase |
|
|
166
|
|
|
Fibronectin type III domain containing 3A |
FNDC3, HUGO, bA203I16.1, bA203I16.5 |
|
|
167
|
|
|
FAST kinase domains 2 |
COXPD44, KIAA0971 |
Anemia, Cytochrome-c oxidase deficiency, Developmental delay, Encephalomyopathy, Fanconi syndrome, Hearing loss, High palate, Hypertrophic cardiomyopathy, Leukoencephalopathy, Mental retardation, Mitochondrial diseases, Motor delay, Optic atrophy, Phosphate diabetes, Ptosis, Renal tubular disorder, Retinitis pigmentosaView all (2 more) |
|
168
|
|
|
FKBP prolyl isomerase 4 |
FKBP51, FKBP52, FKBP59, HBI, Hsp56, PPIase, p52 |
|
|
169
|
|
|
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 |
|
170
|
|
|
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) |
