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1541
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Cytochrome P450 family 2 subfamily U member 1 |
P450TEC, SPG49, SPG56 |
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1542
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Cholinergic receptor nicotinic alpha 4 subunit |
BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 |
Acth deficiency, Attention deficit hyperactivity disorder, Autism, Clonic seizures, Development disorder, Epilepsy, Hypotonic seizures, Jacksonian seizure, Mental depression, Minimal brain dysfunction, Nervous system disorder, Nocturnal epilepsy, Schizophrenia, Seizure, Short sleeper syndromes, Sleep disorders, Sleep wake disordersView all (2 more) |
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1543
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Phosphoinositide-3-kinase interacting protein 1 |
HGFL, TrIP, hHGFL(S) |
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1544
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Cholinergic receptor nicotinic alpha 5 subunit |
LNCR2 |
Anxiety disorder, Chronic obstructive pulmonary disease, Clonic seizures, Development disorder, Hypotonic seizures, Jacksonian seizure, Lung carcinoma, Lung neoplasms, Lung adenocarcinoma, Lung cancer, Schizophrenia, Seizure |
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1545
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Family with sequence similarity 83 member F |
- |
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1546
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Zinc finger protein 257 |
BMZF-4, BMZF4 |
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1547
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Deltex E3 ubiquitin ligase 2 |
RNF58 |
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1548
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Cholinergic receptor nicotinic alpha 7 subunit |
CHRNA7-2, NACHRA7, nAChR7 |
15q13.3 microdeletion syndrome, Alzheimer disease, Attention deficit hyperactivity disorder, Auditory processing disorder, Autism, Bipolar disorder, Camptodactyly of fingers, Clonic seizures, Congenital epicanthus, Congenital exomphalos, Congenital omphalocele, Developmental delay, Dwarfism, Epilepsy, Epilepsy with tonic-clonic seizures, Frontal bossing, Hypotonic seizures, Jacksonian seizure, Leukemia, Lung neoplasms, Lung cancer, Macrocephaly, Macrotia, Major affective disorder, Melanocytic nevus, Memory disorders, Age-related memory disorders, Mental retardation, Microcephaly, Nonconvulsive seizure disorder, Schizophrenia, Seizure, Senile dementia, Spina bifida cystica, Spina bifida, StrabismusView all (21 more) |
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1549
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Adenylate cyclase 8 |
AC8, ADCY3, HBAC1 |
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1550
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Cholinergic receptor nicotinic beta 1 subunit |
ACHRB, CHRNB, CMS1D, CMS2A, CMS2C, SCCMS |
Developmental delay, Facial paralysis, High palate, Hypotonia, Myasthenic syndrome, Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency, Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency, Myopathy, Ptosis, Respiratory failure |