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3281
|
|
|
Netrin G1 |
Lmnt1, NetG1, NetrinG1 |
Bipolar disorder, Camptodactyly of fingers, Cerebral cortical atrophy, Colorectal cancer, Colorectal neoplasms, Developmental regression, Gastroesophageal reflux disease, Macrostomia, Manic disorder, Mental retardation, Microcephaly, Movement disorders, Nephrolithiasis, Rett syndrome, Schizophrenia, Syndromic mental retardationView all (1 more) |
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3282
|
|
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Chondroitin sulfate synthase 1 |
CHSY, CSS1, ChSy-1, TPBS |
Brachydactyly, Camptodactyly of fingers, Carpal synostosis, Clinodactyly, Developmental delay, Dwarfism, Hypodontia, Hypoplasia of the maxilla, Mental retardation, Microdontia, Micrognathism, Microstomia, Non-obstructive azoospermia, Oligodontia, Optic atrophy, Plagiocephaly, Sensorineural hearing loss, Specific learning disorder, Syndactyly, Syndactyly of fingers, Synophrys, Tarsal coalition, Temtamy preaxial brachydactyly syndromeView all (8 more) |
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3283
|
|
|
Ciliogenesis associated kinase 1 |
ECO, EJM10, ICK, LCK2, MRK, hICK |
Ambiguous genitalia, Brachydactyly, Cryptorchidism, Endocrine-cerebroosteodysplasia, Febrile seizures, Holoprosencephaly, Hydrocephalus, Hypospadias, Mesomelia, Micrognathism, Micromelia, Mouth abnormalities, Myoclonic epilepsy, Myoclonic seizures, Penis agenesis, Photosensitive tonic-clonic seizures, Polydactyly, Radial polydactyly, Renal carcinoma, Rhizomelia, Short rib-polydactyly syndrome, Status epilepticus, SyndactylyView all (8 more) |
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3284
|
|
|
FKBP prolyl isomerase 2 |
FKBP-13, FKBP13, PPIase |
|
|
3285
|
|
|
NLR family pyrin domain containing 1 |
AIADK, CARD7, CIDED, CLR17.1, DEFCAP, DEFCAP-L/S, JRRP, MSPC, NAC, NALP1, PP1044, SLEV1, VAMAS1 |
Autoimmune hemolytic anemia, Autoinflammation with arthritis and dyskeratosis, Autoinflammatory disease, Carcinoma, Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome, Corneal neovascularization, Ectodermal dysplasia, Hypereosinophilia, Hyperkeratosis, Keratoconjunctivitis sicca, Limbal stem cell deficiency, Macular amyloidosis, Palmoplantar carcinoma, Palmoplantar keratoderma, Parakeratosis, Phrynoderma, Polyarthritis, Punctate keratitis, Thyroiditis, Uveitis, Vitiligo, Vitiligo-associated systemic lupus erythematosusView all (7 more) |
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3286
|
|
|
Fibronectin type III domain containing 3A |
FNDC3, HUGO, bA203I16.1, bA203I16.5 |
|
|
3287
|
|
|
R3H domain containing 2 |
CAG6, PR01365 |
|
|
3288
|
|
|
Connector enhancer of kinase suppressor of Ras 2 |
CNK2, KSR2, MAGUIN, MRXSHG |
Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Colorectal cancer, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Facial paralysis, Gastroesophageal reflux disease, Neurosensory hearing impairment, Hypodontia, Mental retardation, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Microcephaly, Non-specifi epileptic encephalopathy, Non-syndromic intellectual disability, x-linked, Nystagmus, Obesity, Optic atrophy, Ptosis, Seizure, Status epilepticus, Syndactyly of the toesView all (13 more) |
|
3289
|
|
|
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) |
|
3290
|
|
|
Neuroligin 1 |
NL1, NLG1 |
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