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2451
|
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|
Long intergenic non-protein coding RNA 964 |
- |
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2452
|
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Establishment of sister chromatid cohesion N-acetyltransferase 2 |
2410004I17Rik, EFO2, EFO2p, JHS, RBS, hEFO2 |
Aortic valve sclerosis, Atrial septal defect, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cataract, Clinodactyly, Talipes equinovalgus, Congenital hypoplasia of radius, Congenital ocular coloboma, Cranial nerve paralysis, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism, Elbow flexion contracture, Flexion contracture of wrist, Frontal encephalocele, Glaucoma, High palate, Hip contracture, Horseshoe kidney, Hydrocephalus, Hypertrophy of clitoris, Hypoplasia of thumb, Hypospadias, Kidney neoplasm, Kidney cancer, Cystic hygroma, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Midface capillary hemangioma, Nystagmus, Patent ductus arteriosus, Phocomelia, Polycystic kidney disease, Posteriorly rotated ear, Proptosis, Radial aplasia, Radioulnar synostosis, Roberts syndrome, Roberts-sc phocomelia syndrome, Syndactyly, Syndactyly of fingers, Tetraphocomelia, Ventricular septal defectView all (33 more) |
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2453
|
|
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Cytochrome P450 family 3 subfamily A member 4 |
CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1, VDDR3 |
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2454
|
|
|
Cilia and flagella associated protein 418 |
BBS21, C8orf37, CORD16, FAP418, MOT25, RP64, smalltalk |
Anetoderma, Bardet-biedl syndrome, Cataract, Cone-rod dystrophy, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Diabetes mellitus, Disorder of eye, Dwarfism, Glaucoma, Hearing loss, Horseshoe kidney, Hyperinsulinism, Hypertension, Hypodontia, Hypogonadism, Keratoconus, Liver fibrosis, Mental retardation, Multicystic renal dysplasia, Myopia, Nephrotic syndrome, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (17 more) |
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2455
|
|
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Vacuolar protein sorting 13 homolog B |
BLTP5B, CHS1, COH1 |
Cubitus valgus, Aphthous ulcer, Arachnodactyly, Attention deficit hyperactivity disorder, Breast cancer, Camptodactyly of fingers, Cerebellar hypoplasia, Chorioretinal dystrophy, Cohen syndrome, Congenital coloboma of iris, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Dwarfism, Dysmorphic features, Hearing loss, Hypoplasia of the maxilla, Isolated somatotropin deficiency, Laryngomalacia, Leukopenia, Macrodontia, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Mitral valve prolapse, Motor delay, Movement disorders, Myopia, Hypotonia, Neutropenia, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Scoliosis, Somatotropin deficiency, Speech disorders, Strabismus, Syndactyly of fingers, Ventricular septal defectView all (27 more) |
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2456
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|
|
Glutamate rich 1 |
HSPC319 |
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2457
|
|
|
Cytochrome P450 family 3 subfamily A member 5 |
CP35, CYPIIIA5, P450PCN3, PCN3 |
|
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2458
|
|
|
Solute carrier family 7 member 13 |
AGT-1, AGT1, XAT2 |
|
|
2459
|
|
|
Transmembrane protein 74 |
NET36 |
|
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2460
|
|
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Cytochrome P450 family 3 subfamily A member 51, pseudogene |
CYP3A5-de13c, CYP3A5-de1b2b, CYP3A5P1, CYP3AP1 |
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