|
3581
|
|
|
Jade family PHD finger 2 |
JADE-2, PHF15 |
|
|
3582
|
|
|
VPS39 subunit of HOPS complex |
TLP, VAM6, hVam6p |
|
|
3583
|
|
|
ALF transcription elongation factor 2 |
FMR2, FMR2P, FRAXE, MRX2, OX19, XLID109 |
Autism, Camptodactyly of fingers, Congenital epicanthus, Dwarfism, Fragile x syndrome, Hand flapping, Macrocephaly, Mental retardation, Obsessive-compulsive disorder, Specific learning disorder, Stereotypy |
|
3584
|
|
|
DnaJ heat shock protein family (Hsp40) member C16 |
ERdj8 |
|
|
3585
|
|
|
Extended synaptotagmin 1 |
FAM62A, MBC2 |
|
|
3586
|
|
|
Spectrin repeat containing nuclear envelope protein 1 |
8B, AMC3, AMCM, ARCA1, C6orf98, CPG2, EDMD4, KASH1, MYNE1, Nesp1, SCAR8, dJ45H2.2 |
Amyotrophy, Arthrogryposis multiplex congenita, Ataxia, Atrioventricular block, Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Colorectal cancer, Colorectal neoplasms, Congenital clubfoot, Congenital muscular dystrophy, Congenital pectus excavatum, Cryptorchidism, Depressed bipolar disorder, Development disorder, Developmental delay, Developmental regression, Distal arthrogryposis, Dysarthria, Elbow flexion contracture, Emery-dreifuss muscular dystrophy, Emery-dreifuss muscular dystrophy, x-linked, Endometriosis, Horizontal nystagmus, Hyperopia, Hypertrophic cardiomyopathy, Ichthyosis, Limb-girdle muscular dystrophy, Lipodystrophy, Marfan syndrome, Mental depression, Mental retardation, Motor delay, Muscular dystrophy, Myogenic arthrogryposis multiplex congenita, Nasopharyngeal carcinoma, Nystagmus, Obesity, Peripheral axonal neuropathy, Ptosis, Schizophrenia, Scoliosis, Spinocerebellar ataxia, Sprengel deformity, Strabismus, Uterine fibroids, Plexiform leiomyoma, Ventricular septal hypertrophy, Vocal cord paralysisView all (39 more) |
|
3587
|
|
|
Structural maintenance of chromosomes flexible hinge domain containing 1 |
BAMS, FSHD2 |
Arrhinia, Arrhinia with choanal atresia and microphthalmia syndrome, Cataract, Choanal atresia, Congenital coloboma of iris, Congenital hypoplasia of penis, Congenital ocular coloboma, Cryptorchidism, Facioscapulohumeral dystrophy, Facioscapulohumeral muscular dystrophy, Gynecomastia, Hearing loss, High palate, Hypogonadism, Hypoplasia of the olfactory bulb, Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome, Microphthalmos, Muscular dystrophy, Penis agenesis, Physiologic amenorrhea, Submucosal cleft palate, Syndromic microphthalmiaView all (7 more) |
|
3588
|
|
|
Dedicator of cytokinesis 9 |
ZIZ1, ZIZIMIN1 |
|
|
3589
|
|
|
Fibronectin 1 |
CIG, ED-B, FINC, FN, FNZ, GFND, GFND2, LETS, MSF, SMDCF |
Alveolitis, Anaplastic carcinoma, Aortic valve insufficiency, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Colorectal cancer, Coronary artery disease, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Diabetes mellitus, Diabetic nephropathy, Distal tubular acidosis, Dwarfism, Endometriosis, Fibronectin glomerulopathy, Giant cell glioblastoma, Glioblastoma, Glomerular hyalinosis, Glomerulopathy with fibronectin deposits, Glomerulosclerosis, Hypertension, Hypoalbuminemia, Ileocolitis, Kidney disease, Left ventricular hypertrophy, Malignant mesothelioma, Marfan syndrome, Micromelia, Miscarriage, Nephrotic syndrome, Pulmonary fibrosis, Renal carcinoma, Renal glomerular disease, Renal insufficiency, Scoliosis, Spondylometaphyseal dysplasia, Strudwick syndrome, Tetralogy of fallotView all (26 more) |
|
3590
|
|
|
KH and NYN domain containing |
KIAA0323 |
|
