|
61
|
|
|
Spondin 2 |
DIL-1, DIL1, M-SPONDIN, MINDIN |
|
|
62
|
|
|
Spondin 1 |
VSGP/F-spondin, f-spondin |
|
|
63
|
|
|
Small nucleolar RNA host gene 14 |
115HG, IC-SNURF-SNRPN, LNCAT, NCRNA00214, U-UBE3A-ATS, UBE3A-AS, UBE3A-AS1, UBE3A-ATS, UBE3AATS |
|
|
64
|
|
|
Solute carrier family 30 member 9 |
BILAPES, C4orf1, GAC63, HUEL, ZNT9 |
Birk-landau-perez syndrome, Choreoathetosis, Developmental regression, Dyskinetic syndrome, Impaired cognition, Mental depression, Nephritis, Oculomotor apraxia, Oculovestibuloauditory syndrome, Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome, Ptosis, Renal insufficiency |
|
65
|
|
|
Solute carrier family 25 member 17 |
PMP34 |
|
|
66
|
|
|
Solute carrier family 9 member A6 |
MRSA, MRXSCH, NDPACX, NHE6 |
Arthrogryposis multiplex congenita, Autism, Bowel incontinence, Camptodactyly of fingers, Cerebellar atrophy, Cerebral cortical atrophy, Christianson syndrome, Congenital anomaly of nose, Congenital pectus excavatum, Developmental delay, Developmental regression, Dysphagia, Dyssomnia, Esotropia, Gastroesophageal reflux disease, Mental retardation, Macrotia, Malocclusion, Microcephaly, Nystagmus, Photosensitive tonic-clonic seizures, Scoliosis, Seizure, Sleep disorders, Stereotyped behavior, StrabismusView all (11 more) |
|
67
|
|
|
SEC23 homolog B, COPII component |
CDA-II, CDAII, CDAN2, CWS7, HEMPAS, hSec23B |
Adenoma sebaceum, Anemia, Autism, Brachydactyly, Breast carcinoma, Cafe-au-lait spot, Cataract, Cholelithiasis, Congenital dyserythropoietic anemia, Congenital pectus excavatum, Conjunctival hamartoma, Cowden syndrome, Developmental delay, Dwarfism, Endometrial carcinoma, Enlarged polycystic ovaries, Follicular thyroid carcinoma, Gynecomastia, Hamartoma, Hamartomatous polyposis, Hashimoto disease, Hemangioma, Hemangioma, cavernous, High palate, Hypogonadotropic hypogonadism with or without anosmia, Ichthyosis with hypotrichosis, Impaired cognition, Intestinal polyposis, Lipoma, Macrocephaly, Macroglossia, Melanocytic nevus, Melanoma, Meningioma, Mental retardation, Myopia, Ductal carcinoma, Palmoplantar keratoderma, Papillary thyroid carcinoma, Papilloma, Polyp of large intestine, Renal carcinoma, Scoliosis, Trichilemmoma, Usher syndromeView all (30 more) |
|
68
|
|
|
SEC23 homolog A, COPII component |
CLSD, hSec23A |
Arthritis, Craniolenticulosutural dysplasia, Cryptorchidism, Defect of skull ossification, Dwarfism, Frontal bossing, High palate, Hypoplasia of teeth, Hypoplasia of the maxilla, Macrocephaly, Macrostomia, Microdontia, Osteoarthrosis deformans, Osteochondrodysplasia, Punctate cataract, Scoliosis, Skeletal dysplasia, Strawberry nevus of skin, Sutural cataractView all (4 more) |
|
69
|
|
|
Synaptotagmin binding cytoplasmic RNA interacting protein |
GRY-RBP, GRYRBP, HNRNPQ, HNRPQ1, NSAP1, PP68, hnRNP-Q |
|
|
70
|
|
|
Serine/threonine kinase 25 |
SOK1, YSK1 |
|
