|
871
|
|
|
MER proto-oncogene, tyrosine kinase |
MER, RP38, Tyro12, c-Eyk, c-mer |
Anaplastic carcinoma, Anetoderma, Carcinoma, Carcinoma of the head and neck, Cataract, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Glomerulonephritis, Hearing loss, Hereditary paraganglioma-pheochromocytoma syndromes, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Leukemia, Liver cirrhosis, Mental retardation, Multiple sclerosis, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Peripheral retinal atrophy, Pulmonary thromboembolism, Renal carcinoma, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophyView all (15 more) |
|
872
|
|
|
C-type lectin domain containing 10A |
CD301, CLECSF13, CLECSF14, DC-ASGPR, HML, HML2, MGL |
|
|
873
|
|
|
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 |
|
874
|
|
|
Progesterone immunomodulatory binding factor 1 |
C13orf24, CEP90, JBTS33, PIBF |
Cerebellar vermis agenesis, Congenital cerebral hernia, Congenital coloboma of iris, Developmental delay, Hirschsprung disease, Hydrocephalus, Joubert syndrome, Mental retardation, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Oral cleft, Polydactyly of toes, Polymicrogyria, Ptosis, Scoliosis, Situs inversus, StrabismusView all (3 more) |
|
875
|
|
|
Component of oligomeric golgi complex 5 |
CDG2I, GOLTC1, GTC90 |
Arthritis, Atrial fibrillation, Autism, Brainstem atrophy, Central visual impairment, Cerebellar atrophy, Clinodactyly, Congenital disorder of glycosylation, Coronary artery disease, Cryptorchidism, Dwarfism, Hearing loss, High palate, Mental retardation, Microcephaly, Motor delay, Neurogenic urinary bladder, Paroxysmal atrial fibrillation, Penis agenesis, Posteriorly rotated ear, StrabismusView all (6 more) |
|
876
|
|
|
Zinc finger HIT-type containing 1 |
CG1I, ZNFN4A1, p18(Hamlet) |
|
|
877
|
|
|
Follistatin |
FS |
Breast cancer, Mammary neoplasms, Breast carcinoma, Gastric cancer, Liver neoplasms, Liver cancer, Liver carcinoma, Liver failure, Marfan syndrome, Miscarriage, Stomach neoplasms |
|
878
|
|
|
Zinc finger and BTB domain containing 18 |
C1DELq42q44, C1DELq43q44, C2H2-171, DEL1Q42Q44, DEL1Q43Q44, MRD22, RP58, TAZ-1, ZNF238 |
Agenesis of corpus callosum, Congenital epicanthus, Developmental delay, Distal monosomy 1q, Dwarfism, Dysmorphic features, Mental retardation, Microcephaly, Micrognathism, Movement disorders, Multiple congenital anomalies |
|
879
|
|
|
Tripartite motif containing 38 |
RNF15, RORET |
|
|
880
|
|
|
ATP synthase peripheral stalk subunit d |
APT5H, ATP5H, ATPQ |
|
