1281
|
|
|
Component of oligomeric golgi complex 7 |
CDG2E |
|
1282
|
|
|
Component of oligomeric golgi complex 8 |
CDG2H, DOR1 |
|
1283
|
|
|
Collagen type X alpha 1 chain |
- |
|
1284
|
|
|
Collagen type XI alpha 1 chain |
CO11A1, COLL6, DFNA37, STL2 |
Alzheimer disease, Angle closure glaucoma, Attention deficit hyperactivity disorder, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Stickler syndrome, Carpal tunnel syndrome, Congenital cartilage disorder, Connective tissue disease, Craniofacial abnormalities, Deafness, Desbuquois syndrome, Peritoneal disease, Glaucoma, Hearing impairment, Hearing loss, Intervertebral disc disease, Intervertebral disc displacement, Lung cancer, Major depressive disorder, Marshall syndrome, Meniere disease, Myopia, Neurodevelopmental disorder, Open angle glaucoma, Osteoarthritis, Osteochondrodysplasias, Osteogenesis imperfecta, Ovarian cysts, Primary angle closure glaucoma, Retinitis pigmentosa, Scoliosis, Juvenile idiopathic arthritis, Hypertension, Diabetes mellitus type 2, UranostaphyloschisisView all (22 more) |
1285
|
|
|
Collagen type XI alpha 2 chain |
DFNA13, DFNB53, FBCG2, HKE5, OSMEDA, OSMEDB, PARP, STL3 |
Asthma, Isolated sensorineural deafness, Nonsyndromic hearing loss, Otospondylomegaepiphyseal dysplasia, Carpal tunnel syndrome, Cartilage disease, Celiac disease, Interstitial cystitis, Cleft palate, Conductive hearing loss, Congenital cartilage disorder, Congenital ear anomaly, Congenital heart defects, Connective tissue disease, Craniofacial abnormalities, Deafness, Desbuquois syndrome, Down syndrome, Hearing impairment, Hearing loss, Hereditary hearing loss, Hypothyroidism, Inflammatory bowel disease, Intellectual developmental disorder, Congenital anomaly of limb, Lung cancer, Marshall syndrome, Multiple sclerosis, Osteoarthritis, Osteochondrodysplasias, Peptic ulcer disease, Psoriasis, Rheumatoid arthritis, Squamous cell carcinoma, Stickler syndrome, Diabetes mellitus type 1View all (21 more) |
1286
|
|
|
Collagen type XII alpha 1 chain |
BA209D8.1, BTHLM2, COL12A1L, DJ234P15.1, EDSMYP, UCMD2 |
Alzheimer disease, Asthma, Bethlem myopathy, Cataract, Central nervous system cancer, Color vision deficiency, Dementia, Ehlers-danlos syndrome, Endometriosis, Glioblastoma, Glioma, Global developmental delay, Hereditary motor and sensory neuropathies, Keratoconus, Melanoma, Mesothelioma, Neurodevelopmental disorder, Orofacial cleft, Hypertension, Ullrich congenital muscular dystrophyView all (5 more) |
1287
|
|
|
Collagen type XIII alpha 1 chain |
CMS19, COLXIIIA1 |
Liver cirrhosis, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Endometriosis, Migraine, Myasthenic syndrome, Nonalcoholic fatty liver disease, Parkinson disease, Postsynaptic congenital myasthenic syndrome, Presynaptic congenital myasthenic syndrome, Scoliosis, Sialolithiasis, Ulcerative colitis |
1288
|
|
|
Collagen type XIV alpha 1 chain |
UND |
|
1289
|
|
|
Collagen type XV alpha 1 chain |
- |
|
1290
|
|
|
Collagen type XVI alpha 1 chain |
447AA, FP1572 |
|
