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1761
|
|
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C-C motif chemokine receptor 1 |
CD191, CKR-1, CKR1, CMKBR1, HM145, MIP1aR, SCYAR1 |
Acne, Anorexia, Aortic valve insufficiency, Aphthous ulcer, Arthritis, Behcet syndrome, Cataract, Cranial nerve paralysis, Dermatitis, Developmental regression, Encephalitis, Endocarditis, Gangrene, Keratoconjunctivitis sicca, Liver carcinoma, Malabsorption syndrome, Migraine, Myocardial infarction, Myositis, Oral ulcer, Pancreatitis, Pericarditis, Pleural effusion, Pleuritis, Renal glomerular disease, Renal insufficiency, Retinal diseases, Retrobulbar neuritis, VasculitisView all (14 more) |
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1762
|
|
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Tetratricopeptide repeat domain 8 |
BBS8, RP51 |
Bardet-biedl syndrome, Brachycephaly, Cataract, Ciliopathies, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Diabetes mellitus, Disorder of eye, Dwarfism, Foot polydactyly, Glaucoma, Hearing loss, Hyperinsulinism, Hypertension, Hypogonadism, Hypospadias, Impaired cognition, Keratoconus, Liver fibrosis, Age-related macular degeneration, Mental retardation, Multicystic renal dysplasia, Myopia, Nephrotic syndrome, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Polydactyly, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (21 more) |
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1763
|
|
|
Tandem C2 domains, nuclear |
C14orf47, C2CD1, MTAC2D1, TAC2N, Tac2-N |
|
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1764
|
|
|
Solute carrier family 24 member 4 |
AI2A5, NCKX4, SHEP6, SLC24A2 |
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1765
|
|
|
Kelch like family member 33 |
- |
|
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1766
|
|
|
C-C motif chemokine receptor 3 |
C C CKR3, CC-CKR-3, CD193, CKR 3, CKR3, CMKBR3 |
Alveolitis, Arthritis, Asthma, Autoimmune diseases, Behcet syndrome, Celiac disease, Dermatitis, Eczema, Grand mal status epilepticus, Immune system diseases, Multiple sclerosis, Nonconvulsive status epilepticus, Oligoarticular arthritis, Pauciarticular chronic arthritis, Petit mal status, Pulmonary fibrosis, Rheumatoid arthritis, Seronegative polyarthritis, Status epilepticus, Still diseaseView all (5 more) |
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1767
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Mitochondrial methionyl-tRNA formyltransferase |
COXPD15, FMT1, MC1DN27 |
Anemia, Attention deficit hyperactivity disorder, Cerebellar ataxia, Combined oxidative phosphorylation deficiency, Developmental delay, Dysarthria, Hypertrichosis, Hypertrophic cardiomyopathy, Impaired cognition, Mental retardation, Leigh syndrome, Leigh syndrome with leukodystrophy, Leukodystrophy, Mitochondrial complex deficiency, Mitochondrial encephalomyopathy, Mood swings, Nervous system diseases, Neurogenic urinary bladder, Nystagmus, Optic atrophy, Ptosis, Retinitis pigmentosa, Strabismus, Ventricular septal defectView all (9 more) |
|
1768
|
|
|
SLC51 subunit beta |
OSTB, OSTBETA, PBAM2, SLC51A1BP |
|
|
1769
|
|
|
C-C motif chemokine receptor 4 |
CC-CKR-4, CD194, CKR4, CMKBR4, ChemR13, HGCN:14099, K5-5 |
|
|
1770
|
|
|
C-C motif chemokine receptor 5 |
CC-CKR-5, CCCKR5, CCR-5, CD195, CKR-5, CKR5, CMKBR5, IDDM22 |
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