|
1281
|
|
|
CD27 molecule |
S152, S152. LPFS2, T14, TNFRSF7, Tp55 |
|
|
1282
|
|
|
CD28 molecule |
IMD123, Tp44 |
Alopecia, Autoimmune diseases, Celiac disease, Ectropion, Eczema, Exfoliative dermatitis, Gangrene, Granulomatous slack skin, Hyperkeratosis, Immunologic deficiency syndromes, Inflammatory bowel disease, Lymphoma, Nail dystrophy, Nervous system diseases, Palmoplantar keratoderma, Poikiloderma, Rheumatoid arthritis, Sezary syndrome, Skin neoplasms, T-cell lymphoma, T-cell lymphoma/leukemia, Ulcerative colitisView all (7 more) |
|
1283
|
|
|
CD80 molecule |
B7, B7-1, B7.1, BB1, CD28LG, CD28LG1, LAB7 |
|
|
1284
|
|
|
CDRT15 pseudogene 1 |
CDRT15P |
|
|
1285
|
|
|
CXXC repeat containing interactor of PDZ3 domain |
HSPC139, RTS3, SSMDF |
Anemia, Brachydactyly, Congenital clubfoot, Developmental delay, Dwarfism, Dyscognitive seizures, Exotropia, Frontal bossing, Microcephaly, Myopia, Nystagmus, Osteopenia, Pituitary dwarfism, Proptosis, Seizure, Short stature with microcephaly and distinctive facies, SyndactylyView all (2 more) |
|
1286
|
|
|
CD86 molecule |
B7-2, B7.2, B70, CD28LG2, LAB72 |
|
|
1287
|
|
|
Cytochrome P450 family 7 subfamily B member 1 |
CBAS3, CP7B, SPG5A |
Adenocarcinoma, Atrophy of the spinal cord, Blood coagulation disorders, Carcinoma, Cataract, Charcot-marie-tooth disease, Cholestasis, Cirrhosis, Congenital bile acid synthesis defect, Congenital hepatic fibrosis, Dysarthria, Dysphagia, Fatty liver, Hearing loss, Immunodeficiency, Intrahepatic cholestasis, Limb amyotrophy, Lipid metabolism, inborn errors, Liver failure, Mental depression, Nystagmus, Optic atrophy, Paraplegia, Polyneuropathy, Prostatic neoplasms, Prostate cancer, Scoliosis, Spastic paraplegia, Hereditary spastic paraplegia, x-linkedView all (14 more) |
|
1288
|
|
|
Chromodomain Y like |
CDYL1 |
|
|
1289
|
|
|
Chromodomain Y-linked 2A |
CDY, CDY2 |
|
|
1290
|
|
|
CD33 molecule |
CD33rSiglec, SIGLEC-3, SIGLEC3, p67 |
|
