|
761
|
|
|
Mitochondrially encoded cytochrome b |
MTCYB |
Wolff-parkinson-white syndrome, Breast cancer, Central visual impairment, Colorectal cancer, Congestive heart failure, Dementia, Diabetes mellitus, Epileptic encephalopathy, Hemianopsia, Hereditary leber optic atrophy, Histiocytoid cardiomyopathy, Hypertension, Left ventricular hypertrophy, Leigh syndrome, Melas syndrome, Migraine, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Myopathy, Nervous system diseases, Optic atrophy, Ovarian neoplasm, Polyneuropathy, Retinal telangiectasia, Seizure, Sensorineural hearing loss, Ventricular preexcitationView all (12 more) |
|
762
|
|
|
CEA cell adhesion molecule 6 |
CD66c, CEAL, NCA, NCA-50/90 |
|
|
763
|
|
|
CCR4-NOT transcription complex subunit 2 |
CDC36, HSPC131, IDNADFS, NOT2, NOT2H |
|
|
764
|
|
|
CCR4-NOT transcription complex subunit 3 |
IDDSADF, LENG2, NOT3, NOT3H |
|
|
765
|
|
|
CCR4-NOT transcription complex subunit 4 |
CLONE243, NOT4, NOT4H |
|
|
766
|
|
|
Cytochrome c oxidase assembly factor 5 |
6330578E17Rik, C2orf64, CEMCOX3, MC4DN9, Pet191 |
|
|
767
|
|
|
CDGSH iron sulfur domain 2 |
ERIS, Miner1, NAF-1, WFS2, ZCD2 |
Anemia, Cardiomyopathy, Cerebral cortical atrophy, Dementia, Developmental regression, Diabetes insipidus, Diabetes mellitus, Dysarthria, Dysautonomia, Dyssomnia, Gastric ulcer, Glaucoma, Hallucinations, Hearing loss, Kidney disease, Malabsorption syndrome, Mental depression, Mental retardation, Myopathy, Nervous system diseases, Neurogenic urinary bladder, Nystagmus, Optic atrophy, Physiologic amenorrhea, Sleep apnea, Sleep disorders, Testicular hypogonadism, Wolfram syndromeView all (13 more) |
|
768
|
|
|
Cornulin |
C1orf10, DRC1, PDRC1, SEP53 |
|
|
769
|
|
|
Claudin 11 |
HLD22, OSP, OTM |
|
|
770
|
|
|
CD207 molecule |
CLEC4K |
|
