3271
|
|
|
Cysteine rich transmembrane module containing 1 |
C5orf32, ORF1-FL49 |
|
3272
|
|
|
Mitochondrially encoded cytochrome b |
MTCYB |
Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss |
3273
|
|
|
- |
- |
Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss |
3274
|
|
|
- |
- |
Developmental delay, Epilepsy, Hearing impairment, Intellectual developmental disorder dysmorphic cerebellar, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Obesity, Leber hereditary optic neuropathy, Hearing loss |
3275
|
|
|
Cytohesin 1 |
B2-1, CYTOHESIN-1, D17S811E, PSCD1, SEC7 |
|
3276
|
|
|
Cytohesin 2 |
ARNO, CTS18, CTS18.1, PSCD2, PSCD2L, SEC7L, Sec7p-L, Sec7p-like, cytohesin-2 |
|
3277
|
|
|
Cytohesin 3 |
ARNO3, GRP1, PSCD3, cytohesin-3 |
|
3278
|
|
|
Cytohesin 4 |
CYT4, DJ63G5.1, PSCD4, cytohesin-4 |
|
3279
|
|
|
Cytohesin 1 interacting protein |
B3-1, CASP, CYBR, CYTHIP, HE, PSCDBP |
|
3280
|
|
|
Cytokine like 1 |
C17, C4orf4 |
Ankylosing spondylitis, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Common variable immunodeficiency, Crohn disease, Hypertension, Juvenile idiopathic arthritis, Psoriasis, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis |