CYCS - cytochrome c, somatic Gene
Also Known as CYC; HCS; THC4
Species: Homo sapiens
About CYCS
This gene has 4 transcripts (splice variants), 135 orthologues and is associated with 2 phenotypes. Broad expression in heart (RPKM 66.9), colon (RPKM 54.4) and 24 other tissues.
Summary
This gene encodes a small heme protein that functions as a central component of the electron transport chain in mitochondria. The encoded protein associates with the inner membrane of the mitochondrion where it accepts electrons from cytochrome b and transfers them to the cytochrome oxidase complex. This protein is also involved in initiation of Apoptosis. Mutations in this gene are associated with autosomal dominant nonsyndromic thrombocytopenia. Numerous processed pseudogenes of this gene are found throughout the human genome.[provided by RefSeq, Jul 2010]
CYCS Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_018947.6 | NP_061820.1 | cytochrome c |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
9267021 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| part of apoptosome |
IPI
IPI: Inferred from physical interaction
|
10206961 | GOA |
| located in cytosol |
IDA
IDA: Inferred from direct assay
|
12107093 | GOA |
| located in cytosol |
IMP
IMP: Inferred from mutant phenotype
|
8689682 | GOA |
| located in mitochondrial intermembrane space |
IDA
IDA: Inferred from direct assay
|
19393246 | GOA |
| located in mitochondrion |
IDA
IDA: Inferred from direct assay
|
12107093 | GOA |
CYCS Protein Structure
Cytochrom_C: Cytochrome c (4 - 101)
- 0
- 100
- 105 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
cytochrome c |
|
CYCS Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
CYCS | P99999 | KRT40 | Homo sapiens | Q6A162 | 25910212 | |
|
Intra
|
CYCS | P99999 | KRT40 | Homo sapiens | Q6A162 | 25416956 | |
|
Intra
|
CYCS | P99999 | KRT40 | Homo sapiens | Q6A162 | 25416956 | |
|
Intra
|
CYCS | P99999 | KRT40 | Homo sapiens | Q6A162 | 25910212 | |
|
Intra
|
CYCS | P99999 | KRT40 | Homo sapiens | Q6A162 | 25910212 | |
|
Intra
|
CYCS | P99999 | MEOX2 | Homo sapiens | Q6FHY5 | 32296183 | |
|
Intra
|
CYCS | P99999 | MEOX2 | Homo sapiens | Q6FHY5 | 32296183 | |
|
Intra
|
CYCS | P99999 | MEOX2 | Homo sapiens | Q6FHY5 | 32296183 | |
|
Intra
|
CYCS | P99999 | SYMPK | Homo sapiens | Q92797-2 | 32814053 | |
|
Intra
|
CYCS | P99999 | SYMPK | Homo sapiens | Q92797-2 | 32814053 | |
|
Intra
|
CYCS | P99999 | SYMPK | Homo sapiens | Q92797-2 | 32814053 | |
|
Intra
|
CYCS | P99999 | LONRF2 | Homo sapiens | Q1L5Z9 | 32814053 | |
|
Intra
|
CYCS | P99999 | LONRF2 | Homo sapiens | Q1L5Z9 | 32814053 | |
|
Intra
|
CYCS | P99999 | LONRF2 | Homo sapiens | Q1L5Z9 | 32814053 | |
|
Intra
|
CYCS | P99999 | MLST8 | Homo sapiens | A0A0A0MR05 | 32814053 | |
|
Intra
|
CYCS | P99999 | MLST8 | Homo sapiens | A0A0A0MR05 | 32814053 | |
|
Intra
|
CYCS | P99999 | MLST8 | Homo sapiens | A0A0A0MR05 | 32814053 | |
|
Intra
|
CYCS | P99999 | APAF1 | Homo sapiens | O14727 | 9267021 | |
|
Intra
|
CYCS | P99999 | APAF1 | Homo sapiens | O14727 | 10206961 | |
|
Intra
|
CYCS | P99999 | FYN | Homo sapiens | P06241 | 32814053 | |
|
Intra
|
CYCS | P99999 | FYN | Homo sapiens | P06241 | 32814053 | |
|
Intra
|
CYCS | P99999 | FYN | Homo sapiens | P06241 | 32814053 | |
|
Intra
|
CYCS | P99999 | SEMA4G | Homo sapiens | Q9NTN9-3 | 32814053 | |
|
Intra
|
CYCS | P99999 | SEMA4G | Homo sapiens | Q9NTN9-3 | 32814053 | |
|
Intra
|
CYCS | P99999 | SEMA4G | Homo sapiens | Q9NTN9-3 | 32814053 | |
|
Cross
|
CYCS | P99999 | CYC1-2 | Arabidopsis thaliana | Q9FKS5 | 25595453 |
Recombinant CYCS Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P70053 | Cytochrome c/CYCS Protein, Human (His) | P99999 (G2-E105) | ≥ 95%, as determined by reducing SDS-PAGE. |
CYCS Antibodies
| Cat. No. | Product Name | Application | Reactivity |
|---|---|---|---|
| HY-P80102 | Cytochrome C Antibody (YA479) | WB, ICC/IF, IHC-P, IP | Human, Mouse, Rat |
| HY-P84448 | Cytochrome C Antibody (YA4145) | WB, IHC-P, FC, ELISA | Human, Mouse |
| HY-P84448A | Cytochrome C Antibody (YA4145)(PBS only) | WB, IHC-P, FC, ELISA | Human, Mouse |
| HY-P85730 | Cytochrome C Antibody (YA5422) | WB, ICC/IF, IHC-P | Human, Mouse, Rat, Chicken |
| HY-P86496 | Cytochrome C Antibody (YA6188) | WB, IHC-P, ICC/IF, IP, ELISA | Human, Mouse, Rat |
| HY-P86729 | Cytochrome C Antibody (YA6421) | WB, IHC-P, IHC-F, ICC/IF, IF-Tissue | Human, Mouse, Rat |
| HY-P86729A | Cytochrome C Antibody (YA6421)(PBS only) | WB, IHC-P, IHC-F, ICC/IF, IF-Tissue | Human, Mouse, Rat |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Thrombocytopenia 4 |
|
|
| Autosomal Thrombocytopenia With Normal Platelets |
|
|
| Thrombocytopenia |
|
|
| Ischemia |
|
|
| Liver Disease |
|
|
| Colorectal Cancer |
|
|
| Antley-Bixler Syndrome |
|
|
| Lung Cancer |
|
|
| Autosomal Dominant Optic Atrophy Plus Syndrome |
|
|
| Hepatoblastoma |
|
|
| Myeloid Leukemia |
|
|
| Nephrosclerosis |
|
|
| Hemangioma |
|
|
| Monocytic Leukemia |
|
|
| Prostate Cancer |
|
|
| Haemonchiasis |
|
|
| Parkinson Disease, Late-Onset |
|
|
| Acute Myocardial Infarction |
|
|
| Toxic Encephalopathy |
|
|
| Burkitt Lymphoma |
|
|
| Mitochondrial Complex Iv Deficiency, Nuclear Type 1 |
|
|
| Mitochondrial Encephalomyopathy |
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
|
| Pancreatic Cancer |
|
|
| Rhabdomyosarcoma |
|
|
| Acute Promyelocytic Leukemia |
|
|
| Colon Adenocarcinoma |
|
|
| 3-Methylglutaconic Aciduria, Type Iii |
|
|
| Cardiac Arrest |
|
|
| Hematologic Cancer |
|
|
| Macular Degeneration, Age-Related, 14 |
|
|
| Breast Cancer |
|
|
| Glioblastoma |
|
|
| Myocardial Infarction |
|
|
| Methemoglobinemia |
|
|
| Hepatocellular Carcinoma |
|
|
| Endometrial Cancer |
|
|
| Thyroid Gland Anaplastic Carcinoma |
|
|
| Pheochromocytoma |
|
|
| Myocardial Stunning |
|
|
| Neuroblastoma |
|
|
| Kearns-Sayre Syndrome |
|
|
| Barth Syndrome |
|
|
| Gastric Cancer |
|
|
| Ovarian Cancer |
|
|
| Stroke, Ischemic |
|
|
| Carotid Artery Occlusion |
|
|
| Melanoma |
|
|
| Friedreich Ataxia |
|
|
| T-Cell Acute Lymphoblastic Leukemia |
|
|
| Cataract |
|
|
| Leber Hereditary Optic Neuropathy, Modifier Of |
|
|
| Mitochondrial Complex Iii Deficiency, Nuclear Type 2 |
|
|
| Lung Cancer Susceptibility 3 |
|
|
| Osteogenic Sarcoma |
|
|
| Breast Adenocarcinoma |
|
|
| Autonomic Nervous System Neoplasm |
|
|
| Heart Disease |
|
|
| Mitochondrial Myopathy |
|
|
| Cranial Nerve Disease |
|
|
| Pulmonary Disease, Chronic Obstructive |
|
|
| Leukemia, Chronic Lymphocytic |
|
|
| Optic Nerve Disease |
|
|
| Huntington Disease |
|
|
| Peripheral Nervous System Neoplasm |
|
|
| Myeloma, Multiple |
|
|
| Diabetes Mellitus |
|
|
| Peripheral Nervous System Disease |
|
|
| Squamous Cell Carcinoma, Head And Neck |
|
|
| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes |
|
|
| Leigh Syndrome |
|
|
| Hypertension, Essential |
|
|
| Immune Deficiency Disease |
|
|
| Lymphoma, Non-Hodgkin, Familial |
|
|
| Mitochondrial Complex I Deficiency, Nuclear Type 1 |
|
|
| Nervous System Disease |
|
|
| Eye Disease |
|
|
| Leukemia, Acute Myeloid |
|
|
| Alzheimer Disease, Familial, 1 |
|
|
| Dilated Cardiomyopathy |
|
|
| Hypertrophic Cardiomyopathy |
|
|
| Retinitis Pigmentosa |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Mus musculus | CYCS | MGD | MGI:88578 |
| Canis familiaris | CYCS | VGNC | VGNC:50288 |
| Rattus norvegicus | CYCS | RGD | RGD:2451 |
| Others | CYCS | NCBI |