Showing entry for Gamma-crystallin C


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT026109
Protein NameGamma-crystallin C
Uniport IdP07315
GeneCRYGC
Gene Id1420
DomainCrystall
Pfam PF00030  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0002088 lens development in camera-type eye
Biological Process GO:0007601 visual perception
molecular function GO:0005212 structural constituent of eye lens
cellular component GO:0005737 cytoplasm
cellular component GO:0005634 nucleus
Reactome
Pathway Id Pathway Name
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0002418 BXGD000112 Amblyopia Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0003507 BXGD000203 Aortic Valve Stenosis Cardiovascular Diseases
C0004096 BXGD000252 Asthma Respiratory Tract Diseases; Immune System Diseases
C0004238 BXGD000262 Atrial Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007102 BXGD000425 Malignant tumor of colon Digestive System Diseases; Neoplasms
C0009402 BXGD000605 Colorectal Carcinoma Digestive System Diseases; Neoplasms
C0009691 BXGD000622 Congenital cataract Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Nervous System Diseases
C0010036 BXGD000642 Corneal dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0010038 BXGD000643 Corneal Opacity Eye Diseases
C0014457 BXGD000915 Eosinophilia Hemic and Lymphatic Diseases
C0018801 BXGD001226 Heart failure Cardiovascular Diseases
C0018802 BXGD001227 Congestive heart failure Cardiovascular Diseases
C0021051 BXGD001475 Immunologic Deficiency Syndromes Immune System Diseases
C0022346 BXGD001537 Icterus Pathological Conditions, Signs and Symptoms
C0023434 BXGD001643 Chronic Lymphocytic Leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024117 BXGD001734 Chronic Obstructive Airway Disease Respiratory Tract Diseases
C0024141 BXGD001740 Lupus Erythematosus, Systemic Skin and Connective Tissue Diseases; Immune System Diseases
C0026010 BXGD001886 Microphthalmos Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0026769 BXGD001930 Multiple Sclerosis Immune System Diseases; Nervous System Diseases
C0027092 BXGD001971 Myopia Eye Diseases
C0027651 BXGD002009 Neoplasms Neoplasms
C0027819 BXGD002043 Neuroblastoma Neoplasms
C0028738 BXGD002081 Nystagmus Eye Diseases; Nervous System Diseases
C0029882 BXGD002177 Otitis Media Otorhinolaryngologic Diseases
C0035304 BXGD002528 Retinal Degeneration Eye Diseases
C0041296 BXGD002903 Tuberculosis Infections
C0086543 BXGD003294 Cataract Eye Diseases
C0151650 BXGD003454 Renal fibrosis Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0158551 BXGD003890 Embryonal nuclear cataract (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0240063 BXGD005015 Coloboma of iris Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0264716 BXGD005417 Chronic heart failure Cardiovascular Diseases
C0266544 BXGD005691 Microcornea Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0266551 BXGD005693 Congenital coloboma of iris Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0376358 BXGD007992 Malignant neoplasm of prostate Neoplasms; Male Urogenital Diseases
C0392557 BXGD008056 Nuclear cataract Eye Diseases
C0521707 BXGD009166 Bilateral cataracts (disorder) Eye Diseases
C0524524 BXGD009228 Pseudoaphakia Eye Diseases
C0600139 BXGD009695 Prostate carcinoma Neoplasms; Male Urogenital Diseases
C0699790 BXGD009866 Colon Carcinoma Digestive System Diseases; Neoplasms
C0700095 BXGD009875 Central neuroblastoma Neoplasms; Nervous System Diseases
C0742343 BXGD010061 Acute Chest Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases
C1112705 BXGD011681 Nuclear non-senile cataract Eye Diseases
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1306759 BXGD012374 Eosinophilic disorder Hemic and Lymphatic Diseases
C1510497 BXGD013174 Lens Opacities Eye Diseases
C1527287 BXGD013263 Acanthocheilonemiasis Infections
C1833118 BXGD013897 Cataract, Pulverulent Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C1852438 BXGD015281 CATARACT, COPPOCK-LIKE Eye Diseases
C1858679 BXGD015818 CATARACT, AUTOSOMAL DOMINANT Eye Diseases
C1861829 BXGD016080 Cataract microcornea syndrome Eye Diseases
C1868683 BXGD016526 B-CELL MALIGNANCY, LOW-GRADE
C1963184 BXGD016688 Nystagmus, CTCAE 3.0
C2363741 BXGD017100 HIV-1 infection
C2827407 BXGD017795 Infectious Otitis Media Otorhinolaryngologic Diseases
C4015995 BXGD020255 CATARACT 2, COPPOCK-LIKE
C4086165 BXGD022126 Childhood Neuroblastoma Neoplasms
C4554036 BXGD023557 Nystagmus, CTCAE 5.0
C4721890 BXGD023782 CATARACT 2, MULTIPLE TYPES
C4722085 BXGD023788 Malignant neoplasm of colon and/or rectum
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0006990 Lanosterol 426.72
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein