DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 57226 - 57250 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0007102 Malignant tumor of colon MACROD2 140733 mono-ADP ribosylhydrolase 2 A1Z1Q3
C0009402 Colorectal Carcinoma MACROD2 140733 mono-ADP ribosylhydrolase 2 A1Z1Q3
C0023467 Leukemia, Myelocytic, Acute MACROD2 140733 mono-ADP ribosylhydrolase 2 A1Z1Q3
C1306459 Primary malignant neoplasm MACROD2 140733 mono-ADP ribosylhydrolase 2 A1Z1Q3
C0023903 Liver neoplasms MACROD2 140733 mono-ADP ribosylhydrolase 2 A1Z1Q3
C3808986 HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA MACROD2 140733 mono-ADP ribosylhydrolase 2 A1Z1Q3
C0740858 Substance abuse problem MACROD2 140733 mono-ADP ribosylhydrolase 2 A1Z1Q3
C0038586 Substance Use Disorders MACROD2 140733 mono-ADP ribosylhydrolase 2 A1Z1Q3
C1510472 Drug Dependence MACROD2 140733 mono-ADP ribosylhydrolase 2 A1Z1Q3
C0009402 Colorectal Carcinoma GCNT7 140687 glucosaminyl (N-acetyl) transferase family member 7 Q6ZNI0
C1837461 SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 CHODL 140578 chondrolectin Q9H9P2
C0007131 Non-Small Cell Lung Carcinoma CHODL 140578 chondrolectin Q9H9P2
C0684249 Carcinoma of lung CHODL 140578 chondrolectin Q9H9P2
C2267227 Bulimia Nervosa CHODL 140578 chondrolectin Q9H9P2
C0026847 Spinal Muscular Atrophy CHODL 140578 chondrolectin Q9H9P2
C0027651 Neoplasms CHODL 140578 chondrolectin Q9H9P2
C0848558 Hypospadias DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0520947 Clumsiness - motor delay DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0004930 Behavior Disorders DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0600139 Prostate carcinoma DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0016667 Fragile X Syndrome DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C2239176 Liver carcinoma DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0000768 Congenital Abnormality DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0010068 Coronary heart disease DGKK 139189 diacylglycerol kinase kappa Q5KSL6
C0036857 Severe intellectual disability DGKK 139189 diacylglycerol kinase kappa Q5KSL6

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Last updated: August 19, 2024