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 46101 - 46125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C3495498 Cardiomyopathy, Familial Hypertrophic, 1 (disorder) CALR3 125972 calreticulin 3 Q96L12
C1306459 Primary malignant neoplasm CALR 811 calreticulin P27797
C0040028 Thrombocythemia, Essential CALR 811 calreticulin P27797
C0029172 Oral Submucous Fibrosis CALR 811 calreticulin P27797
C1527336 Sjogren's Syndrome CALR 811 calreticulin P27797
C0025202 melanoma CALR 811 calreticulin P27797
C0278878 Adult Glioblastoma CALR 811 calreticulin P27797
C0027651 Neoplasms CALR 811 calreticulin P27797
C2931822 Nasopharyngeal carcinoma CALR 811 calreticulin P27797
C0006826 Malignant Neoplasms CALR 811 calreticulin P27797
C1292778 Chronic myeloproliferative disorder CALR 811 calreticulin P27797
C0001815 Primary Myelofibrosis CALR 811 calreticulin P27797
C0677886 Epithelial ovarian cancer CALR 811 calreticulin P27797
C0684249 Carcinoma of lung CALR 811 calreticulin P27797
C1175175 Severe Acute Respiratory Syndrome CALR 811 calreticulin P27797
C0007102 Malignant tumor of colon CALR 811 calreticulin P27797
C0018824 Heart valve disease CALR 811 calreticulin P27797
C0836924 Thrombocytosis CALR 811 calreticulin P27797
C0678222 Breast Carcinoma CALR 811 calreticulin P27797
C0027022 Myeloproliferative disease CALR 811 calreticulin P27797
C0080024 Piebaldism CALR 811 calreticulin P27797
C0546837 Malignant neoplasm of esophagus CALR 811 calreticulin P27797
C0003873 Rheumatoid Arthritis CALR 811 calreticulin P27797
C0018801 Heart failure CALR 811 calreticulin P27797
C0023452 Childhood Acute Lymphoblastic Leukemia CALR 811 calreticulin P27797

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Last updated: August 19, 2024