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 57026 - 57050 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C1328840 Autoimmune Lymphoproliferative Syndrome LYPLA1 10434 lysophospholipase 1 O75608
C0030297 Pancreatic Neoplasm LYPLA1 10434 lysophospholipase 1 O75608
C0011860 Diabetes Mellitus, Non-Insulin-Dependent LYPLA1 10434 lysophospholipase 1 O75608
C0600139 Prostate carcinoma LYPLA1 10434 lysophospholipase 1 O75608
C0006826 Malignant Neoplasms CLEC3A 10143 C-type lectin domain family 3 member A O75596
C1319315 Adenocarcinoma of large intestine CLEC3A 10143 C-type lectin domain family 3 member A O75596
C2675481 COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 CLEC3A 10143 C-type lectin domain family 3 member A O75596
C3554460 COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 CLEC3A 10143 C-type lectin domain family 3 member A O75596
C0007102 Malignant tumor of colon CLEC3A 10143 C-type lectin domain family 3 member A O75596
C0009402 Colorectal Carcinoma CLEC3A 10143 C-type lectin domain family 3 member A O75596
C0029408 Degenerative polyarthritis CLEC3A 10143 C-type lectin domain family 3 member A O75596
C0006142 Malignant neoplasm of breast CLEC3A 10143 C-type lectin domain family 3 member A O75596
C1306459 Primary malignant neoplasm CLEC3A 10143 C-type lectin domain family 3 member A O75596
C1837315 COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 CLEC3A 10143 C-type lectin domain family 3 member A O75596
C0024790 Paroxysmal nocturnal hemoglobinuria ECI2 10455 enoyl-CoA delta isomerase 2 O75521
C0600139 Prostate carcinoma ECI2 10455 enoyl-CoA delta isomerase 2 O75521
C0376358 Malignant neoplasm of prostate ECI2 10455 enoyl-CoA delta isomerase 2 O75521
C0002874 Aplastic Anemia ECI2 10455 enoyl-CoA delta isomerase 2 O75521
C0271907 Acquired aplastic anemia ECI2 10455 enoyl-CoA delta isomerase 2 O75521
C0027877 Neuronal Ceroid-Lipofuscinoses CLN5 1203 CLN5 intracellular trafficking protein O75503
C0751783 Lafora Disease CLN5 1203 CLN5 intracellular trafficking protein O75503
C1850442 CEROID LIPOFUSCINOSIS, NEURONAL, 5 CLN5 1203 CLN5 intracellular trafficking protein O75503
C1838571 Ceroid Lipofuscinosis, Neuronal, 7 CLN5 1203 CLN5 intracellular trafficking protein O75503
C0235946 Cerebral atrophy CLN5 1203 CLN5 intracellular trafficking protein O75503
C0022340 Late-Infantile Neuronal Ceroid Lipfuscinosis CLN5 1203 CLN5 intracellular trafficking protein O75503

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Last updated: August 19, 2024