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 41101 - 41125 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0524662 Opiate Addiction PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C0035222 Respiratory Distress Syndrome, Adult PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C0040517 Gilles de la Tourette syndrome PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C0021400 Influenza PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C0155877 Allergic asthma PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C0017536 Giardiasis PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C0751606 Adult Acute Lymphocytic Leukemia PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C0005586 Bipolar Disorder PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C0027947 Neutropenia PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C1850900 Familial primary gastric lymphoma PARP9 83666 poly(ADP-ribose) polymerase family member 9 Q8IXQ6
C0039101 synovial sarcoma PC 5091 pyruvate carboxylase P11498
C0002875 Cooley's anemia PC 5091 pyruvate carboxylase P11498
C1306459 Primary malignant neoplasm PC 5091 pyruvate carboxylase P11498
C0010068 Coronary heart disease PC 5091 pyruvate carboxylase P11498
C1861172 Venous Thromboembolism PC 5091 pyruvate carboxylase P11498
C0020456 Hyperglycemia PC 5091 pyruvate carboxylase P11498
C0011860 Diabetes Mellitus, Non-Insulin-Dependent PC 5091 pyruvate carboxylase P11498
C0268553 Hyperlysinemias PC 5091 pyruvate carboxylase P11498
C0311370 Lupus anticoagulant disorder PC 5091 pyruvate carboxylase P11498
C0006142 Malignant neoplasm of breast PC 5091 pyruvate carboxylase P11498
C0153452 Malignant neoplasm of gallbladder PC 5091 pyruvate carboxylase P11498
C0034341 Pyruvate Carboxylase Deficiency Disease PC 5091 pyruvate carboxylase P11498
C3714756 Intellectual Disability PC 5091 pyruvate carboxylase P11498
C0085650 Purpura Fulminans PC 5091 pyruvate carboxylase P11498
C0003850 Arteriosclerosis PC 5091 pyruvate carboxylase P11498

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Last updated: August 19, 2024