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 62226 - 62250 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0002871 Anemia TMED3 23423 transmembrane p24 trafficking protein 3 Q9Y3Q3
C0398791 Nijmegen Breakage Syndrome TMED3 23423 transmembrane p24 trafficking protein 3 Q9Y3Q3
C2239176 Liver carcinoma TMED3 23423 transmembrane p24 trafficking protein 3 Q9Y3Q3
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma TMED3 23423 transmembrane p24 trafficking protein 3 Q9Y3Q3
C0006142 Malignant neoplasm of breast TMED3 23423 transmembrane p24 trafficking protein 3 Q9Y3Q3
C0376358 Malignant neoplasm of prostate TMED3 23423 transmembrane p24 trafficking protein 3 Q9Y3Q3
C0035334 Retinitis Pigmentosa TMED3 23423 transmembrane p24 trafficking protein 3 Q9Y3Q3
C0035412 Rhabdomyosarcoma NEU2 4759 neuraminidase 2 Q9Y3R4
C0699791 Stomach Carcinoma NEU2 4759 neuraminidase 2 Q9Y3R4
C0600139 Prostate carcinoma NEU2 4759 neuraminidase 2 Q9Y3R4
C0027651 Neoplasms NEU2 4759 neuraminidase 2 Q9Y3R4
C1335302 Pancreatic Ductal Adenocarcinoma NEU2 4759 neuraminidase 2 Q9Y3R4
C0024623 Malignant neoplasm of stomach NEU2 4759 neuraminidase 2 Q9Y3R4
C2607914 Allergic rhinitis (disorder) NEU2 4759 neuraminidase 2 Q9Y3R4
C0376358 Malignant neoplasm of prostate NEU2 4759 neuraminidase 2 Q9Y3R4
C0235974 Pancreatic carcinoma NEU2 4759 neuraminidase 2 Q9Y3R4
C0010495 Cutis Laxa ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C0027092 Myopia ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C4479409 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C0852949 Arteriopathic disease ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C0007766 Intracranial Aneurysm ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C1318518 Infantile malignant osteopetrosis ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C0432255 Geroderma osteodysplastica ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C0575158 Kyphoscoliosis deformity of spine ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487
C0004153 Atherosclerosis ATP6V0A2 23545 ATPase H+ transporting V0 subunit a2 Q9Y487

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Last updated: August 19, 2024