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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 9801 - 9825 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0206754 Neuroendocrine Tumors DAD1 1603 defender against cell death 1 P61803
C0264408 Childhood asthma DAD1 1603 defender against cell death 1 P61803
C0149925 Small cell carcinoma of lung DAD1 1603 defender against cell death 1 P61803
C1306459 Primary malignant neoplasm DAD1 1603 defender against cell death 1 P61803
C0004763 Barrett Esophagus DAD1 1603 defender against cell death 1 P61803
C0155877 Allergic asthma DAD1 1603 defender against cell death 1 P61803
C0006826 Malignant Neoplasms DAD1 1603 defender against cell death 1 P61803
C0018784 Sensorineural Hearing Loss (disorder) TMTC2 160335 transmembrane O-mannosyltransferase targeting cadherins 2 Q8N394
C0152136 Low Tension Glaucoma TMTC2 160335 transmembrane O-mannosyltransferase targeting cadherins 2 Q8N394
C0017601 Glaucoma TMTC2 160335 transmembrane O-mannosyltransferase targeting cadherins 2 Q8N394
C0013595 Eczema TMTC2 160335 transmembrane O-mannosyltransferase targeting cadherins 2 Q8N394
C0004096 Asthma TMTC2 160335 transmembrane O-mannosyltransferase targeting cadherins 2 Q8N394
C4082305 Deaf Mutism TMTC2 160335 transmembrane O-mannosyltransferase targeting cadherins 2 Q8N394
C0339573 Glaucoma, Primary Open Angle TMTC2 160335 transmembrane O-mannosyltransferase targeting cadherins 2 Q8N394
C0011053 Deafness TMTC2 160335 transmembrane O-mannosyltransferase targeting cadherins 2 Q8N394
C0023467 Leukemia, Myelocytic, Acute CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
C0023465 Acute monocytic leukemia CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
C0023473 Myeloid Leukemia, Chronic CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
C1332977 Childhood Leukemia CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
C0021053 Immune System Diseases CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
C0023418 leukemia CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
C0014070 Encephalomyelitis CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
C1306459 Primary malignant neoplasm CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
C0026946 Mycoses CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
C0026470 Monoclonal Gammopathy of Undetermined Significance CLEC12A 160364 C-type lectin domain family 12 member A Q5QGZ9
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Last updated: August 19, 2024