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 58051 - 58075 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0033860 Psoriasis IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C2607914 Allergic rhinitis (disorder) IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C0011603 Dermatitis IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C3875321 Inflammatory dermatosis IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C0162836 Hidradenitis Suppurativa IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C0019569 Hirschsprung Disease IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C0152081 Pustular psoriasis IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C0029408 Degenerative polyarthritis IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C0009324 Ulcerative Colitis IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C0009319 Colitis IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C0019196 Hepatitis C IL1RL2 8808 interleukin 1 receptor like 2 Q9HB29
C0036631 Seminoma ETNK1 55500 ethanolamine kinase 1 Q9HBU6
C1540912 Hypereosinophilic syndrome ETNK1 55500 ethanolamine kinase 1 Q9HBU6
C1292772 Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative ETNK1 55500 ethanolamine kinase 1 Q9HBU6
C0221013 Mastocytosis, Systemic ETNK1 55500 ethanolamine kinase 1 Q9HBU6
C0349639 Juvenile Myelomonocytic Leukemia ETNK1 55500 ethanolamine kinase 1 Q9HBU6
C0023480 Leukemia, Myelomonocytic, Chronic ETNK1 55500 ethanolamine kinase 1 Q9HBU6
C0027651 Neoplasms ETNK1 55500 ethanolamine kinase 1 Q9HBU6
C0014457 Eosinophilia ETNK1 55500 ethanolamine kinase 1 Q9HBU6
C3553571 Carbohydrate deficient glycoprotein syndrome type 2k TMEM165 55858 transmembrane protein 165 Q9HC07
C0575158 Kyphoscoliosis deformity of spine TMEM165 55858 transmembrane protein 165 Q9HC07
C0241005 Creatine phosphokinase serum increased TMEM165 55858 transmembrane protein 165 Q9HC07
C0011989 Camurati-Engelmann Syndrome TMEM165 55858 transmembrane protein 165 Q9HC07
C1306459 Primary malignant neoplasm TMEM165 55858 transmembrane protein 165 Q9HC07
C0002452 Amelogenesis Imperfecta TMEM165 55858 transmembrane protein 165 Q9HC07

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Last updated: August 19, 2024