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 3526 - 3550 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0023890 Liver Cirrhosis CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0019163 Hepatitis B CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0262587 Parathyroid Adenoma CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0005695 Bladder Neoplasm CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C1458155 Mammary Neoplasms CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0878544 Cardiomyopathies CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0403766 Acquired phimosis CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0013336 Dwarfism CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0238461 Anaplastic thyroid carcinoma CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0033975 Psychotic Disorders CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0013595 Eczema CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0015230 Exanthema CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C1135196 Heart Failure, Diastolic CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0162311 Androgenetic Alopecia CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0027720 Nephrosis CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0030567 Parkinson Disease CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0027709 Nephrocalcinosis CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0001403 Addison Disease CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0007114 Malignant neoplasm of skin CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0039621 Tetany CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C1332986 Childhood Osteosarcoma CYP27B1 1594 cytochrome P450 family 27 subfamily B member 1 O15528
C0004782 Basal Ganglia Diseases ST8SIA3 51046 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 O43173
C0006826 Malignant Neoplasms ST8SIA3 51046 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 O43173
C0036341 Schizophrenia ST8SIA3 51046 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 O43173

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Last updated: August 19, 2024