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 53126 - 53150 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0014544 Epilepsy SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0019061 Hemolytic-Uremic Syndrome SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0678222 Breast Carcinoma SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0206624 Hepatoblastoma SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0032460 Polycystic Ovary Syndrome SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0023467 Leukemia, Myelocytic, Acute SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C1834582 MYELOPROLIFERATIVE SYNDROME, TRANSIENT SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0036341 Schizophrenia SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0011615 Dermatitis, Atopic SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0271568 Laron Syndrome SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0013595 Eczema SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0028754 Obesity SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0018784 Sensorineural Hearing Loss (disorder) SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0035078 Kidney Failure SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0027651 Neoplasms SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0010054 Coronary Arteriosclerosis SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0004238 Atrial Fibrillation SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0011854 Diabetes Mellitus, Insulin-Dependent SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0027126 Myotonic Dystrophy SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0043119 Werner Syndrome SLC35G1 159371 solute carrier family 35 member G1 Q2M3R5
C0238052 Xanthomatosis, Cerebrotendinous CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0024523 Malabsorption Syndrome CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0302164 Tuberous xanthoma CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0600139 Prostate carcinoma CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318
C0524851 Neurodegenerative Disorders CYP27A1 1593 cytochrome P450 family 27 subfamily A member 1 Q02318

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Last updated: August 19, 2024