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 11651 - 11675 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0027404 Narcolepsy MDGA2 161357 MAM domain containing glycosylphosphatidylinositol anchor 2 Q7Z553
C0699791 Stomach Carcinoma MDGA2 161357 MAM domain containing glycosylphosphatidylinositol anchor 2 Q7Z553
C0376532 Epilepsy, Rolandic MDGA2 161357 MAM domain containing glycosylphosphatidylinositol anchor 2 Q7Z553
C0011334 Dental caries LYZL2 119180 lysozyme like 2 Q7Z4W2
C2239176 Liver carcinoma DCXR 51181 dicarbonyl and L-xylulose reductase Q7Z4W1
C0008533 Hemophilia B DCXR 51181 dicarbonyl and L-xylulose reductase Q7Z4W1
C0376358 Malignant neoplasm of prostate DCXR 51181 dicarbonyl and L-xylulose reductase Q7Z4W1
C0268162 Pentosuria DCXR 51181 dicarbonyl and L-xylulose reductase Q7Z4W1
C0007097 Carcinoma DCXR 51181 dicarbonyl and L-xylulose reductase Q7Z4W1
C0027651 Neoplasms DCXR 51181 dicarbonyl and L-xylulose reductase Q7Z4W1
C0003864 Arthritis DCXR 51181 dicarbonyl and L-xylulose reductase Q7Z4W1
C0007112 Adenocarcinoma of prostate DCXR 51181 dicarbonyl and L-xylulose reductase Q7Z4W1
C0278701 Gastric Adenocarcinoma GALNTL5 168391 polypeptide N-acetylgalactosaminyltransferase like 5 Q7Z4T8
C0037274 Dermatologic disorders GALNTL5 168391 polypeptide N-acetylgalactosaminyltransferase like 5 Q7Z4T8
C0021364 Male infertility GALNTL5 168391 polypeptide N-acetylgalactosaminyltransferase like 5 Q7Z4T8
C0600298 Periodontosis GLT6D1 360203 glycosyltransferase 6 domain containing 1 Q7Z4J2
C0001342 Acute periodontitis GLT6D1 360203 glycosyltransferase 6 domain containing 1 Q7Z4J2
C0031106 Aggressive Periodontitis GLT6D1 360203 glycosyltransferase 6 domain containing 1 Q7Z4J2
C0031099 Periodontitis GLT6D1 360203 glycosyltransferase 6 domain containing 1 Q7Z4J2
C2242776 Plexiform leiomyoma POGLUT3 143888 protein O-glucosyltransferase 3 Q7Z4H8
C0007134 Renal Cell Carcinoma POGLUT3 143888 protein O-glucosyltransferase 3 Q7Z4H8
C0034152 Henoch-Schoenlein Purpura CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0037773 Spastic Paraplegia, Hereditary CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0524851 Neurodegenerative Disorders CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0037772 Spastic Paraplegia CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449

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Last updated: August 19, 2024