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 60876 - 60900 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0027051 Myocardial Infarction B3GNT2 10678 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 Q9NY97
C0376358 Malignant neoplasm of prostate B3GNT2 10678 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 Q9NY97
C0033860 Psoriasis B3GNT2 10678 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 Q9NY97
C0007138 Carcinoma, Transitional Cell B3GNT2 10678 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 Q9NY97
C0036341 Schizophrenia CSPG5 10675 chondroitin sulfate proteoglycan 5 O95196
C0175695 Sotos' syndrome CSPG5 10675 chondroitin sulfate proteoglycan 5 O95196
C0011311 Dengue Fever CSPG5 10675 chondroitin sulfate proteoglycan 5 O95196
C0025202 melanoma ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C0006826 Malignant Neoplasms ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C1458155 Mammary Neoplasms ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C0027651 Neoplasms ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C0017661 IGA Glomerulonephritis ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C0009402 Colorectal Carcinoma ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C0006142 Malignant neoplasm of breast ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C0678222 Breast Carcinoma ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C0206682 Follicular thyroid carcinoma ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C1269683 Major Depressive Disorder ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C1306459 Primary malignant neoplasm ST6GALNAC2 10610 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 Q9UJ37
C3150415 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 POMT1 10585 protein O-mannosyltransferase 1 Q9Y6A1
C0265221 Walker-Warburg congenital muscular dystrophy POMT1 10585 protein O-mannosyltransferase 1 Q9Y6A1
C0038379 Strabismus POMT1 10585 protein O-mannosyltransferase 1 Q9Y6A1
C0686353 Muscular Dystrophies, Limb-Girdle POMT1 10585 protein O-mannosyltransferase 1 Q9Y6A1
C0699743 Congenital muscular dystrophy (disorder) POMT1 10585 protein O-mannosyltransferase 1 Q9Y6A1
C0006118 Brain Neoplasms POMT1 10585 protein O-mannosyltransferase 1 Q9Y6A1
C3714756 Intellectual Disability POMT1 10585 protein O-mannosyltransferase 1 Q9Y6A1

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