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 46551 - 46575 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C0410203 X-linked centronuclear myopathy MTMR2 8898 myotubularin related protein 2 Q13614
C0410207 Tubular Aggregate Myopathy GFPT1 2673 glutamine--fructose-6-phosphate transaminase 1 Q06210
C0410207 Tubular Aggregate Myopathy OVGP1 5016 oviductal glycoprotein 1 Q12889
C0410207 Tubular Aggregate Myopathy CLEC10A 10462 C-type lectin domain containing 10A Q8IUN9
C0410207 Tubular Aggregate Myopathy MTMR14 64419 myotubularin related protein 14 Q8NCE2
C0410207 Tubular Aggregate Myopathy SIRT4 23409 sirtuin 4 Q9Y6E7
C0410207 Tubular Aggregate Myopathy CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0410207 Tubular Aggregate Myopathy MTM1 4534 myotubularin 1 Q13496
C0410422 Chronic multifocal osteomyelitis PIGN 23556 phosphatidylinositol glycan anchor biosynthesis class N O95427
C0410422 Chronic multifocal osteomyelitis RPE 6120 ribulose-5-phosphate-3-epimerase Q96AT9
C0410422 Chronic multifocal osteomyelitis CPT1B 1375 carnitine palmitoyltransferase 1B Q92523
C0410422 Chronic multifocal osteomyelitis LPIN2 9663 lipin 2 Q92539
C0410529 Hypochondroplasia (disorder) GALNT2 2590 polypeptide N-acetylgalactosaminyltransferase 2 Q10471
C0410530 Metachondromatosis EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0410530 Metachondromatosis EXT1 2131 exostosin glycosyltransferase 1 Q16394
C0410530 Metachondromatosis DPEP1 1800 dipeptidase 1 P16444
C0410538 Pseudoachondroplasia CANX 821 calnexin P27824
C0410538 Pseudoachondroplasia DCN 1634 decorin P07585
C0410538 Pseudoachondroplasia ACAN 176 aggrecan P16112
C0410538 Pseudoachondroplasia COL9A2 1298 collagen type IX alpha 2 chain Q14055
C0410574 Synovial Hypertrophy SCD 6319 stearoyl-CoA desaturase O00767
C0410606 Cervical Disc Degenerative Disorder ACAN 176 aggrecan P16112
C0423775 Scurfiness of scalp CYP51A1 1595 cytochrome P450 family 51 subfamily A member 1 Q16850
C0426970 Spastic Quadriplegia FUCA1 2517 alpha-L-fucosidase 1 P04066
C0426970 Spastic Quadriplegia GLB1 2720 galactosidase beta 1 P16278

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Last updated: August 19, 2024