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 61626 - 61650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C1378511 Undifferentiated leukemia CD38 952 CD38 molecule P28907
C0007570 Celiac Disease CD38 952 CD38 molecule P28907
C0037926 Compression of spinal cord CD38 952 CD38 molecule P28907
C0023493 Adult T-Cell Lymphoma/Leukemia CD38 952 CD38 molecule P28907
C4048328 cervical cancer CD38 952 CD38 molecule P28907
C0005283 beta Thalassemia CD38 952 CD38 molecule P28907
C0022283 Incontinentia Pigmenti Achromians CD38 952 CD38 molecule P28907
C0036310 Scheuermann's Disease CD38 952 CD38 molecule P28907
C0003486 Aortic Aneurysm CD38 952 CD38 molecule P28907
C0036572 Seizures CD38 952 CD38 molecule P28907
C1263846 Attention deficit hyperactivity disorder CD38 952 CD38 molecule P28907
C0024314 Lymphoproliferative Disorders CD38 952 CD38 molecule P28907
C0162678 Neurofibromatoses CD38 952 CD38 molecule P28907
C0013336 Dwarfism CD38 952 CD38 molecule P28907
C0026705 Mucopolysaccharidosis II CD38 952 CD38 molecule P28907
C0023462 Acute Megakaryocytic Leukemias CD38 952 CD38 molecule P28907
C0029434 Osteogenesis Imperfecta CD38 952 CD38 molecule P28907
C0036439 Scoliosis, unspecified CD38 952 CD38 molecule P28907
C0021400 Influenza CD38 952 CD38 molecule P28907
C0278878 Adult Glioblastoma CD38 952 CD38 molecule P28907
C0013421 Dystonia TECR 9524 trans-2,3-enoyl-CoA reductase Q9NZ01
C0000768 Congenital Abnormality TECR 9524 trans-2,3-enoyl-CoA reductase Q9NZ01
C0025362 Mental Retardation TECR 9524 trans-2,3-enoyl-CoA reductase Q9NZ01
C0235946 Cerebral atrophy TECR 9524 trans-2,3-enoyl-CoA reductase Q9NZ01
C0038273 Stereotypic Movement Disorder TECR 9524 trans-2,3-enoyl-CoA reductase Q9NZ01

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Last updated: August 19, 2024