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 52551 - 52575 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C1863655 Deafness, Autosomal Recessive 21 TECTA 7007 tectorin alpha O75443
C0006142 Malignant neoplasm of breast TECTA 7007 tectorin alpha O75443
C0452138 Sensorineural hearing loss, bilateral TECTA 7007 tectorin alpha O75443
C0271514 Low frequency deafness TECTA 7007 tectorin alpha O75443
C1838701 DEAFNESS, AUTOSOMAL RECESSIVE 2 TECTA 7007 tectorin alpha O75443
C4048328 cervical cancer TKT 7086 transketolase P29401
C0011860 Diabetes Mellitus, Non-Insulin-Dependent TKT 7086 transketolase P29401
C1306459 Primary malignant neoplasm TKT 7086 transketolase P29401
C0036341 Schizophrenia TKT 7086 transketolase P29401
C0001973 Alcoholic Intoxication, Chronic TKT 7086 transketolase P29401
C0152025 Polyneuropathy TKT 7086 transketolase P29401
C0027651 Neoplasms TKT 7086 transketolase P29401
C0699790 Colon Carcinoma TKT 7086 transketolase P29401
C1851585 MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA TKT 7086 transketolase P29401
C0238461 Anaplastic thyroid carcinoma TKT 7086 transketolase P29401
C0349464 Wernicke-Korsakoff Syndrome TKT 7086 transketolase P29401
C0043121 Wernicke Encephalopathy TKT 7086 transketolase P29401
C0039841 Thiamine Deficiency TKT 7086 transketolase P29401
C3714756 Intellectual Disability TKT 7086 transketolase P29401
C0018818 Ventricular Septal Defects TKT 7086 transketolase P29401
C2239176 Liver carcinoma TKT 7086 transketolase P29401
C2931822 Nasopharyngeal carcinoma TKT 7086 transketolase P29401
C0699791 Stomach Carcinoma TKT 7086 transketolase P29401
C0006826 Malignant Neoplasms TKT 7086 transketolase P29401
C4721610 Carcinoma, Ovarian Epithelial TKT 7086 transketolase P29401

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Last updated: August 19, 2024