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 56251 - 56275 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0022658 Kidney Diseases ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0036341 Schizophrenia ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0024143 Lupus Nephritis ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0005697 Neurogenic Urinary Bladder ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0025958 Microcephaly ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0007131 Non-Small Cell Lung Carcinoma ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0494475 Tonic - clonic seizures ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0038454 Cerebrovascular accident ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C3714542 Lymphoma, Diffuse ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0036572 Seizures ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0022336 Creutzfeldt-Jakob disease ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0015300 Exophthalmos ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C1862939 AMYOTROPHIC LATERAL SCLEROSIS 1 ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0020619 Hypogonadism ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0751495 Seizures, Focal ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0242379 Malignant neoplasm of lung ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0006826 Malignant Neoplasms ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0206650 Fibroadenoma ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0015934 Fetal Growth Retardation ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0684249 Carcinoma of lung ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0019829 Hodgkin Disease ALG1 56052 ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase Q9BT22
C0016667 Fragile X Syndrome INPP5K 51763 inositol polyphosphate-5-phosphatase K Q9BT40
C1956346 Coronary Artery Disease INPP5K 51763 inositol polyphosphate-5-phosphatase K Q9BT40
C0699893 Skin carcinoma INPP5K 51763 inositol polyphosphate-5-phosphatase K Q9BT40
C0678222 Breast Carcinoma INPP5K 51763 inositol polyphosphate-5-phosphatase K Q9BT40

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Last updated: August 19, 2024