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 8551 - 8575 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0023891 Liver Cirrhosis, Alcoholic MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0025362 Mental Retardation MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0524620 Metabolic Syndrome X MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0011849 Diabetes Mellitus MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C1263846 Attention deficit hyperactivity disorder MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0019158 Hepatitis MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0025958 Microcephaly MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0011847 Diabetes MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0751495 Seizures, Focal MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0684276 Hypsarrhythmia MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0023895 Liver diseases MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0020255 Hydrocephalus MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C1561643 Chronic Kidney Diseases MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0520947 Clumsiness - motor delay MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0023896 Alcoholic Liver Diseases MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0038273 Stereotypic Movement Disorder MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0007222 Cardiovascular Diseases MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0036857 Severe intellectual disability MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0028754 Obesity MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0024623 Malignant neoplasm of stomach MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0011581 Depressive disorder MBOAT7 79143 membrane bound O-acyltransferase domain containing 7 Q96N66
C0018784 Sensorineural Hearing Loss (disorder) ALG12 79087 ALG12 alpha-1,6-mannosyltransferase Q9BV10
C0235991 Small for gestational age (disorder) ALG12 79087 ALG12 alpha-1,6-mannosyltransferase Q9BV10
C0010417 Cryptorchidism ALG12 79087 ALG12 alpha-1,6-mannosyltransferase Q9BV10
C0009081 Congenital clubfoot ALG12 79087 ALG12 alpha-1,6-mannosyltransferase Q9BV10

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Last updated: August 19, 2024