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 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
---|---|---|---|---|---|
C0025958 | Microcephaly | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0015934 | Fetal Growth Retardation | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0019294 | Hernia, Inguinal | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C1261470 | Congenital meningocele | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C1837549 | SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2 | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0036439 | Scoliosis, unspecified | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0013336 | Dwarfism | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0029422 | Osteochondrodysplasias | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0080174 | Spina Bifida Occulta | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0848558 | Hypospadias | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C3714756 | Intellectual Disability | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0265677 | Congenital hemivertebra | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0002895 | Anemia, Sickle Cell | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C1306503 | Congenital exomphalos | LFNG | 3955 | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q8NES3 |
C0029408 | Degenerative polyarthritis | CHST13 | 166012 | carbohydrate sulfotransferase 13 | Q8NET6 |
C3203102 | Idiopathic pulmonary arterial hypertension | CHST13 | 166012 | carbohydrate sulfotransferase 13 | Q8NET6 |
C0152013 | Adenocarcinoma of lung (disorder) | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
C0006826 | Malignant Neoplasms | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
C0027651 | Neoplasms | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
C0242379 | Malignant neoplasm of lung | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
C0006142 | Malignant neoplasm of breast | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
C0678222 | Breast Carcinoma | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
C2239176 | Liver carcinoma | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
C0002895 | Anemia, Sickle Cell | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
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Last updated: August 19, 2024