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 53776 - 53800 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C1275126 TNF receptor-associated periodic fever syndrome (TRAPS) SIGLEC7 27036 sialic acid binding Ig like lectin 7 Q9Y286
C1275126 TNF receptor-associated periodic fever syndrome (TRAPS) PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
C1275126 TNF receptor-associated periodic fever syndrome (TRAPS) CD14 929 CD14 molecule P08571
C1275126 TNF receptor-associated periodic fever syndrome (TRAPS) PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C1275126 TNF receptor-associated periodic fever syndrome (TRAPS) IL18R1 8809 interleukin 18 receptor 1 Q13478
C1275126 TNF receptor-associated periodic fever syndrome (TRAPS) PIK3CB 5291 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta P42338
C1275126 TNF receptor-associated periodic fever syndrome (TRAPS) PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C1275273 Familial Multiple Lipomatosis PTEN 5728 phosphatase and tensin homolog P60484
C1275278 Extraskeletal Myxoid Chondrosarcoma PTEN 5728 phosphatase and tensin homolog P60484
C1275668 Melanotic medulloblastoma PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C1275685 Avellino corneal dystrophy PARP1 142 poly(ADP-ribose) polymerase 1 P09874
C1275685 Avellino corneal dystrophy SDC1 6382 syndecan 1 P18827
C1275685 Avellino corneal dystrophy ACE 1636 angiotensin I converting enzyme P12821
C1275685 Avellino corneal dystrophy GCDH 2639 glutaryl-CoA dehydrogenase Q92947
C1275685 Avellino corneal dystrophy CAT 847 catalase P04040
C1275685 Avellino corneal dystrophy CD1D 912 CD1d molecule P15813
C1275685 Avellino corneal dystrophy LPIN2 9663 lipin 2 Q92539
C1275808 Congenital central hypoventilation SLC2A10 81031 solute carrier family 2 member 10 O95528
C1276035 Pena-Shokeir syndrome type I DPAGT1 1798 dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 Q9H3H5
C1276035 Pena-Shokeir syndrome type I PIGS 94005 phosphatidylinositol glycan anchor biosynthesis class S Q96S52
C1276035 Pena-Shokeir syndrome type I GBA 2629 glucosylceramidase beta P04062
C1276035 Pena-Shokeir syndrome type I GBE1 2632 1,4-alpha-glucan branching enzyme 1 Q04446
C1276035 Pena-Shokeir syndrome type I PDHA1 5160 pyruvate dehydrogenase E1 subunit alpha 1 P08559
C1276035 Pena-Shokeir syndrome type I AGRN 375790 agrin O00468
C1276035 Pena-Shokeir syndrome type I CNTN1 1272 contactin 1 Q12860

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Last updated: August 19, 2024