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 58576 - 58600 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C1868683 B-CELL MALIGNANCY, LOW-GRADE FCGR3B 2215 Fc fragment of IgG receptor IIIb O75015
C1868683 B-CELL MALIGNANCY, LOW-GRADE SIGLEC7 27036 sialic acid binding Ig like lectin 7 Q9Y286
C1868683 B-CELL MALIGNANCY, LOW-GRADE HMMR 3161 hyaluronan mediated motility receptor O75330
C1868683 B-CELL MALIGNANCY, LOW-GRADE ANXA5 308 annexin A5 P08758
C1868683 B-CELL MALIGNANCY, LOW-GRADE LPL 4023 lipoprotein lipase P06858
C1868683 B-CELL MALIGNANCY, LOW-GRADE NT5E 4907 5'-nucleotidase ecto P21589
C1868683 B-CELL MALIGNANCY, LOW-GRADE ISYNA1 51477 inositol-3-phosphate synthase 1 Q9NPH2
C1868683 B-CELL MALIGNANCY, LOW-GRADE PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
C1868683 B-CELL MALIGNANCY, LOW-GRADE SELL 6402 selectin L P14151
C1868683 B-CELL MALIGNANCY, LOW-GRADE CD1D 912 CD1d molecule P15813
C1868683 B-CELL MALIGNANCY, LOW-GRADE CD74 972 CD74 molecule P04233
C1868683 B-CELL MALIGNANCY, LOW-GRADE PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C1868683 B-CELL MALIGNANCY, LOW-GRADE IL18R1 8809 interleukin 18 receptor 1 Q13478
C1868683 B-CELL MALIGNANCY, LOW-GRADE CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C1868683 B-CELL MALIGNANCY, LOW-GRADE PIK3CB 5291 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta P42338
C1868683 B-CELL MALIGNANCY, LOW-GRADE PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C1868683 B-CELL MALIGNANCY, LOW-GRADE PTEN 5728 phosphatase and tensin homolog P60484
C1868683 B-CELL MALIGNANCY, LOW-GRADE SULT1E1 6783 sulfotransferase family 1E member 1 P49888
C1868684 EAR, PATELLA, SHORT STATURE SYNDROME COMT 1312 catechol-O-methyltransferase P21964
C1868684 EAR, PATELLA, SHORT STATURE SYNDROME LYZ 4069 lysozyme P61626
C1868684 EAR, PATELLA, SHORT STATURE SYNDROME PLCB1 23236 phospholipase C beta 1 Q9NQ66
C1868684 EAR, PATELLA, SHORT STATURE SYNDROME ACHE 43 acetylcholinesterase (Cartwright blood group) P22303
C1868684 EAR, PATELLA, SHORT STATURE SYNDROME CLEC7A 64581 C-type lectin domain containing 7A Q9BXN2
C1868684 EAR, PATELLA, SHORT STATURE SYNDROME PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C1868684 EAR, PATELLA, SHORT STATURE SYNDROME PLA2G4A 5321 phospholipase A2 group IVA P47712

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