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 57751 - 57775 of 62743 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
C1839839 MAJOR AFFECTIVE DISORDER 2 PLB1 151056 phospholipase B1 Q6P1J6
C1839839 MAJOR AFFECTIVE DISORDER 2 DGKH 160851 diacylglycerol kinase eta Q86XP1
C1839839 MAJOR AFFECTIVE DISORDER 2 ACE 1636 angiotensin I converting enzyme P12821
C1839839 MAJOR AFFECTIVE DISORDER 2 GAD1 2571 glutamate decarboxylase 1 Q99259
C1839839 MAJOR AFFECTIVE DISORDER 2 IMPA2 3613 inositol monophosphatase 2 O14732
C1839839 MAJOR AFFECTIVE DISORDER 2 NCAM1 4684 neural cell adhesion molecule 1 P13591
C1839839 MAJOR AFFECTIVE DISORDER 2 PLA2G2A 5320 phospholipase A2 group IIA P14555
C1839839 MAJOR AFFECTIVE DISORDER 2 PLA2G10 8399 phospholipase A2 group X O15496
C1839839 MAJOR AFFECTIVE DISORDER 2 NPL 80896 N-acetylneuraminate pyruvate lyase Q9BXD5
C1839839 MAJOR AFFECTIVE DISORDER 2 PLA2G6 8398 phospholipase A2 group VI O60733
C1839839 MAJOR AFFECTIVE DISORDER 2 PLA2G4A 5321 phospholipase A2 group IVA P47712
C1839839 MAJOR AFFECTIVE DISORDER 2 INPP1 3628 inositol polyphosphate-1-phosphatase P49441
C1839839 MAJOR AFFECTIVE DISORDER 2 PIP4K2A 5305 phosphatidylinositol-5-phosphate 4-kinase type 2 alpha P48426
C1839839 MAJOR AFFECTIVE DISORDER 2 PLA2G1B 5319 phospholipase A2 group IB P04054
C1839840 MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE AKR1C4 1109 aldo-keto reductase family 1 member C4 P17516
C1839840 MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C1840061 SMALL PATELLA SYNDROME PLA2G2A 5320 phospholipase A2 group IIA P14555
C1840061 SMALL PATELLA SYNDROME PLA2G6 8398 phospholipase A2 group VI O60733
C1840061 SMALL PATELLA SYNDROME GAD2 2572 glutamate decarboxylase 2 Q05329
C1840061 SMALL PATELLA SYNDROME PLA2G1B 5319 phospholipase A2 group IB P04054
C1840235 SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR GAS1 2619 growth arrest specific 1 P54826
C1840322 ODONTOHYPOPHOSPHATASIA (disorder) ALPL 249 alkaline phosphatase, biomineralization associated P05186
C1840333 Barakat syndrome PARP1 142 poly(ADP-ribose) polymerase 1 P09874
C1840333 Barakat syndrome STS 412 steroid sulfatase P08842
C1840333 Barakat syndrome DGCR2 9993 DiGeorge syndrome critical region gene 2 P98153

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