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 7151 - 7175 of 62743 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Gene Name UniProt ID
C1456781 Benign melanocytic nevus GALK1 2584 galactokinase 1 P51570
C1456781 Benign melanocytic nevus GPC3 2719 glypican 3 P51654
C1456781 Benign melanocytic nevus MTAP 4507 methylthioadenosine phosphorylase Q13126
C1456781 Benign melanocytic nevus NSDHL 50814 NAD(P) dependent steroid dehydrogenase-like Q15738
C1456781 Benign melanocytic nevus PKD1 5310 polycystin 1, transient receptor potential channel interacting P98161
C1456781 Benign melanocytic nevus PTEN 5728 phosphatase and tensin homolog P60484
C0496899 Benign neoplasm of brain, unspecified CYP2C9 1559 cytochrome P450 family 2 subfamily C member 9 P11712
C0496899 Benign neoplasm of brain, unspecified PTEN 5728 phosphatase and tensin homolog P60484
C0004991 Benign neoplasm of colon CEACAM5 1048 CEA cell adhesion molecule 5 P06731
C0496892 Benign neoplasm of kidney OGG1 4968 8-oxoguanine DNA glycosylase O15527
C0347272 Benign neoplasm of large intestine CEMIP 57214 cell migration inducing hyaluronidase 1 Q8WUJ3
C0496870 Benign neoplasm of liver ICAM1 3383 intercellular adhesion molecule 1 P05362
C0496870 Benign neoplasm of liver CYP3A4 1576 cytochrome P450 family 3 subfamily A member 4 P08684
C0684354 Benign neoplasm of sweat gland CEACAM5 1048 CEA cell adhesion molecule 5 P06731
C0005001 Benign prostatic hypertrophy SRD5A2 6716 steroid 5 alpha-reductase 2 P31213
C0149841 Benign recurrent intrahepatic cholestasis GGT1 2678 gamma-glutamyltransferase 1 P19440
C0005122 Beriberi CHAT 1103 choline O-acetyltransferase P28329
C0005122 Beriberi SLC35F3 148641 solute carrier family 35 member F3 Q8IY50
C0005122 Beriberi TKT 7086 transketolase P29401
C0005129 Bernard-Soulier Syndrome XYLT1 64131 xylosyltransferase 1 Q86Y38
C0005129 Bernard-Soulier Syndrome LGALS8 3964 galectin 8 O00214
C0005129 Bernard-Soulier Syndrome PRNP 5621 prion protein P04156
C0005129 Bernard-Soulier Syndrome PRNP 5621 prion protein F7VJQ1
C0005138 Berylliosis ACE 1636 angiotensin I converting enzyme P12821
C2350873 Beryllium Disease ACE 1636 angiotensin I converting enzyme P12821

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Last updated: August 19, 2024