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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 12826 - 12850 of 62743 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Gene Name UniProt ID
C0014869 Peptic Esophagitis PIK3CB 5291 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta P42338
C0014869 Peptic Esophagitis PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C0014869 Peptic Esophagitis PTGS2 5743 prostaglandin-endoperoxide synthase 2 P35354
C0268162 Pentosuria DCXR 51181 dicarbonyl and L-xylulose reductase Q7Z4W1
C0853105 Penis carcinoma SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0853105 Penis carcinoma MRC1 4360 mannose receptor C-type 1 P22897
C0853105 Penis carcinoma PIK3CD 5293 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta O00329
C0853105 Penis carcinoma PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C0853105 Penis carcinoma PIK3CB 5291 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta P42338
C0853105 Penis carcinoma PIK3CG 5294 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma P48736
C0030849 Penile Neoplasms PIK3CA 5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha P42336
C0030846 Penile Diseases INPP5E 56623 inositol polyphosphate-5-phosphatase E Q9NRR6
C0271829 Pendred's syndrome SLC26A2 1836 solute carrier family 26 member 2 P50443
C0271829 Pendred's syndrome ALDH7A1 501 aldehyde dehydrogenase 7 family member A1 P49419
C0271829 Pendred's syndrome PTGDS 5730 prostaglandin D2 synthase P41222
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
C0030809 Pemphigus Vulgaris MRC1 4360 mannose receptor C-type 1 P22897
C0030809 Pemphigus Vulgaris CYP21A2 1589 cytochrome P450 family 21 subfamily A member 2 P08686
C0263313 Pemphigus Foliaceus CD1D 912 CD1d molecule P15813
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Last updated: August 19, 2024