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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 |
| Disease ID | Disease Name ▲ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C1263846 | Attention deficit hyperactivity disorder | CDH13 | 1012 | cadherin 13 | P55290 |
| C1263846 | Attention deficit hyperactivity disorder | CNTN1 | 1272 | contactin 1 | Q12860 |
| C1263846 | Attention deficit hyperactivity disorder | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
| C1263846 | Attention deficit hyperactivity disorder | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C1263846 | Attention deficit hyperactivity disorder | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| C1263846 | Attention deficit hyperactivity disorder | ARSD | 414 | arylsulfatase D | P51689 |
| C1263846 | Attention deficit hyperactivity disorder | CYP4F3 | 4051 | cytochrome P450 family 4 subfamily F member 3 | Q08477 |
| C1263846 | Attention deficit hyperactivity disorder | OCRL | 4952 | OCRL inositol polyphosphate-5-phosphatase | Q01968 |
| C1263846 | Attention deficit hyperactivity disorder | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C1263846 | Attention deficit hyperactivity disorder | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C1263846 | Attention deficit hyperactivity disorder | PRNP | 5621 | prion protein | F7VJQ1 |
| C1263846 | Attention deficit hyperactivity disorder | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C1263846 | Attention deficit hyperactivity disorder | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C1263846 | Attention deficit hyperactivity disorder | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C2931788 | Atypical Hemolytic Uremic Syndrome | PIGA | 5277 | phosphatidylinositol glycan anchor biosynthesis class A | P37287 |
| C2931788 | Atypical Hemolytic Uremic Syndrome | G6PD | 2539 | glucose-6-phosphate dehydrogenase | P11413 |
| C2931788 | Atypical Hemolytic Uremic Syndrome | GPI | 2821 | glucose-6-phosphate isomerase | P06744 |
| C2931788 | Atypical Hemolytic Uremic Syndrome | GRHPR | 9380 | glyoxylate and hydroxypyruvate reductase | Q9UBQ7 |
| C2931788 | Atypical Hemolytic Uremic Syndrome | MASP1 | 5648 | mannan binding lectin serine peptidase 1 | P48740 |
| C2931788 | Atypical Hemolytic Uremic Syndrome | BAAT | 570 | bile acid-CoA:amino acid N-acyltransferase | Q14032 |
| C2931788 | Atypical Hemolytic Uremic Syndrome | DGKE | 8526 | diacylglycerol kinase epsilon | P52429 |
| C0751776 | Atypical Inclusion-Body Disease | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0751776 | Atypical Inclusion-Body Disease | EPM2A | 7957 | EPM2A glucan phosphatase, laforin | O95278 |
| C0751776 | Atypical Inclusion-Body Disease | PRNP | 5621 | prion protein | P04156 |
| C0751776 | Atypical Inclusion-Body Disease | CERS1 | 10715 | ceramide synthase 1 | P27544 |
