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 |
---|---|---|---|---|---|
C0014175 | Endometriosis | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0917713 | Becker Muscular Dystrophy | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0024305 | Lymphoma, Non-Hodgkin | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0036631 | Seminoma | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0585442 | Osteosarcoma of bone | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C3250443 | MYOTONIC DYSTROPHY 1 | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0021390 | Inflammatory Bowel Diseases | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0015230 | Exanthema | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0005859 | Bloom Syndrome | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0017601 | Glaucoma | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0035412 | Rhabdomyosarcoma | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C1332979 | Childhood Lymphoma | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0018021 | Goiter | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0039538 | Teratoma | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0023473 | Myeloid Leukemia, Chronic | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0024623 | Malignant neoplasm of stomach | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0020473 | Hyperlipidemia | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0751494 | Convulsive Seizures | ALPL | 249 | alkaline phosphatase, biomineralization associated | P05186 |
C0220743 | Childhood hypophosphatasia (disorder) | ALPL | 249 | alkaline phosphatase, biomineralization associated | P05186 |
C0020630 | Hypophosphatasia | ALPL | 249 | alkaline phosphatase, biomineralization associated | P05186 |
C0520739 | Hereditary pyropoikilocytosis | ALPL | 249 | alkaline phosphatase, biomineralization associated | P05186 |
C0001787 | Osteoporosis, Age-Related | ALPL | 249 | alkaline phosphatase, biomineralization associated | P05186 |
C0268413 | Adult hypophosphatasia (disorder) | ALPL | 249 | alkaline phosphatase, biomineralization associated | P05186 |
C0004153 | Atherosclerosis | ALPL | 249 | alkaline phosphatase, biomineralization associated | P05186 |
C0268412 | Infantile hypophosphatasia | ALPL | 249 | alkaline phosphatase, biomineralization associated | P05186 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024