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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name ▲ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0238461 | Anaplastic thyroid carcinoma | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0238461 | Anaplastic thyroid carcinoma | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0238461 | Anaplastic thyroid carcinoma | TKT | 7086 | transketolase | P29401 |
C0039585 | Androgen-Insensitivity Syndrome | CHI3L1 | 1116 | chitinase 3 like 1 | P36222 |
C0039585 | Androgen-Insensitivity Syndrome | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0039585 | Androgen-Insensitivity Syndrome | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
C0039585 | Androgen-Insensitivity Syndrome | GAD1 | 2571 | glutamate decarboxylase 1 | Q99259 |
C0039585 | Androgen-Insensitivity Syndrome | LGALS1 | 3956 | galectin 1 | P09382 |
C0039585 | Androgen-Insensitivity Syndrome | LGALS3 | 3958 | galectin 3 | P17931 |
C0039585 | Androgen-Insensitivity Syndrome | STS | 412 | steroid sulfatase | P08842 |
C0039585 | Androgen-Insensitivity Syndrome | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
C0039585 | Androgen-Insensitivity Syndrome | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0039585 | Androgen-Insensitivity Syndrome | AKR1C3 | 8644 | aldo-keto reductase family 1 member C3 | P42330 |
C0039585 | Androgen-Insensitivity Syndrome | CDH13 | 1012 | cadherin 13 | P55290 |
C0039585 | Androgen-Insensitivity Syndrome | GPX3 | 2878 | glutathione peroxidase 3 | P22352 |
C0039585 | Androgen-Insensitivity Syndrome | HSD17B7 | 51478 | hydroxysteroid 17-beta dehydrogenase 7 | P56937 |
C0039585 | Androgen-Insensitivity Syndrome | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
C0039585 | Androgen-Insensitivity Syndrome | SRD5A2 | 6716 | steroid 5 alpha-reductase 2 | P31213 |
C0162311 | Androgenetic Alopecia | AGA | 175 | aspartylglucosaminidase | P20933 |
C0162311 | Androgenetic Alopecia | PARP1 | 142 | poly(ADP-ribose) polymerase 1 | P09874 |
C0162311 | Androgenetic Alopecia | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0162311 | Androgenetic Alopecia | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
C0162311 | Androgenetic Alopecia | PRNP | 5621 | prion protein | P04156 |
C0162311 | Androgenetic Alopecia | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0162311 | Androgenetic Alopecia | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
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Last updated: August 19, 2024