GO Term | Evidence Code | PMID |
---|---|---|
response to estradiol | ||
peptide antigen assembly with MHC class I protein complex |
GO Term | Evidence Code | PMID |
---|---|---|
nucleus | ||
nuclear envelope | ||
endoplasmic reticulum lumen | ||
MHC class I peptide loading complex | ||
endoplasmic reticulum-Golgi intermediate compartment membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
DNA binding |
|
|
integrin binding | ||
zinc ion binding |
|
|
nuclear androgen receptor binding | ||
protein folding chaperone |
|
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:898 | autosomal dominant polycystic kidney disease | |
DOID:8991 | cervix uteri carcinoma in situ | |
DOID:8997 | polycythemia vera | |
DOID:9074 | systemic lupus erythematosus | |
DOID:9119 | acute myeloid leukemia | |
DOID:9164 | achalasia | |
DOID:92 | speech disorder | |
DOID:9206 | Barrett's esophagus | |
DOID:9256 | colorectal cancer | |
DOID:9261 | nasopharynx carcinoma |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000505 | Visual impairment |
HP:0000952 | Jaundice |
HP:0000967 | Petechiae |
HP:0000978 | Bruising susceptibility |
HP:0000979 | Purpura |
HP:0000980 | Pallor |
HP:0001028 | Hemangioma |
HP:0001082 | Cholecystitis |
HP:0001394 | Cirrhosis |
Disease ID | Disease Name |
---|---|
ORPHA:824 |
|
OMIM:254450 |
|
ORPHA:3318 |
|
OMIM:187950 |
|
ORPHA:131 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101676085 | MUSPF15170 | ||
101087384 | FELCA03901 | ||
122214022 | PANLE23019 | ||
101334581 | TURTR03914 | ||
118892014 | BALMU07452 | ||
100653854 | LOXAF11718 | ||
100064107 | HORSE38134 | ||
100381266 | PIGXX18295 | ||
281036 | BOVIN32488 | ||
102185733 | CAPHI28298 |
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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