GO Term | Evidence Code | PMID |
---|---|---|
regulation of meiotic nuclear division | ||
intracellular calcium ion homeostasis |
|
|
response to xenobiotic stimulus | ||
cellular response to electrical stimulus | ||
regulation of transcription, DNA-templated |
|
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 |
---|---|---|
hormone binding | ||
ubiquitin protein ligase binding | ||
iron ion binding | ||
protein-folding chaperone binding |
|
|
complement component C1q complex binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060678 | catecholaminergic polymorphic ventricular tachycardia 4 | |
DOID:0060679 | catecholaminergic polymorphic ventricular tachycardia 5 | |
DOID:0060777 | congenital secretory sodium diarrhea 8 | |
DOID:0060781 | congenital secretory sodium diarrhea 3 | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0070094 | oculocutaneous albinism type IA | |
DOID:0070113 | Niemann-Pick disease type C1 | |
DOID:0080070 | mucolipidosis II alpha/beta |
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 |
---|---|---|---|
117038294 | RHIFE15880 | ||
100190479 | TAEGU19745 | ||
103234003 | CHLSB15354 | ||
108544097 | RHIBE36442 | ||
104661079 | RHIRO03212 | ||
100601669 | NOMLE00120 | ||
114587853 | PODMU24721 | ||
107548191 | SINGR03195 | ||
107548256 | SINGR03195 | ||
106844337 | EQUAS28931 |
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