GO Term | Evidence Code | PMID |
---|---|---|
regulation of heart rate by cardiac conduction | ||
calcium ion transport | ||
regulation of ventricular cardiac muscle cell membrane repolarization | ||
cellular response to amyloid-beta | ||
calcium ion import across plasma membrane |
GO Term | Evidence Code | PMID |
---|---|---|
L-type voltage-gated calcium channel complex | ||
neuronal dense core vesicle | ||
voltage-gated calcium channel complex | ||
plasma membrane | ||
sarcoplasmic reticulum |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050451 | Brugada syndrome | |
DOID:0050562 | West syndrome | |
DOID:0050793 | short QT syndrome | |
DOID:0050820 | atrioventricular block | |
DOID:0060224 | atrial fibrillation | |
DOID:0060250 | idiopathic scoliosis | |
DOID:0060319 | cardiac arrest | |
DOID:0070395 | developmental and epileptic encephalopathy 110 | |
DOID:0110066 | amelogenesis imperfecta type 1G | |
DOID:0110218 | Brugada syndrome 1 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000218 | High palate |
HP:0000252 | Microcephaly |
HP:0000341 | Narrow forehead |
HP:0000348 | High forehead |
HP:0000369 | Low-set ears |
HP:0000400 | Macrotia |
HP:0000494 | Downslanted palpebral fissures |
HP:0000504 | Abnormality of vision |
HP:0000508 | Ptosis |
Disease ID | Disease Name |
---|---|
ORPHA:51083 |
|
OMIM:620149 |
|
ORPHA:442835 |
|
ORPHA:130 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
174730 | WB:WBGene00007041 | ||
176155 | WB:WBGene00006772 | ||
100186976 | CIOIN07698 | ||
561434 | ZFIN:ZDB-GENE-041210-215 | ||
106561208 | SALSA52251 | ||
113026874 | ASTCA38473 | ||
108711204 | Xenbase:XB-GENE-6488701 | ||
108713061 | Xenbase:XB-GENE-17341694 | ||
100036724 | Xenbase:XB-GENE-964524 | ||
101946496 | CHRPI00363 |
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
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: August 19, 2024