Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
interleukin 1 receptor accessory protein like 1
Summary
- Gene Symbol
-
- IL1RAPL1
- Aliases
-
- IL1R8
- OPHN4
- TIGIRR-2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Cell projection
- Cytoplasm
- Disulfide bond
- Glycoprotein
- Hydrolase
- Immunoglobulin domain
- Intellectual disability
- NAD
- Receptor
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| signal transduction | ||
| trans-synaptic signaling by trans-synaptic complex | ||
| regulation of postsynapse organization |
GO Hierarchy
biological process
biological regulation [inference]
regulation of biological process [inference]
positive regulation of biological process [inference]
regulation of developmental process [inference]
regulation of cellular process [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| NAD+ nucleosidase activity | ||
| NAD+ nucleotidase, cyclic ADP-ribose generating | ||
| signaling receptor binding | ||
| interleukin-1 binding | ||
| protein binding |
GO Hierarchy
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:13934 | facial paralysis | |
| DOID:14323 | Marfan syndrome | |
| DOID:1612 | breast cancer | |
| DOID:162 | cancer | |
| DOID:1756 | facial nerve disease | |
| DOID:1909 | melanoma | |
| DOID:1921 | Klinefelter syndrome | |
| DOID:2841 | asthma | |
| DOID:2914 | immune system disease | |
| DOID:3459 | breast carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000053 | Macroorchidism |
| HP:0000194 | Open mouth |
| HP:0000303 | Mandibular prognathia |
| HP:0000316 | Hypertelorism |
| HP:0000486 | Strabismus |
| HP:0000582 | Upslanted palpebral fissure |
| HP:0000664 | Synophrys |
| HP:0000678 | Dental crowding |
| HP:0000717 | Autism |
| HP:0000752 | Hyperactivity |
| Disease ID | Disease Name |
|---|---|
| OMIM:300143 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101561386 | OCTDE08057 | ||
| 101706420 | HETGA14233 | ||
| 101873084 | MELUD02999 | ||
| 102448231 | PELSI15515 | ||
| 102526558 | VICPA00767 | ||
| 105867139 | MICMU14026 | ||
| 101068376 | TAKRU48017 | ||
| 105714753 | AOTNA13656 | ||
| 101033234 | SAIBB07063 | ||
| 101609103 | JACJA15276 |
