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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 |
|---|---|---|
| heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules |
|
|
| positive regulation of dendritic spine morphogenesis | ||
| negative regulation of exocytosis | ||
| positive regulation of synapse assembly | ||
| neuron differentiation |
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:0050745 | diffuse large B-cell lymphoma | |
| DOID:0050776 | non-syndromic X-linked intellectual disability | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060427 | chromosome Xp21 deletion syndrome | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0080156 | X-linked adrenal hypoplasia congenita | |
| DOID:0112022 | non-syndromic X-linked intellectual disability 21 | |
| DOID:1059 | intellectual disability | |
| DOID:1094 | attention deficit hyperactivity disorder | |
| DOID:114 | heart disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001250 | Seizure |
| HP:0001382 | Joint hypermobility |
| HP:0001419 | X-linked recessive inheritance |
| HP:0001611 | Hypernasal speech |
| HP:0002342 | Intellectual disability, moderate |
| HP:0003196 | Short nose |
| HP:0009909 | Uplifted earlobe |
| HP:0010804 | Tented upper lip vermilion |
| HP:0100710 | Impulsivity |
| Disease ID | Disease Name |
|---|---|
| OMIM:300143 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 557801 | ZFIN:ZDB-GENE-090109-2 | ||
| 568868 | ZFIN:ZDB-GENE-061013-249 | ||
| 113578255 | ELEEL21072 | ||
| 106575569 | SALSA50103 | ||
| 115179295 | SALTR06579 | ||
| 115196347 | SALTR95378 | ||
| 100693228 | ORENI45011 | ||
| 115577155 | SPAAU66700 | ||
| 108707447 | Xenbase:XB-GENE-17338933 | ||
| 108708842 | Xenbase:XB-GENE-17338934 |
