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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
GDNF family receptor alpha 1
Summary
- Gene Symbol
-
- GFRA1
- Aliases
-
- GDNFR
- GFR-ALPHA-1
- RET1L
- RETL1
- TRNR1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Disease variant
- Disulfide bond
- Endosome
- GPI-anchor
- Glycoprotein
- Golgi apparatus
- Receptor
- Reference proteome
- Repeat
- Signal
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| male gonad development | ||
| kidney development | ||
| neuron projection development | ||
| cell surface receptor signaling pathway |
|
GO Hierarchy
biological process
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
positive regulation of biological process [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| receptor complex | ||
| extrinsic component of membrane |
|
|
| external side of plasma membrane | ||
| axon | ||
| neuronal cell body |
| GO Term | Evidence Code | PMID |
|---|---|---|
| glial cell-derived neurotrophic factor receptor activity | ||
| neurotrophin receptor activity | ||
| integrin binding | ||
| signaling receptor binding |
|
|
| signaling receptor activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060161 | Kennedy's disease | |
| DOID:0060193 | amyotrophic lateral sclerosis type 1 | |
| DOID:0060194 | amyotrophic lateral sclerosis type 2 | |
| DOID:0060196 | amyotrophic lateral sclerosis type 4 | |
| DOID:0060250 | idiopathic scoliosis | |
| DOID:0060318 | acute promyelocytic leukemia | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0080348 | Alzheimer's disease 1 | |
| DOID:0080855 | Parkinsonism | |
| DOID:0110035 | Alzheimer's disease 2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001958 | Nonketotic hypoglycemia |
| HP:0002009 | Potter facies |
| HP:0002089 | Pulmonary hypoplasia |
| HP:0002242 | Abnormal intestine morphology |
| HP:0002575 | Tracheoesophageal fistula |
| HP:0002878 | Respiratory failure |
| HP:0003577 | Congenital onset |
| HP:0005107 | Abnormal sacrum morphology |
| HP:0010497 | Sirenomelia |
| HP:0010958 | Bilateral renal agenesis |
| Disease ID | Disease Name |
|---|---|
| ORPHA:1848 |
|
| OMIM:619887 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 103188960 | CALMI40351 | ||
| 79376 | ZFIN:ZDB-GENE-010226-2 | ||
| 79377 | ZFIN:ZDB-GENE-010226-3 | ||
| 108696016 | Xenbase:XB-GENE-6487060 | ||
| 108697312 | Xenbase:XB-GENE-17343984 | ||
| 100125202 | Xenbase:XB-GENE-1013855 | ||
| 109324042 | CROPO14511 | ||
| 101801788 | ANAPL04350 | ||
| 103813808 | SERCA07449 | ||
| 100083375 | ORNAN07377 |
