Gene
hgfb
- ID
- ZDB-GENE-041014-3
- Name
- hepatocyte growth factor b
- Symbol
- hgfb Nomenclature History
- Previous Names
-
- hgf2
- Type
- protein_coding_gene
- Location
- Chr: 18 Mapping Details/Browsers
- Description
- Predicted to enable signaling receptor binding activity. Acts upstream of or within cerebellar granule cell differentiation and neuron migration. Predicted to be active in extracellular space. Is expressed in several structures, including hindbrain neural rod; nervous system; pancreatic system; presumptive rhombomere 1; and swim bladder bud. Human ortholog(s) of this gene implicated in several diseases, including artery disease (multiple); autosomal recessive nonsyndromic deafness 39; eye disease (multiple); neuropathy (multiple); and scleroderma (multiple). Orthologous to human HGF (hepatocyte growth factor).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 6 figures from 4 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| autosomal recessive nonsyndromic deafness 39 | Alliance | Deafness, autosomal recessive 39 | 608265 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
- Genome Browsers
Interactions and Pathways
Plasmids
No data available