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
- Acts upstream of or within cerebellar granule cell differentiation and neuron migration. 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