Gene
hmgb3b
- ID
- ZDB-GENE-050417-290
- Name
- high mobility group box 3b
- Symbol
- hmgb3b Nomenclature History
- Previous Names
-
- fa19b06
- fj43d02
- wu:fa19b06
- wu:fj43d02
- zgc:112073
- Type
- protein_coding_gene
- Location
- Chr: 21 Mapping Details/Browsers
- Description
- Predicted to enable DNA binding activity. Predicted to be located in chromosome and nucleus. Is expressed in central nervous system; intermediate cell mass of mesoderm; ovary; pectoral fin bud; and telencephalon. Human ortholog(s) of this gene implicated in syndromic microphthalmia 13. Orthologous to human HMGB3 (high mobility group box 3).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 5 figures from 4 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- IMAGE:6909793 (1 image)
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 |
---|---|---|---|
syndromic microphthalmia 13 | Alliance | ?Microphthalmia, syndromic 13 | 300915 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | High mobility group box domain | High mobility group box domain superfamily | High Mobility Group Box (HMGB) | HMG box A DNA-binding domain, conserved site |
---|---|---|---|---|---|
UniProtKB:Q567G0
|
198 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
hmgb3b-201
(1)
|
Ensembl | 1,410 nt | ||
mRNA |
hmgb3b-202
(1)
|
Ensembl | 794 nt | ||
mRNA |
hmgb3b-203
(1)
|
Ensembl | 604 nt |
Interactions and Pathways
No data available
Plasmids
No data available