Gene
nobox
- ID
- ZDB-GENE-030131-6376
- Name
- NOBOX oogenesis homeobox
- Symbol
- nobox Nomenclature History
- Previous Names
-
- fi69e09
- wu:fi69e09
- Type
- protein_coding_gene
- Location
- Chr: 19 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in premature ovarian failure. Orthologous to human NOBOX (NOBOX oogenesis homeobox).
- Genome Resources
-
- Alliance (1)
- Gene:334444 (1)
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Qin et al., 2022
- Cross-Species Comparison
- High Throughput Data
-
- GEO (1) Expression Atlas (1) Single Cell Expression Atlas (1) Daniocell (1)
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 5 figures from Qin et al., 2022
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| primary ovarian insufficiency 5 | Alliance | Premature ovarian failure 5 | 611548 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Helix-turn-helix motif | Homedomain-like superfamily | Homeobox protein NOBOX | Homeodomain |
|---|---|---|---|---|---|
|
UniProtKB:A0A8M9PHQ5
|
235 | ||||
|
UniProtKB:A0A8M9PZH3
|
148 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance