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
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Qin et al., 2022
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
5 figures from Qin et al., 2022
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With nobox Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
primary ovarian insufficiency 5 Alliance Premature ovarian failure 5 611548
Associated With nobox Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Transcripts
Genome Browsers
No data available
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations