Gene

spata7

ID
ZDB-GENE-050419-61
Name
spermatogenesis associated 7
Symbol
spata7 Nomenclature History
Previous Names
  • si:ch211-51o12.1
Type
protein_coding_gene
Location
Chr: 17 Mapping Details/Browsers
Description
Human ortholog(s) of this gene implicated in Leber congenital amaurosis 3. Orthologous to human SPATA7 (spermatogenesis associated 7).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With spata7 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Leber congenital amaurosis 3 Alliance Leber congenital amaurosis 3 604232
Leber congenital amaurosis 3 Alliance Retinitis pigmentosa 94, variable age at onset, autosomal recessive 604232
Associated With spata7 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR029357 Spermatogenesis-associated protein 7
Domain Details Per Protein
Protein Length Spermatogenesis-associated protein 7
UniProtKB:F1QIV7 493
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA spata7-201 (1) Havana 1937 nt
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations