Gene

setbp1

ID
ZDB-GENE-060526-72
Name
SET binding protein 1
Symbol
setbp1 Nomenclature History
Previous Names
  • si:ch211-198e13.1
Type
protein_coding_gene
Location
Chr: 5 Mapping Details/Browsers
Description
Predicted to enable DNA binding activity. Human ortholog(s) of this gene implicated in autosomal dominant non-syndromic intellectual disability 29. Orthologous to human SETBP1 (SET binding protein 1).
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 setbp1 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal dominant non-syndromic intellectual disability 29 Alliance Mental retardation, autosomal dominant 29 616078
Schinzel-Giedion midface retraction syndrome 269150
Associated With setbp1 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Conserved_site IPR017956 AT hook, DNA-binding motif
Domain Details Per Protein
Protein Length AT hook, DNA-binding motif
UniProtKB:B0R147 1438
Transcripts
Genome Browsers
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