Gene

fkbp10b

ID
ZDB-GENE-030131-3101
Name
FKBP prolyl isomerase 10b
Symbol
fkbp10b Nomenclature History
Previous Names
  • fkbp10
  • wu:fc27c03
Type
protein_coding_gene
Location
Chr: 12 Mapping Details/Browsers
Description
Predicted to have calcium ion binding activity and peptidyl-prolyl cis-trans isomerase activity. Is expressed in several structures, including ball; ectoderm; median fin fold; splanchnocranium; and vasculature. Human ortholog(s) of this gene implicated in osteogenesis imperfecta type 11. Orthologous to human FKBP10 (FKBP prolyl isomerase 10).
Genome Resources
Note
None
Expression
All Expression Data
13 figures from 2 publications
Cross-Species Comparison
High Throughput Data
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 fkbp10b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Bruck syndrome Alliance Bruck syndrome 1 259450
osteogenesis imperfecta type 11 Alliance Osteogenesis imperfecta, type XI 610968
Associated With fkbp10b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Binding_site IPR018247 EF-Hand 1, calcium-binding site
Domain IPR001179 FKBP-type peptidyl-prolyl cis-trans isomerase domain
Domain IPR002048 EF-hand domain
Homologous_superfamily IPR011992 EF-hand domain pair
Domain Details Per Protein
Protein Length EF-Hand 1, calcium-binding site EF-hand domain EF-hand domain pair FKBP-type peptidyl-prolyl cis-trans isomerase domain
UniProtKB:R4GDZ4 197
UniProtKB:B3DKC0 614
UniProtKB:Q7ZVA7 614
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Ensembl Gene Tree
Citations