Gene
fkbp1b
- ID
- ZDB-GENE-040426-1785
- Name
- FKBP prolyl isomerase 1B
- Symbol
- fkbp1b Nomenclature History
- Previous Names
-
- si:dkeyp-115a10.1
- zgc:73381 (1)
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Predicted to have peptidyl-prolyl cis-trans isomerase activity. Predicted to be involved in chaperone-mediated protein folding and protein peptidyl-prolyl isomerization. Predicted to localize to cytoplasm. Human ortholog(s) of this gene implicated in Graves' disease. Is expressed in basal plate midbrain region; brain; cranial ganglion; and myotome. Orthologous to several human genes including FKBP1B (FKBP prolyl isomerase 1B).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- 5 figures from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:73381 (8 images)
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | FKBP-type Peptidyl-prolyl cis-trans Isomerase | FKBP-type peptidyl-prolyl cis-trans isomerase domain | Peptidyl-prolyl cis-trans isomerase domain superfamily |
---|---|---|---|---|
UniProtKB:Q6PBJ1
|
108 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
fkbp1b-201
(1)
|
Ensembl | 1,046 nt |
Interactions and Pathways
No data available
Plasmids
No data available