Species: Hu, Ca
Applications: WB, ELISA, ICC/IF
Host: Mouse Monoclonal
Species: Mu, Rt
Applications: WB, ELISA
Host: Rabbit Polyclonal
Species: Hu, Mu, Rt
Applications: IHC
Host: Rabbit Polyclonal
Species: Hu
Applications: WB
Species: Hu
Applications: WB, ELISA, MA, AP
Species: Hu
Applications: AC
Description
BBS2 encodes a protein of unknown function. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 2. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. [provided by RefSeq]
Bioinformatics
| Entrez |
Human
|
| Uniprot |
Human
Human
|
| Product By Gene ID |
583 |
| Alternate Names |
- Bardet-Biedl syndrome 2 protein
- Bardet-Biedl syndrome 2
- BBS
- MGC20703
|
Research Areas for BBS2
Find related products by research area and learn more about each of the different research areas below.
Vision
