RIMBP2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

RIMS binding protein 2 is a protein that in humans is encoded by the RIMBP2 gene. [5] This protein plays a significant role in synaptic transmission and is involved in the regulation of voltage-gated calcium channels, which are crucial for neurotransmitter release at synapses.[6][7]

PDBOrtholog search: PDBe RCSB
AliasesRIMBP2, PPP1R133, RBP2, RIM-BP2, RIMS binding protein 2
Quick facts Available structures, PDB ...
RIMBP2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRIMBP2, PPP1R133, RBP2, RIM-BP2, RIMS binding protein 2
External IDsOMIM: 611602; MGI: 2443235; HomoloGene: 14672; GeneCards: RIMBP2; OMA:RIMBP2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001081388
NM_001310733
NM_001378900

RefSeq (protein)

NP_001074857
NP_001297662
NP_001365829

Location (UCSC)Chr 12: 130.4 – 130.72 MbChr 5: 128.83 – 129.03 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Close

Function and characteristics

RIMBP2 is primarily located in the presynaptic active zones of neurons, where it contributes to the organization and maintenance of synaptic structures. It is essential for the proper functioning of synaptic vesicles and calcium-dependent processes that facilitate communication between neurons.[8][9]

Clinical relevance

Research has indicated that mutations or dysregulation of RIMBP2 may be associated with various neurological disorders, such as Pitt-Hopkins syndrome.[6][10]

References

Related Articles

Wikiwand AI