RIMBP2

RIMBP2
Identifiers
Aliases	RIMBP2, PPP1R133, RBP2, RIM-BP2, RIMS binding protein 2
External IDs	OMIM: 611602; MGI: 2443235; GeneCards: RIMBP2
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	1WIE, 2CSI, 2CSP, 2CSQ
Gene location (Human)
Chr.	Chromosome 12 (human)
End	130,716,281 bp
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)
End	129,030,550 bp
RNA expression pattern
	Top expressed in
	Brodmann area 10; ; frontal pole; ; pituitary gland; ; Region I of hippocampus proper; ; anterior pituitary; ; orbitofrontal cortex; ; Brodmann area 46; ; superior frontal gyrus; ; middle temporal gyrus; ; postcentral gyrus;
	Top expressed in
	visual cortex; ; primary visual cortex; ; dentate gyrus of hippocampal formation granule cell; ; superior frontal gyrus; ; superior cervical ganglion; ; islet of Langerhans; ; prefrontal cortex; ; piriform cortex; ; cingulate gyrus; ; primary motor cortex;
	More reference expression data
	n/a
Orthologs
Databases	NCBI: entry; OMA: entry
	23504
	231760
	ENSG00000060709
	ENSMUSG00000029420
	O15034
	Q80U40
NM_015347; NM_001351226; NM_001351227; NM_001351228; NM_001351229;
	NM_001351230; NM_001351231; NM_001351232; NM_001351233
	NM_001081388; NM_001310733; NM_001378900
NP_056162; NP_001338155; NP_001338156; NP_001338157; NP_001338158;
	NP_001338159; NP_001338160; NP_001338161; NP_001338162
	NP_001074857; NP_001297662; NP_001365829
	Wikidata
View/Edit Human	View/Edit Mouse

RIMS binding protein 2 is a protein that in humans is encoded by the RIMBP2 gene. 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.

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.

Clinical relevance

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

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000060709 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000029420 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Entrez Gene: RIMS binding protein 2". Retrieved 2016-02-11.
1 2 RGD. "Rimbp2 (RIMS binding protein 2) - Rat Genome Database". rgd.mcw.edu. Retrieved 2024-10-20.
↑ Mittelstaedt T, Schoch S (November 2007). "Structure and evolution of RIM-BP genes: identification of a novel family member". Gene. 403 (1–2): 70–79. doi:10.1016/j.gene.2007.08.004. PMID 17855024.
↑ "RIMBP2 protein expression summary - The Human Protein Atlas". www.proteinatlas.org. Retrieved 2024-10-20.
↑ Butola T, Alvanos T, Hintze A, Koppensteiner P, Kleindienst D, Shigemoto R, et al. (September 2021). "RIM-Binding Protein 2 Organizes Ca²⁺ Channel Topography and Regulates Release Probability and Vesicle Replenishment at a Fast Central Synapse". The Journal of Neuroscience. 41 (37): 7742–7767. doi:10.1523/JNEUROSCI.0586-21.2021. PMC 8445062. PMID 34353898.
↑ Davis BA, Chen HY, Ye Z, Ostlund I, Tippani M, Das D, et al. (April 2024). "TCF4 Mutations Disrupt Synaptic Function Through Dysregulation of RIMBP2 in Patient-Derived Cortical Neurons". Biological Psychiatry. 95 (7): 662–675. doi:10.1016/j.biopsych.2023.07.021. PMC 10858293. PMID 37573005.

External links

PDBe-KB provides an overview of all the structure information available in the PDB for Human RIMS-binding protein 2 (RIMBP2)

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000060709 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000029420 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "Entrez Gene: RIMS binding protein 2". Retrieved 2016-02-11.

[RGD-6] 1 2 RGD. "Rimbp2 (RIMS binding protein 2) - Rat Genome Database". rgd.mcw.edu. Retrieved 2024-10-20.

[7] Mittelstaedt T, Schoch S (November 2007). "Structure and evolution of RIM-BP genes: identification of a novel family member". Gene. 403 (1–2): 70–79. doi:10.1016/j.gene.2007.08.004. PMID 17855024.

[8] "RIMBP2 protein expression summary - The Human Protein Atlas". www.proteinatlas.org. Retrieved 2024-10-20.

[9] Butola T, Alvanos T, Hintze A, Koppensteiner P, Kleindienst D, Shigemoto R, et al. (September 2021). "RIM-Binding Protein 2 Organizes Ca²⁺ Channel Topography and Regulates Release Probability and Vesicle Replenishment at a Fast Central Synapse". The Journal of Neuroscience. 41 (37): 7742–7767. doi:10.1523/JNEUROSCI.0586-21.2021. PMC 8445062. PMID 34353898.

[10] Davis BA, Chen HY, Ye Z, Ostlund I, Tippani M, Das D, et al. (April 2024). "TCF4 Mutations Disrupt Synaptic Function Through Dysregulation of RIMBP2 in Patient-Derived Cortical Neurons". Biological Psychiatry. 95 (7): 662–675. doi:10.1016/j.biopsych.2023.07.021. PMC 10858293. PMID 37573005.