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UNC13B

UNC13B
Identifiers
Aliases UNC13B, MUNC13, UNC13, Unc13h2, unc-13 homolog B (C. elegans)
External IDs MGI: 1342278 HomoloGene: 31376 GeneCards: UNC13B
Genetically Related Diseases
Parkinson's disease
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_006377
NM_001330653

NM_001081413
NM_021468
NM_001310758

RefSeq (protein)

NP_001317582
NP_006368

Location (UCSC) Chr 9: 35.16 – 35.41 Mb Chr 4: 43.06 – 43.26 Mb
PubMed search

NM_006377
NM_001330653

NM_001081413
NM_021468
NM_001310758

NP_001317582
NP_006368

NP_067443

Protein unc-13 homolog B is a protein that in humans is encoded by the UNC13B gene.

This gene is expressed in the kidney cortical epithelial cells and is upregulated by hyperglycemia. The encoded protein shares a high level of similarity to the rat homolog, and contains 3 C2 domains and a diacylglycerol-binding C1 domain. Hyperglycemia increases the levels of diacylglycerol, which has been shown to induce apoptosis in cells transfected with this gene and thus contribute to the renal cell complications of hyperglycemia. Studies in other species also indicate a role for this protein in the priming step of synaptic vesicle exocytosis.

UNC13B has been shown to interact with:


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Wikipedia

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