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EXPH5 Geneexophilin 5 The protein encoded by this gene is a member of the synaptotagmin-like protein (Slp) family lacking a C2 domain. It contains an N-terminal synaptotagmin-like homology domain (SHD), and is a ras-related protein Rab-27B effector protein. This protein is thought to be involved in exosome secretion and intracellular vesicle trafficking. Reduced expression of this gene results in keratin filament defects. Mutations in this gene have been associated with some cases of epidermolysis bullosa, an inherited skin fragility disorder. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015] |
EXPH5 Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for EXPH5 from the Pathway Commons Protein-Protein Interactions dataset. |
Human - Motor Cortex - Cluster - VIP+ EXPH5+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ EXPH5+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Brain_CT2_Inh L1-2 VIP EXPH5 Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Brain_CT2_Inh L1-2 VIP EXPH5 cell type from the HuBMAP ASCT+B dataset. |
Brain_CT2_Inh L1-2 VIP EXPH5 Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Brain_CT2_Inh L1-2 VIP EXPH5 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |