Target intelligence / Profile preview

C-Maf inducing protein (CMIP)

Target
CMIP
Molecular classification
Other (Adaptor protein)
01

Overview

C-Maf inducing protein (CMIP) is a multifunctional adaptor protein encoded by the CMIP gene on chromosome 16q24[1][3]. It contains domains such as a pleckstrin homology (PH) domain, leucine-rich repeats, and SH3 domain, which support diverse protein interactions. CMIP plays critical roles in T cell signaling and regulation, podocyte cytoskeletal organization in the kidney, and neurodevelopment[1][2][3]. In the immune system, CMIP can inhibit activation and proliferation of T cells and biases cytokine responses. In kidney podocytes, it disrupts cytoskeletal and signaling complexes, contributing to glomerular diseases like minimal change nephrotic syndrome and focal segmental glomerulosclerosis[2]. Overexpression has also been linked to several cancers, where CMIP may promote tumor cell proliferation and migration by modulating pathways such as NF-κB and interaction with proteins like MDM2 and SOX2[1][2]. CMIP’s disease associations extend to neurodevelopmental and metabolic disorders. Because of its pivotal signaling functions and links to disease, CMIP is considered a possible therapeutic target, though no approved drugs or direct modulators are currently known[1][2][3].

Other names
C-Maf-inducing proteinKIAA1694TCMIPc-MipTc-MipTruncated c-Maf-inducing proteintc-MipCMIP
02

Biological functions

Signal transductionImmune responseCell survival and apoptosis regulationCytoskeletal organizationNeurodevelopment
03

Disease associations

CancerGlomerular diseases (e.g., minimal change nephrotic syndrome, focal segmental glomerulosclerosis)Neurodevelopmental disease (e.g., dyslexia, language impairment)Metabolic disease
04

Safety considerations

Renal toxicity (esp. nephrotic syndrome), particularly as an adverse event in anti-receptor tyrosine kinase anticancer therapy[1]Impact on immune system regulation
05

Biomarkers

Overexpression in podocytes for nephrotic syndromeOverexpression in tumor cell populations (research context)

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