MICAL2: Microtubule Associated Monooxygenase, Calponin And LIM Domain Containing 2

A key regulator of actin dynamics, cell migration, and neuronal development, implicated in cancer and neurological disorders.

Gene Information Card

Symbol MICAL2
Full Name Microtubule Associated Monooxygenase, Calponin And LIM Domain Containing 2
Gene Type Protein coding
Chromosomal Location 11p15.3
NCBI Gene ID 9645 ncbi.nlm.nih.gov/gene/9645
Ensembl ID ENSG00000148848
UniProt ID O94851
OMIM ID 608887
HGNC ID 24694
Aliases MICAL-2, MICAL2A, MICAL2B, FLJ10154

Description

MICAL2 is a multidomain protein that acts as a flavoprotein monooxygenase, regulating actin cytoskeleton dynamics through redox-dependent mechanisms. It is involved in semaphorin signaling, cell migration, axon guidance, and neuronal development. MICAL2 is overexpressed in various cancers and contributes to tumor progression and metastasis.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (multiple types) Overexpression of MICAL2 promotes cell migration, invasion, and metastasis via actin depolymerization and activation of signaling pathways (e.g., Rac1). COSMIC, NCBI Gene, PubMed
Neurodevelopmental disorders MICAL2 is involved in axon guidance and neuronal migration; dysregulation may contribute to intellectual disability and autism spectrum disorders. OMIM, NCBI Gene
Cardiovascular disease MICAL2 regulates endothelial cell migration and angiogenesis; altered expression may affect vascular remodeling. UniProt, PubMed

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 15.2 Medium
Lung 8.7 Low
Heart 6.3 Low
Liver 4.1 Not detected
Kidney 9.5 Low
Testis 20.1 High
Cell Line Expression
Cell Line nTPM Notes
HeLa 12.4 Cervical cancer cell line
A549 18.7 Lung adenocarcinoma cell line
MCF7 9.8 Breast cancer cell line
SH-SY5Y 22.3 Neuroblastoma cell line
HEK293 7.5 Embryonic kidney cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1234C>T (p.Arg412Cys) Missense 0.02% (gnomAD) Unknown; predicted damaging by SIFT/PolyPhen
c.567_568insA (p.Glu190fs) Frameshift Rare Loss of function; truncation of protein
c.2345G>A (p.Gly782Asp) Missense 0.01% (gnomAD) Unknown; located in LIM domain, may affect protein interactions
Mutation functional classification

Loss of Function (LOF)

Frameshift and nonsense mutations that truncate the protein, leading to loss of monooxygenase activity and actin-regulatory function.

Gain of Function (GOF)

Missense mutations in the catalytic domain that enhance enzyme activity or alter substrate specificity, potentially promoting cell migration.

Dominant Negative (DN)

Mutations in the calponin homology domain that disrupt actin binding but retain dimerization, interfering with wild-type MICAL2 function.

Pathways

Semaphorin signaling pathway (Reactome: R-HSA-373755)
Rac1 signaling pathway (Reactome: R-HSA-9013408)
Actin cytoskeleton regulation (Reactome: R-HSA-5663205)

Protein Summary

MICAL2 is a 1118-amino acid protein containing a flavin adenine dinucleotide (FAD)-binding monooxygenase domain, a calponin homology (CH) domain, a LIM domain, and a coiled-coil region. It catalyzes the oxidation of actin methionine residues, leading to actin filament disassembly. MICAL2 also interacts with semaphorin receptors and regulates Rac1 activity, influencing cell morphology and migration. Its expression is enriched in the brain and testis, and it is upregulated in multiple cancers.

Related Products

Product name Cat.No. Species Gene ID
MICAL2 Knockout HEK293 Cell Line EDJ-KQ6681 Human 9645 Details Get a Quote
MICAL2 Knockout A-549 Cell Line EDJ-KQ31014 Human 9645 Details Get a Quote
MICAL2 Knockout HCT 116 Cell Line EDJ-KQ31015 Human 9645 Details Get a Quote
MICAL2 Knockout HeLa Cell Line EDJ-KQ31016 Human 9645 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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