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GeneQ18049313· pop 5· linked from 6 articles

Also known as CMG-2, CMG2, HFS, ISH, JHF, anthrax toxin receptor 2, ANTXR cell adhesion molecule 2

Anthrax toxin receptor 2 (also known as capillary morphogenesis gene 2 or CMG2) is a protein that in humans is encoded by the ANTXR2 gene.

Gene data

ANTXR2
Name
ANTXR cell adhesion molecule 2
Type
protein-coding
Aliases
CMG-2, CMG2, HFS, ISH, JHF

This gene encodes a receptor for anthrax toxin. The protein binds to collagen IV and laminin, suggesting that it may be involved in extracellular matrix adhesion. Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009].

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ANTXR cell adhesion molecule 2

Symbol
ANTXR2
Biotype
Protein coding
Organism
Homo sapiens
Location
4:79,901,146-80,125,454
Strand
Reverse (−)
Assembly
GRCh38
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via Ensembl · EMBL-EBI

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Encyclopedic overview

4 sections
Contents
  • See also
  • References
  • External links
  • Further reading

Anthrax toxin receptor 2 (also known as capillary morphogenesis gene 2 or CMG2) is a protein that in humans is encoded by the ANTXR2 gene.

Mutations in ANTXR2 are associated with infantile systemic hyalinosis and juvenile systemic hyalinosis, both autosomal recessive disorders. Biallelic missense mutations of ANTXR2 have been described in a case report of atypical infantile systemic hyalinosis with intestinal lymphangiectasia causing protein-losing enteropathy. Deuquet et al. (2009) found that three out of four missense mutations in the von Willebrand domain of ANTXR2 identified from cases of infantile systemic hyalinosis resulted in partial or complete retention of the protein in the endoplasmic reticulum (ER) of transfected HeLa cells and anthrax toxin receptor–deficient Chinese hamster ovary cells, as did a mutation in the transmembrane domain. They speculate that, for certain mutations, assisting the proper folding and surface expression of ANTXR2 by chemical chaperones may allow for rescue of phenotype, as these proteins appeared to be relatively stable in the ER without rapid degradation by endoplasmic-reticulum-associated protein degradation.

Excerpted from Wikipedia’s “ANTXR2” article, available under the CC BY-SA 4.0 licence.

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