Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
CASP12 caspase 12 (gene/pseudogene) CASP-12 , CASP12P1 Homo sapiens 9 protein-coding CASP6 , CASP7 , CASP10 , CFLAR , CASP8 , CASP3 , CASP2 , CASP5 , CASP4 , CASP14 , CASP9 608633

Summary

Caspases are cysteine proteases that cleave C-terminal aspartic acid residues on their substrate molecules. This gene is most highly related to members of the ICE subfamily of caspases that process inflammatory cytokines. In rodents, the homolog of this gene mediates apoptosis in response to endoplasmic reticulum stress. However, in humans this gene contains a polymorphism for the presence or absence of a premature stop codon. The majority of human individuals have the premature stop codon and produce a truncated non-functional protein. The read-through codon occurs primarily in individuals of African descent and carriers have endotoxin hypo-responsiveness and an increased susceptibility to severe sepsis. Several alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Feb 2011]

GeneOntology

Gene Loss events - CASP12 (2 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_BNJWYA Physeter catodon Artiodactyla Other Full No 10.1093/gbe/evx187
GL_VNHMXM Balaena mysticetus Artiodactyla LOF (frameshift, premature stop, ss) Full No 10.1016/j.celrep.2014.12.008