1. Gene
  2. CASP12 - caspase 12 (gene/pseudogene) Gene

CASP12 - caspase 12 (gene/pseudogene) Gene

Homo sapiens

Also known as CASP-12; CASP12P1

Gene ID: 100506742 | Gene type: protein coding

About CASP12

Cytogenetic location: 11q22.3 Genomic coordinates (GRCh38): 11:104,885,718-104,898,460 (from NCBI)

This gene has 12 transcripts (splice variants), 273 orthologues and 16 paralogues. Broad expression in ovary (RPKM 2.1), endometrium (RPKM 1.1) and 14 other tissues.

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]

CASP12 Products(11)

mRNA Protein Name
NR_000035.2
NR_034063.4
NR_034064.4
NM_001191016.3 NP_001177945.2 inactive caspase-12
NR_034071.4
NR_034066.4
NR_034061.4
NR_034068.4
NR_034067.4
NR_034065.4
NR_034070.4

CASP12 Protein Structure

CARD

CARD: Caspase recruitment domain (13 - 89)

Peptidase_C14

Peptidase_C14: Caspase domain (103 - 336)

  • 0
  • 100
  • 200
  • 300
  • 341 a.a.
Protein Preferred Names Protein Names

inactive caspase-12

caspase 12 pseudogene 1

Related Diseases

Diseases Alias
Prion Disease

Spongiform Encephalopathy

Transmissible Spongiform Encephalopathies

Prion Diseases

Prion Disease Pathway

Transmissible Spongiform Encephalopathy

Prion Induced Disorder

Prion Protein Disease

Inherited Human Transmissible Spongiform Encephalopathies

Prion Protein Diseases

Prion-Associated Disorders

Prion-Induced Disorders

Transmissible Dementias

Tses

Human Prion Disease

Tse

Encephalopathy, Transmissible Spongiform

Prion Disease, Susceptibility To

Spongiform Encephalopathies

Human Transmissible Spongiform Encephalopathies, Inherited

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus CASP12 MGD MGI:1312922
Rattus norvegicus CASP12 RGD RGD:621758