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Mixed lineage kinase domain like pseudokinase

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(Redirected from MLKL) Protein-coding gene in the species Homo sapiens
MLKL
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2MSV, 4M67, 4MWI

Identifiers
AliasesMLKL, hmixed lineage kinase domain-like, mixed lineage kinase domain like pseudokinase
External IDsOMIM: 615153; MGI: 1921818; HomoloGene: 77416; GeneCards: MLKL; OMA:MLKL - orthologs
Gene location (Human)
Chromosome 16 (human)
Chr.Chromosome 16 (human)
Chromosome 16 (human)Genomic location for MLKLGenomic location for MLKL
Band16q23.1Start74,671,855 bp
End74,700,960 bp
Gene location (Mouse)
Chromosome 8 (mouse)
Chr.Chromosome 8 (mouse)
Chromosome 8 (mouse)Genomic location for MLKLGenomic location for MLKL
Band8|8 E1Start112,038,429 bp
End112,064,809 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • granulocyte

  • monocyte

  • blood

  • spleen

  • upper lobe of left lung

  • appendix

  • myocardium of left ventricle

  • right lung

  • pancreatic epithelial cell

  • mucosa of ileum
Top expressed in
  • bone marrow

  • epithelium of stomach

  • stroma of bone marrow

  • endothelial cell of lymphatic vessel

  • duodenum

  • transitional epithelium of urinary bladder

  • Paneth cell

  • subcutaneous adipose tissue

  • colon

  • jejunum
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

197259

74568

Ensembl

ENSG00000168404

ENSMUSG00000012519

UniProt

Q8NB16

Q9D2Y4

RefSeq (mRNA)

NM_001142497
NM_152649

NM_029005
NM_001310613

RefSeq (protein)

NP_001135969
NP_689862

NP_001297542
NP_083281

Location (UCSC)Chr 16: 74.67 – 74.7 MbChr 8: 112.04 – 112.06 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Mixed lineage kinase domain like pseudokinase (MLKL) is a protein that in humans is encoded by the MLKL gene.

Function

This gene belongs to the protein kinase superfamily. The encoded protein contains a protein kinase-like domain; however, is thought to be inactive because it lacks several residues required for activity. This protein plays a critical role in tumor necrosis factor (TNF)-induced necroptosis, a programmed cell death process, via interaction with receptor-interacting protein 3 (RIP3), which is a key signaling molecule in necroptosis pathway. Inhibitor studies and knockdown of this gene inhibited TNF-induced necrosis.

Influence in diseases

High levels of this protein and RIP3 are associated with inflammatory bowel disease in children. Alternatively spliced transcript variants have been described for this gene. . A unique neurodegenerative disease has been reported in association with a homozygous frameshift mutation, rs561839347, in MLKL that causes replacement of part of the C-terminal pseudokinase domain with a 21-residue sequence of random amino acids.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000168404Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000012519Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Mixed lineage kinase domain like pseudokinase". Retrieved 2017-12-31.
  6. Faergeman SL, Evans H, Attfield KE, Desel C, Kuttikkatte SB, Sommerlund M, et al. (2020). "A novel neurodegenerative spectrum disorder in patients with MLKL deficiency". Cell Death & Disease. 11 (5): 303. doi:10.1038/s41419-020-2494-0. PMC 7195448. PMID 32358523. Art. No. 303.

Further reading


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