PAFAH1B2

Last updated

PAFAH1B2
Protein PAFAH1B2 PDB 1fxw.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases PAFAH1B2 , HEL-S-303, platelet activating factor acetylhydrolase 1b catalytic subunit 2
External IDs OMIM: 602508; MGI: 108415; HomoloGene: 1932; GeneCards: PAFAH1B2; OMA:PAFAH1B2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001184746
NM_001184747
NM_001184748
NM_001309431
NM_002572

Contents

NM_008775

RefSeq (protein)

NP_001171675
NP_001171676
NP_001171677
NP_001296360
NP_002563

Location (UCSC) Chr 11: 117.14 – 117.18 Mb Chr 9: 45.96 – 46.01 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Platelet-activating factor acetylhydrolase IB subunit beta is an enzyme that in humans is encoded by the PAFAH1B2 gene. [5] [6] [7]

Interactions

PAFAH1B2 has been shown to interact with PAFAH1B1. [8]

See also

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000168092 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000003131 Ensembl, 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. Adachi H, Tsujimoto M, Hattori M, Arai H, Inoue K (Apr 1997). "Differential tissue distribution of the beta- and gamma-subunits of human cytosolic platelet-activating factor acetylhydrolase (isoform I)". Biochemical and Biophysical Research Communications. 233 (1): 10–3. doi:10.1006/bbrc.1997.6383. PMID   9144386.
  6. Moro F, Arrigo G, Fogli A, Bernard L, Carrozzo R (Jul 1998). "The beta and gamma subunits of the human platelet-activating factor acetyl hydrolase isoform Ib (PAFAH1B2 and PAFAH1B3) map to chromosome 11q23 and 19q13.1, respectively". Genomics. 51 (1): 157–9. doi:10.1006/geno.1998.5322. PMID   9693049.
  7. "Entrez Gene: PAFAH1B2 platelet-activating factor acetylhydrolase, isoform Ib, beta subunit 30kDa".
  8. Sweeney KJ, Clark GD, Prokscha A, Dobyns WB, Eichele G (Apr 2000). "Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain development". Mechanisms of Development. 92 (2): 263–71. doi: 10.1016/S0925-4773(00)00242-2 . PMID   10727864.

Further reading