FABP2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

FABP2

Fatty acid-binding protein 2 (FABP2), also known as Intestinal-type fatty acid-binding protein (I-FABP), is a protein that in humans is encoded by the FABP2 gene.[5]

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FABP2
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Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesFABP2, FABPI, I-FABP, fatty acid binding protein 2
External IDsOMIM: 134640; MGI: 95478; HomoloGene: 107; GeneCards: FABP2; OMA:FABP2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000134

NM_007980

RefSeq (protein)

NP_000125

NP_032006

Location (UCSC)Chr 4: 119.32 – 119.32 MbChr 3: 122.69 – 122.69 Mb
PubMed search[3][4]
Wikidata
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Function

The intracellular fatty acid-binding proteins (FABPs) belong to a multigene family with nearly twenty identified members. FABPs are divided into at least three distinct types, namely the hepatic-, intestinal- and cardiac-type. They form 14-15 kDa proteins and are thought to participate in the uptake, intracellular metabolism and/or transport of long-chain fatty acids. They may also be responsible in the modulation of cell growth and proliferation. Intestinal fatty acid-binding protein 2 gene contains four exons and is an abundant cytosolic protein in small intestine epithelial cells.[5]

Clinical significance

This gene has a polymorphism at codon 54 that identified an alanine-encoding allele and a threonine-encoding allele. Thr-54 protein is associated with increased fat oxidation and insulin resistance.[5]

References

Further reading

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