FABP2
fatty acid binding protein 2
Summary
The protein encoded by this gene is an intracellular fatty acid-binding protein that participates in the uptake, intracellular metabolism, and transport of long-chain fatty acids. The encoded protein is also involved in the modulation of cell growth and proliferation. This protein binds saturated long-chain fatty acids with high affinity, and may act as a lipid sensor to maintain energy homeostasis. [provided by RefSeq, Aug 2017]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11724758 | 4:120,239,878 | G/A | 3 prime UTR variant | — |
| rs9999724 | 4:120,239,944 | C/T | — | benign |
| rs2964 | 4:120,240,131 | T/C | — | benign |
| rs1511024 | 4:120,240,181 | C/T | — | benign |
| rs1511025 | 4:120,240,238 | T/C | — | benign |
| rs1358257083 | 4:120,240,722 | A/G | — | uncertain significance |
| rs375920710 | 4:120,240,735 | C/T | — | uncertain significance |
| rs753335773 | 4:120,240,753 | G/A | — | uncertain significance |
| rs780387309 | 4:120,240,794 | G/A | — | uncertain significance |
| rs12711071 | 4:120,240,934 | T/C | — | benign |
| rs12510269 | 4:120,241,646 | A/G | — | benign |
| rs12506610 | 4:120,241,659 | T/C | — | benign |
| rs10003567 | 4:120,241,674 | C/T | — | benign |
| rs11935130 | 4:120,241,725 | C/A | — | benign |
| rs4834770 | 4:120,241,849 | A/G | — | benign |
| rs1799883 | 4:120,241,902 | G/A | missense variant | benign |
| rs141065396 | 4:120,241,918 | T/G | — | likely benign |
| rs752892343 | 4:120,241,931 | C/T | — | uncertain significance |
| rs2545699598 | 4:120,241,989 | T/C | — | likely benign |
| rs201640311 | 4:120,241,997 | C/T | — | uncertain significance |
| rs10006259 | 4:120,242,145 | C/T | — | benign |
| rs6823963 | 4:120,242,164 | A/C | — | benign |
| rs28652763 | 4:120,242,312 | C/T | — | benign |
| rs1397613 | 4:120,242,929 | G/T | — | benign |
| rs714899 | 4:120,243,035 | G/A | — | benign |
| rs5861422 | 4:120,243,337 | — | — | benign |
| rs1397614 | 4:120,243,352 | C/T | — | benign |
| rs6857641 | 4:120,243,511 | T/C | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.