protein-coding gene of Homo sapiens FA2H 16 16q23 20140408 79152 9606 Bin Zhao, Yue Liu, Oliver He Ensembl:ENSG00000103089 FA2H FAAH FAH1 FAXDC1 GO_0001949 (EC: IEA); GO_0005506 (EC: IEA); GO_0005789 (EC: IEA); GO_0006633 (EC: IEA); GO_0006665 (EC: IEA); GO_0008219 (EC: IEA); GO_0016021 (EC: IEA); GO_0020037 (EC: IEA); GO_0030258 (EC: IEA); GO_0032286 (EC: IEA); GO_0032287 (EC: IEA); GO_0042127 (EC: IEA); GO_0042634 (EC: IEA); GO_0080132 (EC: IEA) HGNC:21197 HPRD:16873 MIM:611026 Official from a nomenclature committee Other designations: fatty acid alpha-hydroxylase|fatty acid hydroxylase domain containing 1|spastic paraplegia 35 (autosomal recessive) PMID: 12477932; 15337768; 16344560; 16713569; 17355976; 18463364; 19068277; 19834535; 19844255; 20104589; 20379614; 21592092; 21599921; 21735565; 22704260; 22925154; 23535410; 23566484; 24299421 SCS7 SPG35 Vega:OTTHUMG00000137603 WEB: http://www.ncbi.nlm.nih.gov/gene fatty acid 2-hydroxylase fatty acid 2-hydroxylase protein-coding