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FAAH2

Chr Xp11.21

fatty acid amide hydrolase 2

Aliases:
RP11-479E16.1, FLJ31204, FAAH-2
MANE:
ENST00000374900.5

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Moderate Evidence (Amber)

  • Intellectual disability

    X-LINKED: hemizygous mutation in males, biallelic mutations in females

Disease associations (Open Targets)

  • hypogonadism

    0.30
  • hypertensive disorder

    0.24
  • type 2 diabetes mellitus

    0.22
  • systemic lupus erythematosus

    0.06
  • Atrophy/Degeneration affecting the central nervous system

    0.04
  • depressive disorder

    0.03
  • heart disorder

    0.02
  • neoplasm

    0.02
  • nonpapillary renal cell carcinoma

    0.01
  • psychiatric disorder

    0.01

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

Fatty-acid amide hydrolase 2

Catalyzes the hydrolysis of endogenous amidated lipids like the sleep-inducing lipid oleamide ((9Z)-octadecenamide), the endocannabinoid anandamide (N-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-ethanolamine), as well as other fatty amides, to their corresponding fatty acids, thereby regulating the signaling functions of these molecules (PubMed:17015445, PubMed:19926788). Hydrolyzes monounsaturated substrate anandamide preferentially as compared to polyunsaturated substrates

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.