Target intelligence / Profile preview

Major facilitator superfamily domain-containing 14A (MFSD14A)

Target
MFSD14A
Molecular classification
Transporter, Solute carrier (atypical SLC), Major facilitator superfamily (MFS)
01

Overview

Major facilitator superfamily domain-containing 14A (MFSD14A, also known as HIAT1 or SLC71A1) is a transmembrane protein classified as an atypical solute carrier belonging to the MFS superfamily[1][4]. MFSD14A is highly conserved across species and is widely expressed in the brain and peripheral tissues, with notable abundance in the hippocampus and Sertoli cells of the testes[4][7]. Functional studies in both vertebrates and invertebrates (e.g., crab and mouse) indicate MFSD14A is a sodium-dependent ammonia transporter involved in cellular ammonia detoxification and homeostasis[2][3]. Disruption of the MFSD14A gene in mice causes male infertility with globozoospermia due to failed spermiogenesis, indicating a critical role in acrosome formation, sperm head condensation, and mitochondrial positioning[7]. MFSD14A expression is regulated by nutritional status and may be involved in energy metabolism, though its exact substrate specificity in humans is not yet well-defined[4]. No drugs currently target MFSD14A, and its function as a transporter with physiological relevance positions it as a potential but yet unexploited therapeutic target, especially in reproductive and metabolic biology.

Other names
Hippocampus abundant transcript 1 proteinHIAT1DKFZP564L0864Putative tetracycline transporter-like proteinHAIT1MFSD14Ahippocampus abundant gene transcript 1major facilitator superfamily domain containing 14Atetracycline transporter-like proteinSLC71A1
02

Mechanism of action

No characterized mechanism of drug action targeting MFSD14A; protein likely mediates solute/ammonia transport based on homology and recent functional data

03

Biological functions

Transporter activity (likely organic solutes, ammonia transport)Cellular homeostasis (ammonia regulation)Spermatogenesis (acrosome formation, sperm head condensation, mitochondrial localization)
04

Disease associations

Infertility (male mice with gene disruption are sterile due to globozoospermia)Reproductive disorders (globozoospermia and failed spermiogenesis)
05

Safety considerations

Disruption leads to male infertility in mice (globozoospermia) but no other major safety concerns reported; biological role suggests risk if targeted in reproductive biology[7].

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