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NUT family member 2F (NUTM2F)
- Target
- NUTM2F
- Molecular classification
- Other (protein of unknown functional family/role; not classified as receptor, enzyme, transporter, etc.)
01
Overview
NUT family member 2F is a human protein encoded by the NUTM2F gene. It is a protein of 756 amino acids with a molecular weight of approximately 80.8 kDa[4][5]. The gene is associated with corneal dystrophy, posterior polymorphous types 1 and 3, but its biological function and precise molecular roles are currently not characterized in the scientific literature[3][4][5]. It does not belong to well-known receptor, enzyme, transporter, or transcription factor families based on available data, and there are no direct links to drugs, biomarker utility, or major safety issues. At present, NUTM2F should not be considered a validated therapeutic target due to lack of evidence for such a role.
- Other names
- NUTM2FFAM22FDKFZp434I1117NUTMFFamily with sequence similarity 22, member FProtein FAM22F
02
Biological functions
Unknown (no definitive functional annotation for signaling, cell cycle, apoptosis, etc. publicly available)
03
Disease associations
Other (associated with corneal dystrophy, posterior polymorphous, type 1 and 3; not known for major roles in cancer or key therapeutic areas)
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