Target intelligence / Profile preview

Eukaryotic translation elongation factor 1 alpha 1 pseudogene 14 (EEF1A1P14)

Target
EEF1A1P14
Molecular classification
Other (Processed pseudogene)
01

Overview

EEF1A1P14 is a processed pseudogene derived from the EEF1A1 gene family, located at 1q31.3 in the human genome and spanning 1666 nucleotides[2]. It does not encode a functional protein but is one of more than 40 EEF1A1-related pseudogenes dispersed throughout the human genome[2]. While the parent gene EEF1A1 encodes a major translation elongation factor critical for protein biosynthesis, EEF1A1P14 itself has no established protein-coding function. Some EEF1A1 pseudogenes have been weakly associated with various cancers, usually by correlative genomic analyses, but there are no well-characterized functional or pathological roles for EEF1A1P14 specifically[2][3][4][5]. EEF1A1P14 and related pseudogenes are sometimes transcribed and may act as regulatory non-coding RNAs affecting the expression of the parental EEF1A1 gene or other genes; however, functional details for EEF1A1P14 are not available[2]. In summary, EEF1A1P14 is a non-coding processed pseudogene, generally not considered a therapeutic target, with no direct biological, mechanistic, or clinical roles described to date[2][4][5].

Other names
EEF1AL12Eukaryotic translation elongation factor 1 alpha-like 12 pseudogeneEukaryotic translation elongation factor 1 alpha 1 (EEF1A1) pseudogene
02

Mechanism of action

No established mechanism since there are no drugs targeting this pseudogene.

03

Biological functions

Other (as a pseudogene, EEF1A1P14 itself does not encode a functional protein; however, pseudogenes can impact gene regulation, for example by acting as competing endogenous RNAs or affecting parental gene expression in a regulatory manner, although this is generally speculative for EEF1A1P14)
04

Disease associations

Cancer (listed in association with cancer types including liver, rectal, ovarian, oral squamous cell carcinoma, and breast cancer, but these associations are weak or speculative and based primarily on gene location/correlative studies—not well established mechanistic roles)

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