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Tigger transposable element-derived protein 6 (TIGD6)

Target
TIGD6
Molecular classification
Other, DNA transposon-derived protein, helix-turn-helix CENPB-type domain containing (pogo superfamily, tigger subfamily)
01

Overview

Tigger transposable element-derived protein 6 (TIGD6) is a human protein encoded by the TIGD6 gene, a member of the tigger subfamily of the pogo superfamily of DNA-mediated transposons[1][3]. These proteins are evolutionarily related to DNA transposases found in lower organisms, such as fungi and nematodes, and are distantly related to the Tc1/mariner family of transposases[1][3]. TIGD6 is structurally similar to mammalian centromere protein B and likely retains nucleic acid binding capacity but is not known to possess transposase enzymatic activity[3]. Its precise biological function in humans is not well defined; the primary annotation is based on sequence homology and structural domains, such as the helix-turn-helix CENPB-type domain[1]. Published associations link TIGD6 with rare neurodevelopmental disorders, but there is no evidence for a direct role in common human diseases or its utility as a therapeutic target[3]. TIGD6 encodes a domesticated transposon-derived protein of unknown physiological function in humans[1][3]. It is not currently recognized as a therapeutic, diagnostic, or pharmacological target. Most information on TIGD6 focuses on its evolutionary origin, molecular structure, and rare disease associations. No drugs or biomarker applications are described.

Other names
TIGD6Tigger transposable element-derived protein 6DKFZp761E2110TIGD6_HUMANPrevious GeneCards identifiers (e.g., GC05M149442)
02

Biological functions

Component of the tigger subfamily of DNA-mediated transposonsParalogous to genes involved in nucleic acid binding, structurally similar to centromere protein BPotential involvement in genome stability and epigenetic regulation (suggested by analogy with related proteins but not experimentally established for TIGD6 itself)
03

Disease associations

Neurodevelopmental disorders (specifically, associations with Intellectual Developmental Disorder, Autosomal Dominant 22)Associations are limited and not well established; no strong evidence connects TIGD6 directly to major human diseases apart from rare Mendelian neurodevelopmental associations

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