Tenascin X: Difference between revisions
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'''Tenascin X''' is a [[ | |||
{{Infobox protein | |||
| name = Tenascin-X | |||
| image = <!-- Image removed --> | |||
| caption = <!-- Caption removed --> | |||
| symbol = TNXB | |||
| gene = TNXB | |||
| chromosome = 6 | |||
| arm = p | |||
| band = 21.3 | |||
}} | |||
'''Tenascin-X''' is a large [[extracellular matrix]] [[glycoprotein]] that plays a crucial role in the [[structural integrity]] of [[connective tissues]]. It is encoded by the [[TNXB gene]] located on [[chromosome 6]] in humans. | |||
== Function == | == Function == | ||
Tenascin X is | Tenascin-X is involved in the organization and maintenance of the [[extracellular matrix]], which provides structural support to [[tissues]] and influences [[cell behavior]]. It is particularly important in the [[skin]], [[muscles]], and [[blood vessels]]. | ||
== Clinical significance == | == Clinical significance == | ||
Mutations in the TNXB gene can lead to a condition known as [[Ehlers-Danlos syndrome]] type tenascin-X deficient, which is characterized by [[hyperelastic skin]], [[joint hypermobility]], and [[tissue fragility]]. This condition highlights the importance of tenascin-X in maintaining [[tissue integrity]]. | |||
[[ | |||
== | == Interactions == | ||
Tenascin-X interacts with other [[extracellular matrix proteins]] and [[cell surface receptors]], influencing [[cell adhesion]], [[migration]], and [[proliferation]]. These interactions are critical for [[tissue repair]] and [[development]]. | |||
== See also == | == See also == | ||
* [[ | * [[Extracellular matrix]] | ||
* [[Connective tissue]] | |||
* [[Ehlers-Danlos syndrome]] | * [[Ehlers-Danlos syndrome]] | ||
== References == | == References == | ||
<references /> | <references /> | ||
[[ | == External links == | ||
[[Category: | * [https://www.ncbi.nlm.nih.gov/gene/7148 TNXB gene - NCBI] | ||
[[Category: | * [https://ghr.nlm.nih.gov/gene/TNXB TNXB - Genetics Home Reference] | ||
[[Category: | |||
{{Protein-stub}} | |||
{{Ehlers-Danlos syndrome}} | |||
[[Category:Extracellular matrix proteins]] | |||
[[Category:Genes on human chromosome 6]] | |||
[[Category:Glycoproteins]] | |||
Latest revision as of 21:47, 29 December 2024
Tenascin-X is a large extracellular matrix glycoprotein that plays a crucial role in the structural integrity of connective tissues. It is encoded by the TNXB gene located on chromosome 6 in humans.
Function[edit]
Tenascin-X is involved in the organization and maintenance of the extracellular matrix, which provides structural support to tissues and influences cell behavior. It is particularly important in the skin, muscles, and blood vessels.
Clinical significance[edit]
Mutations in the TNXB gene can lead to a condition known as Ehlers-Danlos syndrome type tenascin-X deficient, which is characterized by hyperelastic skin, joint hypermobility, and tissue fragility. This condition highlights the importance of tenascin-X in maintaining tissue integrity.
Interactions[edit]
Tenascin-X interacts with other extracellular matrix proteins and cell surface receptors, influencing cell adhesion, migration, and proliferation. These interactions are critical for tissue repair and development.
See also[edit]
References[edit]
<references />
External links[edit]
