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TNXB

Gene

tenascin XB

HGNCHGNC:11976EnsemblENSG00000168477NCBI Gene7148
Locus: gene with protein productLocation: 6p21.33-p21.32

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asTNXB1 · TNXB2 · TNXBS · XBS · XB · HXBL · TN-X · TNX
View full nomenclature history (10)
Previous symbolsTNXB1, TNXB2
Alias symbolsTNXBS, XBS, XB, HXBL, TN-X, TNX
Alias namesHexabrachion-like protein, tenascin-X

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Ehlers-Danlos Syndrome
Genetic Diseases, Inborn

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Tenascins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.