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TNXB - tenascin XB

Synonym(s) : TNXBS, XB, XBS
Previous symbols and names : TNXB1, TNXB2
Type : gene with protein product
Chromosomal location : 6p21.33-p21.32
OMIM: 600985
HGNC: 11976
UniProtKB: P22105
Genatlas: TNXB
GenCC: TNXB
Ensembl: ENSG00000168477
IUPHAR-DB: -
Reactome: P22105
LOVD: TNXB

Diseases list

Disease-causing germline mutation(s) in Classical-like Ehlers-Danlos syndrome type 1 ORPHA:230839
Disease-causing germline mutation(s) in Familial vesicoureteral reflux ORPHA:289365

: Assessed

Additional information

Patient-centred resources for this gene

Diagnostic tests (75)

Research activities on this gene

Specialised Social Services

Eurordis directory

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