Gene entry
TNXB
tenascin XB
- Chromosome
- 6
- Cytoband
- 6p21.33-p21.32
- Variants (rsID)
- 54
TNXB is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p21.33-p21.32). Its official name is “tenascin XB”. The reference table lists 54 variants (rsID) for this gene.
Clinically classified variants
16 reference-table entries with clinical significance.
- rs10947230Benignsingle nucleotide variant
- rs12211410Benignsingle nucleotide variant
- rs149995364Benignsingle nucleotide variantEhlers-Danlos syndrome
- rs17201602Benignsingle nucleotide variant
- rs17207895Benignsingle nucleotide variantEhlers-Danlos syndrome
- rs17207923Benignsingle nucleotide variantEhlers-Danlos syndrome
- rs185819Benignsingle nucleotide variantVesicoureteral reflux 8|Ehlers-Danlos syndrome due to tenascin-X deficiency|Ehlers-Danlos syndrome
- rs204885Benignsingle nucleotide variantEhlers-Danlos syndrome
- rs2239689Benignsingle nucleotide variantVesicoureteral reflux 8|Ehlers-Danlos syndrome due to tenascin-X deficiency
- rs41270450Benignsingle nucleotide variantEhlers-Danlos syndrome
- rs41270458Benignsingle nucleotide variantEhlers-Danlos syndrome
- rs61746206Benignsingle nucleotide variantEhlers-Danlos syndrome
- rs61995676Benignsingle nucleotide variantEhlers-Danlos syndrome
- rs121912575Conflicting interpretationssingle nucleotide variantEhlers-Danlos syndrome due to tenascin-X deficiency|See cases|Ehlers-Danlos syndrome
- rs141190850Conflicting interpretationssingle nucleotide variantVesicoureteral reflux 8|Ehlers-Danlos syndrome due to tenascin-X deficiency|Ehlers-Danlos syndrome due to tenascin-X deficiency|Ehlers-Danlos syndrome
- rs184813324Uncertain significancesingle nucleotide variantEhlers-Danlos syndrome due to tenascin-X deficiency|Vesicoureteral reflux 8
Other listed variants
- rs204879
- rs204895
- rs204899
- rs411337
- rs1150755
- rs1269854
- rs2071293
- rs2071295
- rs2269426
- rs2856448
- rs2857009
- rs3096695
- rs3130286
- rs3130287
- rs3134954
- rs3807039
- rs6902493
- rs7766862
- rs7774197
- rs9267796
- rs12153855
- rs12198173
- rs12524441
- rs13199524
- rs17421624
- rs34878747
- rs41268896
- rs57740770
- rs61735731
- rs61737606
- rs61978561
- rs77913858
- rs114188606
- rs115521560
- rs138850364
- rs184878358
- rs185207099
- rs189944258
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.