TNXA gene

Known as: TNXA, HXBL, XA 
 
National Institutes of Health

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TNXB gene

Papers overview

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2014
2014
Long noncoding RNA expression signatures of bladder cancer revealed by microarray
Dysregulation of long noncoding RNAs (lncRNAs) has been regarded as a primary feature of several human cancers. However, the… (More)
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2011
2011
Analysis of the CYP21A2 gene with intergenic recombination and multiple gene deletions in the RCCX module.
The most frequent bimodular RCCX module of the RP1-C4A-CYP21A1P-TNXA-RP2-C4B-CYP21A2-TNXB gene sequence is located on chromosome… (More)
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2009
2009
Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: a comparison of Asian-Indian and European American populations.
Inter-individual gene copy-number variations (CNVs) probably afford human populations the flexibility to respond to a variety of… (More)
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Review
2005
Review
2005
Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module.
Two types of chimeric RCCX modules found in chromosome 6p21.3 are the chimeras CYP21P/CYP21 and TNXA/TNXB. The CYP21P-specific… (More)
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2004
2004
PCR-based detection of the CYP21 deletion and TNXA/TNXB hybrid in the RCCX module.
Detection of the CYP21 deletion in congenital adrenal hyperplasia (CAH) in the RCCX module has been previously done by Southern… (More)
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2004
2004
Exclusion of candidate genes in a family with arterial tortuosity syndrome.
Arterial tortuosity syndrome (ATS) is a rare hereditary disorder with variable clinical presentation including tortuosity and… (More)
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2000
2000
Organizations and gene duplications of the human and mouse MHC complement gene clusters.
The MHC complement gene cluster (MCGC) in most people contains thirteen structural genes, pseudogenes and gene segments. Novel… (More)
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Highly Cited
1999
Highly Cited
1999
Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX…
The frequent variations of human complement component C4 gene size and gene numbers, plus the extensive polymorphism of the… (More)
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1999
1999
Homozygous deletion of the CYP21A-TNXA-RP2-C4B gene region conferring C4B deficiency associated with recurrent respiratory infections.
The central class III region of the human major histocompatibility complex contains highly polymorphic genes that are associated… (More)
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1999
1999
An unequal crossover between the RCCX modules of the human MHC leading to the presence of a CYP21B gene and a tenascin TNXB/TNXA-RP2 recombinant between C4A and C4B genes in a patient with juvenile…
The RCCX module of the human MHC class III region is comprised of four genes arranged in tandem: RP, complement C4, steroid 21… (More)
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