Detailed description page of humcfs

This page displays user query in tabular form.

TNXB details
Primary information
gene_nameTNXB
Humcfs IdHumcfs_1835
chromosome_numberchromosome6
nameFRA6H
chrlocation30400001-46200000
cytoband6p21
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000168477
havana_transcript_idOTTHUMT00000268929
gene_location32098176-32115334
gene_orientation-
exon_idENSE00003664027, ENSE00001705435
exon_number2
gene_descriptiontenascin XB
disease_descriptionDermatitis, Atopic,Ehlers-Danlos syndrome, type 3 (disorder),Lupus Erythematosus, Systemic,Metastatic Carcinoma,Myopathy,VESICOURETERAL REFLUX 8,HIV Infections,Vesico-Ureteral Reflux,Psoriasis,Nasal Polyps,Connective Tissue Diseases,Mesothelioma,Plexiform Neurofibroma,Diabetes Mellitus, Insulin-Dependent,Breast Carcinoma,Joint laxity,Hypermobility syndrome,Spontaneous abortion,Ovarian Carcinoma,Alzheimer's Disease,Chronic active hepatitis,Tumor Progression,Rheumatoid Arthritis,Arthralgia,Neurofibromatosis 1,Ehlers-Danlos Syndrome,Mixed Salivary Gland Tumor,21-hydroxylase deficiency,Congenital adrenal hyperplasia,Hypertensive disease,Cystadenocarcinoma, Serous,Congenital adrenal hyperplasia due to 21 hydroxylase deficiency,Carcinogenesis,Immunologic Deficiency Syndromes,Schizophrenia,Age related macular degeneration,Malignant mesothelioma,Ehlers-Danlos syndrome caused by tenascin-X deficiency,Recurrent joint dislocation
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueBAC cloned
PMID17290399
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank