Detailed description page of humcfs

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WNT10B details
Primary information
gene_nameWNT10B
Humcfs IdHumcfs_3355
chromosome_numberchromosome12
nameFRA12A
chrlocation46400001-54900000
cytoband12q13.1
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000169884
havana_transcript_idOTTHUMT00000319867
gene_location48970120-48970889
gene_orientation-
exon_idENSE00003501836, ENSE00001319004, ENSE00001757310
exon_number3
gene_descriptionwingless-type MMTV integration site family, member 10B
disease_descriptionMalignant neoplasm of stomach,Cervix carcinoma,Stomach Carcinoma,Osteosarcoma of bone,Osteoporosis, Postmenopausal,Triple Negative Breast Neoplasms,Neoplasm Metastasis,Malignant neoplasm of breast,Breast Carcinoma,Split-Hand/Foot Malformation,Amyotrophic Lateral Sclerosis,Mammary Neoplasms,SPLIT-HAND/FOOT MALFORMATION 6 (disorder),Endometrial Carcinoma,Pathological fracture,Rheumatoid Arthritis,Carcinogenesis,Obesity,Anoxia,Ectrodactyly,Osteosarcoma,Malignant neoplasm of ovary,Malignant tumor of cervix
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID8833161
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