Detailed description page of humcfs

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COMP details
Primary information
gene_nameCOMP
Humcfs IdHumcfs_4793
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000105664
havana_transcript_idOTTHUMT00000403456
gene_location18782773-18791305
gene_orientation-
exon_idENSE00003143164, ENSE00003190692, ENSE00003159325, ENSE00003218232, ENSE00003143260, ENSE00003146191, ENSE00003192317, ENSE00003631787, ENSE00002994550, ENSE00003111278, ENSE00003116721, ENSE000031286
exon_number18
gene_descriptioncartilage oligomeric matrix protein
disease_descriptionArteriosclerosis,Hypercholesterolemia, Familial,Pseudoachondroplasia,Superficial ulcer,Disorder of skeletal system,Localized scleroderma,Hydrops Fetalis,Arthritis, Collagen-Induced,Experimental Organism Basal Cell Carcinoma,Joint Instability,Oral Submucous Fibrosis,Cartilage Diseases,HIV Infections,Dwarfism,Coronary Artery Disease,Familial Mediterranean Fever,Arthropathy,Hyperuricemia,Osteoarthritis, Knee,Atherosclerosis,nervous system disorder,Degenerative polyarthritis,Nodule,Mucopolysaccharidosis IV,Carcinogenesis,alpha-Thalassemia,Hyperalgesia, Thermal,Alzheimer's Disease,Erythema,Epiphyseal dysplasia, multiple, 1,Malignant tumor of colon,Chondrodysplasia,Rheumatoid Arthritis,Metabolic Diseases,Scleroderma,alpha^+^ Thalassemia,Arthritis,Medulloblastoma,Thalassemia,Systemic Scleroderma,Sarcoma,Amyloidosis,Multiple Epiphyseal Dysplasia,Osteochondrodysplasias,Chronic arthritis,Glioma,alpha^0^ Thalassemia,Dysplastic Nevus,Keloid,Pseudochondroplasia,Arthritis, Adjuvant-Induced,Homozygou
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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