Detailed description page of humcfs

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TTN details
Primary information
gene_nameTTN
Humcfs IdHumcfs_830
chromosome_numberchromosome2
nameFRA2G
chrlocation169700001-183000000
cytoband2p31
typeAphidicolin
frequencyCommon
gene_ensembl_idENST00000446966
havana_transcript_idOTTHUMT00000328410
gene_location178640077-178651516
gene_orientation-
exon_idENSE00001724319, ENSE00003807205, ENSE00003809179, ENSE00003806702, ENSE00001666171, ENSE00001648884, ENSE00001734166, ENSE00001608285, ENSE00001690572, ENSE00003804845, ENSE00003809515, ENSE000038078
exon_number14
gene_descriptiontitin
disease_descriptionFamilial dilated cardiomyopathy,TIBIAL MUSCULAR DYSTROPHY, TARDIVE,early pregnancy,Dermatomyositis,Myofibrillar Myopathy,Heart failure,Congenital myopathy (disorder),Prostate carcinoma,Tibial Muscular Dystrophy,Thymoma,Spinal Muscular Atrophy,Adult type dermatomyositis,Myopathy,Epithelioma,HIV Infections,Ischemia,Muscular Dystrophy,Pain,Malignant neoplasm of prostate,Muscular Dystrophy, Duchenne,Coronary Arteriosclerosis,Inflammatory disorder,Atrial Septal Defects,Distal Muscular Dystrophies,Experimental Autoimmune Encephalomyelitis,Myasthenia Gravis,Facial Pain,Down Syndrome,Cardiomyopathy, Dilated,Myopathy, Centronuclear, Autosomal Recessive,Diabetes,Hypertrophic Cardiomyopathy,Limb-girdle muscular dystrophy type 2A,Toxic multinodular goiter,Rheumatoid Arthritis,Myopathy, Early-Onset, with Fatal Cardiomyopathy,Restrictive cardiomyopathy,Eichsfeld type congenital muscular dystrophy,Respiratory Failure,Nemaline Myopathy, Autosomal Recessive,Centronuclear myopathy,Myocardial Ischemia,Mu
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID12620385
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