Detailed description page of humcfs

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Humcfs_4212 details
Primary information
Humcfs IdHumcfs_4212
chromosome_numberchromosome19
nameFRA19A
chrlocation32400001-59128983
cytoband19q13
type5-azacytidine
frequencyCommon
gene_ensembl_idENSG00000105357
gene_nameMYH14
havana_transcript_idOTTHUMT00000464708
gene_location50203637-50271482
gene_orientation+
exon_idENSE00002991983, ENSE00001125634, ENSE00003730737, ENSE00003733339, ENSE00000899930, ENSE00001616058, ENSE00003745853, ENSE00003717649, ENSE00003722218, ENSE00003748715, ENSE00003743055, ENSE000037542
exon_number24
gene_descriptionmyosin, heavy chain 14, non-muscle
disease_descriptionNonsyndromic Deafness,Tumor Progression,Bardet-Biedl Syndrome,Vascular Diseases,Cardiomyopathies,Neoplasm Metastasis,MYOPATHY, MYOSIN STORAGE (disorder),Chronic kidney disease stage 5,Deafness, Autosomal Dominant 4,Cleft Palate,Cleft Lip,Lymphoma,Cardiomyopathy, Dilated,Hypertrophic Cardiomyopathy,Prostatic Neoplasms,Peripheral Neuropathy,Hearing Loss, Mixed Conductive-Sensorineural,Chronic Kidney Diseases,Kidney Failure, Chronic,Hoarseness,Keloid,PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS,Hearing disability
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID2579891
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