Detailed description page of humcfs

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Humcfs_1648 details
Primary information
Humcfs IdHumcfs_1648
chromosome_numberchromosome6
nameFRA6B
chrlocation4200001-7100000
cytoband6p25.1
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000145982
gene_nameFARS2
havana_transcript_idOTTHUMT00000039747
gene_location5404542-5431810
gene_orientation+
exon_idENSE00000973358, ENSE00000973359, ENSE00001743145
exon_number3
gene_descriptionphenylalanyl-tRNA synthetase 2, mitochondrial
disease_descriptionAlpers Syndrome (disorder),Mitochondrial Encephalomyopathies,Epilepsy,Tobacco Use Disorder,Mitochondrial Diseases,Mitochondrial encephalopathy,Encephalopathies,Tremor,Obesity,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14,Diffuse Cerebral Sclerosis of Schilder
miRNA_location5148286-5148308
miRNA_strand.
miRNA_idMIMAT0018120
miRNA_namehsa-miR-3691-5p
miRNA_derived MI0016092
TechniqueYAC cloned
PMID8750194
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank