Detailed description page of humcfs

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Humcfs_4638 details
Primary information
Humcfs IdHumcfs_4638
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000130304
gene_nameSLC27A1
havana_transcript_idOTTHUMT00000464146
gene_location17470489-17504986
gene_orientation+
exon_idENSE00001431578, ENSE00003195451, ENSE00003678902, ENSE00003200781, ENSE00003546677, ENSE00003481513, ENSE00003619619, ENSE00003641665, ENSE00003682743, ENSE00003575578, ENSE00001703050, ENSE000015055
exon_number13
gene_descriptionsolute carrier family 27 (fatty acid transporter), member 1
disease_descriptionMultiple Endocrine Neoplasia Type 2a,Metabolic Syndrome X,Overweight,Cardiovascular Diseases,Hyperlipidemia,Insulin resistance syndrome,Insulin Resistance,Impaired glucose tolerance,Myocardial Infarction,Hyperinsulinism,Obesity,Diabetes Mellitus, Non-Insulin-Dependent
miRNA_location13874910-13874932
miRNA_strand+
miRNA_idMIMAT0002821
miRNA_namehsa-miR-181d-5p
miRNA_derived MI0003139
TechniqueFISH
PMID3568428
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank