Detailed description page of humcfs

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SLC33A1 details
Primary information
gene_nameSLC33A1
Humcfs IdHumcfs_1282
chromosome_numberchromosome3
nameFRA3D
chrlocation148900001-160700000
cytoband3p25
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000169359
havana_transcript_idOTTHUMT00000351131
gene_location155827958-155853491
gene_orientation-
exon_idENSE00001513335, ENSE00003581899, ENSE00003611434, ENSE00003627699, ENSE00001813286
exon_number5
gene_descriptionsolute carrier family 33 (acetyl-CoA transporter), member 1
disease_descriptionSpastic Paraplegia 42, Autosomal Dominant,Arteriosclerosis,Heart failure,Prostate carcinoma,Cerebral Ischemia,Peritoneal Fibrosis,Kidney Failure, Acute,Fibrosis, Liver,Hypertension, Renovascular,Hypertensive heart disease,Congenital posterior urethral valves,Coronary Artery Disease,Malignant neoplasm of breast,Malignant neoplasm of pancreas,Vesico-Ureteral Reflux,Coronary heart disease,Fluid overload,Developmental Disabilities,Ischemic Cerebrovascular Accident,Spastic Paraplegia,melanoma,Malignant neoplasm of prostate,Focal glomerulosclerosis,Coronary Arteriosclerosis,Mental Depression,Amyotrophic Lateral Sclerosis,Atherosclerosis,Cardiovascular Diseases,Paraplegia,Myocardial Ischemia,Adenoma,Sensory neuropathy,Conn Syndrome,Myocardial Infarction,Hepatitis C, Chronic,Ischemic stroke,Diabetes Mellitus, Non-Insulin-Dependent,Brain Ischemia,Hypertrophic Cardiomyopathy,Liver carcinoma,Left Ventricular Hypertrophy,Mesial temporal sclerosis,Kidney Diseases,Restenosis,hearing impairment,Essen
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID17567780
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