Detailed description page of humcfs

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ATXN2 details
Primary information
gene_nameATXN2
Humcfs IdHumcfs_3523
chromosome_numberchromosome12
nameFRA12E
chrlocation109000001-133851895
cytoband12q24
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000204842
havana_transcript_idOTTHUMT00000257363
gene_location111453320-111456112
gene_orientation-
exon_idENSE00001929663, ENSE00001840067
exon_number2
gene_descriptionataxin 2
disease_descriptionFrontotemporal dementia,Lupus Erythematosus, Systemic,Obesity, Abdominal,Extrapyramidal sign,Motor Neuron Disease,Obesity,Juvenile rheumatoid arthritis,Amyotrophic Lateral Sclerosis,Vitiligo,Genomic Instability,Pick Disease of the Brain,Hyperphagia,Ataxias, Hereditary,Nystagmus, End-Position,Spastic Paraplegia, Hereditary,Neurodegenerative Disorders,Dystonia,Atrophy, Muscular, Spinobulbar,Kidney Failure, Chronic,Blood pressure finding,Dyskinetic syndrome,Ophthalmoparesis,Nervous system--Degeneration,Colonic Neoplasms,Sarcoma,Spinocerebellar Ataxia 10,Seizures,Sleep disturbances,Retinal Degeneration,Neuroblastoma,Diabetes Mellitus, Insulin-Dependent,Cerebellar Diseases,Cerebellar atrophy,Alzheimer's Disease,Central neuroblastoma,Celiac Disease,TDP-43 Proteinopathies,Cerebellar Ataxia,Spinocerebellar Ataxia Type 1,Spinocerebellar Ataxia Type 2,Autosomal Dominant Parkinsonism,Spinocerebellar Ataxia Type 7,Olivopontocerebellar Atrophies,Cardiovascular Diseases,Chronic Kidney Diseases,Chore
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID14526166
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