Detailed description page of humcfs
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ATP1A3 details |
Primary information | |
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gene_name | ATP1A3 |
Humcfs Id | Humcfs_4397 |
chromosome_number | chromosome19 |
name | FRA19A |
chrlocation | 32400001-59128983 |
cytoband | 19q13 |
type | 5-azacytidine |
frequency | Common |
gene_ensembl_id | ENSG00000105409 |
havana_transcript_id | OTTHUMT00000490545 |
gene_location | 41988476-41993864 |
gene_orientation | - |
exon_id | ENSE00003465025, ENSE00003794448 |
exon_number | 2 |
gene_description | ATPase, Na+/K+ transporting, alpha 3 polypeptide |
disease_description | DYSTONIA 12,Epilepsy,Myotonic Dystrophy,Retinoschisis, Juvenile, X-Linked,Heart failure,MIGRAINE, FAMILIAL HEMIPLEGIC, 2,Dystonia, Primary,Movement Disorders,Dystonia 3, Torsion, X-Linked,Parkinsonian Disorders,Motor disturbances,Congenital Myotonic Dystrophy,Motor symptoms,CAPOS syndrome,nervous system disorder,Degenerative polyarthritis,Microcephaly,Tremor,Alternating hemiplegia of childhood,Neonatal infection,ALTERNATING HEMIPLEGIA OF CHILDHOOD 2,Neurologic Symptoms,Ventricular Dysfunction, Left,Dystonia,Septicemia,Bipolar Disorder,Familial Dystonia,Motor Disorders,Ataxia,Dystonia Disorders |
miRNA_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | Karyotyping |
PMID | 2579891 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |