Detailed description page of humcfs

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SLC1A3 details
Primary information
gene_nameSLC1A3
Humcfs IdHumcfs_1424
chromosome_numberchromosome5
nameFRA5A
chrlocation28900001-42500000
cytoband5p13
typeBrdU
frequencyCommon
gene_ensembl_idENSG00000079215
havana_transcript_idOTTHUMT00000366898
gene_location36608178-36629588
gene_orientation+
exon_idENSE00002041086, ENSE00002041668
exon_number2
gene_descriptionsolute carrier family 1 (glial high affinity glutamate transporter), member 3
disease_descriptionSeizures,Spinocerebellar Ataxia Type 1,Anxiety Disorders,IGA Glomerulonephritis,Colorectal Cancer,Spinocerebellar Ataxia Type 7,Unipolar Depression,Autistic Disorder,HIV Infections,Attention deficit hyperactivity disorder,Synovial Cyst,Weight Gain,Multiple Sclerosis,Alternating hemiplegia of childhood,Glaucoma,Impaired cognition,EPISODIC ATAXIA, TYPE 6 (disorder),Major Depressive Disorder,Hemiplegia,Episodic Ataxia,Colorectal Carcinoma,Hemiplegia, Crossed,Fatal Familial Insomnia,Prion Diseases,Frontotemporal Lobar Degeneration,Myxoid cyst,Epilepsy,Schizophrenia,Weight Gain Adverse Event,Gilles de la Tourette syndrome,Childhood Osteosarcoma,GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO (finding),Ataxia,Leukemia, Lymphocytic, Acute, L1,Hyperglycemia,Dementia,Migraine Disorders
miRNA_location36147946-36147967
miRNA_strand-
miRNA_idMIMAT0026617
miRNA_namehsa-miR-580-5p
miRNA_derived MI0003587
TechniqueKaryotyping
PMID16981993
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank