Primary information |
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Humcfs Id | Humcfs_4921 |
chromosome_number | chromosome19 |
name | FRA19B |
chrlocation | 1-20000000 |
cytoband | 19p13 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000105143 |
gene_name | SLC1A6 |
havana_transcript_id | OTTHUMT00000466290 |
gene_location | 14971750-15022990 |
gene_orientation | - |
exon_id | ENSE00003074195, ENSE00003493206, ENSE00003171765 |
exon_number | 3 |
gene_description | solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6 |
disease_description | Hyperparathyroidism, Secondary,Leukemia, T-Cell,Major Depressive Disorder,Bipolar Disorder,Unipolar Depression,Schizophrenia,Spinocerebellar Ataxia Type 5,Weight Gain,Weight Gain Adverse Event |
miRNA_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | FISH |
PMID | 3568428 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |