Detailed description page of humcfs

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Humcfs_4921 details
Primary information
Humcfs IdHumcfs_4921
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000105143
gene_nameSLC1A6
havana_transcript_idOTTHUMT00000466290
gene_location14971750-15022990
gene_orientation-
exon_idENSE00003074195, ENSE00003493206, ENSE00003171765
exon_number3
gene_descriptionsolute carrier family 1 (high affinity aspartate/glutamate transporter), member 6
disease_descriptionHyperparathyroidism, Secondary,Leukemia, T-Cell,Major Depressive Disorder,Bipolar Disorder,Unipolar Depression,Schizophrenia,Spinocerebellar Ataxia Type 5,Weight Gain,Weight Gain Adverse Event
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank