Primary information |
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Humcfs Id | Humcfs_1648 |
chromosome_number | chromosome6 |
name | FRA6B |
chrlocation | 4200001-7100000 |
cytoband | 6p25.1 |
type | Aphidicolin |
frequency | Common |
gene_ensembl_id | ENSG00000145982 |
gene_name | FARS2 |
havana_transcript_id | OTTHUMT00000039747 |
gene_location | 5404542-5431810 |
gene_orientation | + |
exon_id | ENSE00000973358, ENSE00000973359, ENSE00001743145 |
exon_number | 3 |
gene_description | phenylalanyl-tRNA synthetase 2, mitochondrial |
disease_description | Alpers Syndrome (disorder),Mitochondrial Encephalomyopathies,Epilepsy,Tobacco Use Disorder,Mitochondrial Diseases,Mitochondrial encephalopathy,Encephalopathies,Tremor,Obesity,COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14,Diffuse Cerebral Sclerosis of Schilder |
miRNA_location | 5148286-5148308 |
miRNA_strand | . |
miRNA_id | MIMAT0018120 |
miRNA_name | hsa-miR-3691-5p |
miRNA_derived | MI0016092 |
Technique | YAC cloned |
PMID | 8750194 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |