Primary information |
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Humcfs Id | Humcfs_2637 |
chromosome_number | chromosome10 |
name | FRA10A |
chrlocation | 97000000-1089500001 |
cytoband | 10q23.3 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000014919 |
gene_name | COX15 |
havana_transcript_id | OTTHUMT00000049819 |
gene_location | 99711844-99732100 |
gene_orientation | - |
exon_id | ENSE00001452834, ENSE00000719584, ENSE00000811283, ENSE00000719603, ENSE00003264063, ENSE00003320905, ENSE00003342377, ENSE00000811288, ENSE00001839320 |
exon_number | 9 |
gene_description | cytochrome c oxidase assembly homolog 15 (yeast) |
disease_description | Leigh Disease,Hypertrophic Cardiomyopathy,Cytochrome-c Oxidase Deficiency,Myasthenic Syndrome due to Mutation in SCN4A,CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2,Cardiomyopathies,Alzheimer's Disease |
miRNA_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | Karyotyping |
PMID | 3879149 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |