Primary information |
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Humcfs Id | Humcfs_2741 |
chromosome_number | chromosome10 |
name | FRA10C |
chrlocation | 52900001-70600000 |
cytoband | 10q21 |
type | BrdU |
frequency | Common |
gene_ensembl_id | ENSG00000138346 |
gene_name | DNA2 |
havana_transcript_id | OTTHUMT00000407299 |
gene_location | 68414064-68471886 |
gene_orientation | - |
exon_id | ENSE00003462695, ENSE00003303530, ENSE00003734572, ENSE00003714122, ENSE00001772574, ENSE00001712965, ENSE00001729977, ENSE00001641645, ENSE00001647298, ENSE00001596452, ENSE00001794102, ENSE000016272 |
exon_number | 17 |
gene_description | DNA replication helicase/nuclease 2 |
disease_description | PITUITARY DWARFISM I,Fanconi Anemia,PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 6,Malignant neoplasm of urinary bladder,leukemia,Mitochondrial Myopathies,Malignant neoplasm of ovary,Tobacco Use Disorder,FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder),Breast Carcinoma,Myopathy,Ovarian Carcinoma,HIV Infections,Malignant neoplasm of breast,Intrahepatic Cholangiocarcinoma,Seckel syndrome |
miRNA_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | Karyotyping |
PMID | 2579891 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |