Detailed description page of humcfs
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PGD details |
| Primary information | |
|---|---|
| gene_name | PGD |
| Humcfs Id | Humcfs_37 |
| chromosome_number | chromosome1 |
| name | FRA1A |
| chrlocation | 1-28000000 |
| cytoband | 1p36 |
| type | Aphidicolin |
| frequency | Common |
| gene_ensembl_id | ENSG00000142657 |
| havana_transcript_id | OTTHUMT00000005404 |
| gene_location | 10399112-10417509 |
| gene_orientation | + |
| exon_id | ENSE00001952258, ENSE00003560207, ENSE00003787396, ENSE00003788764, ENSE00003623710, ENSE00003790627 |
| exon_number | 6 |
| gene_description | phosphogluconate dehydrogenase |
| disease_description | Squamous cell carcinoma,Fragile X Syndrome,Asthma,Streak gonad,Paresis,Adenocarcinoma,Malignant neoplasm of esophagus,Myotonic Dystrophy,Hepatitis B, Chronic,Sickle cell-beta-thalassemia,Malaria,Congenital chromosomal disease,Disorder characterized by eosinophilia,Down Syndrome,Cervix carcinoma,Squamous cell carcinoma of esophagus,Esophageal Neoplasms,Liver carcinoma,Eosinophilic disorder,IMMUNE SUPPRESSION,Disorder of endocrine ovary,Thalassemia,Neurofibromatosis 1,Esophageal carcinoma,Eosinophilia,Cooley's anemia,Congenital Myotonic Dystrophy,Meckel syndrome type 3,Polycystic Kidney, Autosomal Dominant,Leishmaniasis, Cutaneous,Optic Atrophy, Hereditary, Leber,Azoospermia,Cancer Cell Growth,Muscle Weakness,Malignant tumor of cervix,Liver neoplasms |
| miRNA_location | 24919345-24919365 |
| miRNA_strand | - |
| miRNA_id | MIMAT0027364 |
| miRNA_name | hsa-miR-6731-3p |
| miRNA_derived | MI0022576 |
| Technique | Karyotyping |
| PMID | 1322577 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |