Detailed description page of humcfs
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Humcfs_1561 details |
| Primary information | |
|---|---|
| Humcfs Id | Humcfs_1561 |
| chromosome_number | chromosome5 |
| name | FRA5G |
| chrlocation | 168500001-180915260 |
| cytoband | 5q35 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000131183 |
| gene_name | SLC34A1 |
| havana_transcript_id | OTTHUMT00000373165 |
| gene_location | 177379235-177386290 |
| gene_orientation | + |
| exon_id | ENSE00002051723, ENSE00003670450, ENSE00003531885, ENSE00002051908 |
| exon_number | 4 |
| gene_description | solute carrier family 34 (type II sodium/phosphate cotransporter), member 1 |
| disease_description | Idiopathic hypercalciuria,Reperfusion Injury,Acidosis,FANCONI RENOTUBULAR SYNDROME 2,Kidney Calculi,Hypercalcemia, Idiopathic, of Infancy,Nephrocalcinosis,Hypercalciuria,Tuberculosis, Pulmonary,Hypophosphatemia,Vitamin D-Resistant Rickets, X-Linked,Tuberculosis,Hypothyroidism,Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1,Hyperthyroidism,Kidney Diseases,Chronic Kidney Diseases,Kidney Failure, Chronic,Fanconi Syndrome,Polycystic Kidney, Autosomal Dominant,HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY,Nephrolithiasis,Hypercalcemia,Potassium Deficiency,Chronic Kidney Insufficiency,Bone Diseases, Developmental |
| miRNA_location | 168560904-168560926 |
| miRNA_strand | + |
| miRNA_id | MIMAT00074021 |
| miRNA_name | hsa-miR-103b |
| miRNA_derived | MI0007261 |
| Technique | Karyotyping |
| PMID | 15650228 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |