Primary information |
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Humcfs Id | Humcfs_2102 |
chromosome_number | chromosome7 |
name | FRA7F |
chrlocation | 98000001-107400000 |
cytoband | 7q22 |
type | Aphidicolin |
frequency | Common |
gene_ensembl_id | ENSG00000170615 |
gene_name | SLC26A5 |
havana_transcript_id | OTTHUMT00000313872 |
gene_location | 103374266-103443194 |
gene_orientation | - |
exon_id | ENSE00003608496, ENSE00003595732, ENSE00003607475, ENSE00003711797, ENSE00003546806, ENSE00003524121, ENSE00003487897, ENSE00003606411, ENSE00003674395, ENSE00003573513, ENSE00003486426, ENSE000036109 |
exon_number | 18 |
gene_description | solute carrier family 26 (anion exchanger), member 5 |
disease_description | Diastrophic dysplasia,Multiple Epiphyseal Dysplasia,Chondrodysplasia,DEAFNESS, AUTOSOMAL RECESSIVE 61,Deafness,Presbycusis,hearing impairment,Hearing Loss,Hypothyroidism,Hearing Loss, Partial,Hepatitis B,Hearing Loss, Mixed Conductive-Sensorineural |
miRNA_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | Karyotyping |
PMID | 3290488 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |