Detailed description page of humcfs

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Humcfs_2102 details
Primary information
Humcfs IdHumcfs_2102
chromosome_numberchromosome7
nameFRA7F
chrlocation98000001-107400000
cytoband7q22
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000170615
gene_nameSLC26A5
havana_transcript_idOTTHUMT00000313872
gene_location103374266-103443194
gene_orientation-
exon_idENSE00003608496, ENSE00003595732, ENSE00003607475, ENSE00003711797, ENSE00003546806, ENSE00003524121, ENSE00003487897, ENSE00003606411, ENSE00003674395, ENSE00003573513, ENSE00003486426, ENSE000036109
exon_number18
gene_descriptionsolute carrier family 26 (anion exchanger), member 5
disease_descriptionDiastrophic 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_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID3290488
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank