Detailed description page of humcfs
| This page displays user query in tabular form. |
ESPN details |
| Primary information | |
|---|---|
| gene_name | ESPN |
| Humcfs Id | Humcfs_4 |
| chromosome_number | chromosome1 |
| name | FRA1A |
| chrlocation | 1-28000000 |
| cytoband | 1p36 |
| type | Aphidicolin |
| frequency | Common |
| gene_ensembl_id | ENSG00000187017 |
| havana_transcript_id | OTTHUMT00000001930 |
| gene_location | 6448467-6460052 |
| gene_orientation | + |
| exon_id | ENSE00001935497, ENSE00003576066, ENSE00003782259, ENSE00003610124, ENSE00003630784, ENSE00003685596, ENSE00001858371 |
| exon_number | 7 |
| gene_description | espin |
| disease_description | Melanocytic nevus,Nonsyndromic Deafness,melanoma,Retinal Degeneration,DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT,Deafness,DEAFNESS, AUTOSOMAL RECESSIVE (disorder),hearing impairment,Vestibular Diseases,Deafness, Autosomal Recessive 36, Without Vestibular Involvement,Usher Syndrome, Type II,Usher Syndrome,Hearing Loss, Mixed Conductive-Sensorineural |
| miRNA_location | 23057880-23057896 |
| miRNA_strand | - |
| miRNA_id | MIMAT0018931 |
| miRNA_name | hsa-miR-4419a |
| miRNA_derived | MI0016755 |
| Technique | Karyotyping |
| PMID | 1322577 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |