| Primary information |
|---|
| Humcfs Id | Humcfs_2153 |
| chromosome_number | chromosome7 |
| name | FRA7H |
| chrlocation | 130400001-132600000 |
| cytoband | 7p32.3 |
| type | Aphidicolin |
| frequency | Common |
| gene_ensembl_id | ENSG00000106477 |
| gene_name | CEP41 |
| havana_transcript_id | OTTHUMT00000349754 |
| gene_location | 130400780-130426730 |
| gene_orientation | - |
| exon_id | ENSE00001915186, ENSE00003649764, ENSE00003693689, ENSE00001039832, ENSE00003649520, ENSE00003557671, ENSE00003662621, ENSE00001885059 |
| exon_number | 8 |
| gene_description | centrosomal protein 41kDa |
| disease_description | Child Development Disorders, Pervasive,Autism Spectrum Disorders,Familial aplasia of the vermis,JOUBERT SYNDROME 15 |
| miRNA_location | 130876748-130876769 |
| miRNA_strand | - |
| miRNA_id | MIMAT0000086 |
| miRNA_name | hsa-miR-29a-3p |
| miRNA_derived | MI0000087 |
| Technique | FISH |
| PMID | 9653154 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |