| Primary information |
|---|
| Humcfs Id | Humcfs_4856 |
| chromosome_number | chromosome19 |
| name | FRA19B |
| chrlocation | 1-20000000 |
| cytoband | 19p13 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000125656 |
| gene_name | CLPP |
| havana_transcript_id | OTTHUMT00000452988 |
| gene_location | 6361863-6368902 |
| gene_orientation | + |
| exon_id | ENSE00003102007, ENSE00003540033, ENSE00003586054, ENSE00003207626 |
| exon_number | 4 |
| gene_description | caseinolytic mitochondrial matrix peptidase proteolytic subunit |
| disease_description | Gonadal dysgenesis XX type deafness,Nonsyndromic Deafness,PERRAULT SYNDROME 3 |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | FISH |
| PMID | 3568428 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |