Detailed description page of humcfs
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Humcfs_2965 details |
| Primary information | |
|---|---|
| Humcfs Id | Humcfs_2965 |
| chromosome_number | chromosome11 |
| name | FRA11B |
| chrlocation | 114500001-121200000 |
| cytoband | 11q23.3 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000149573 |
| gene_name | MPZL2 |
| havana_transcript_id | OTTHUMT00000392116 |
| gene_location | 118256911-118264536 |
| gene_orientation | - |
| exon_id | ENSE00001800629, ENSE00003529254, ENSE00003467285, ENSE00003653516, ENSE00002200582 |
| exon_number | 5 |
| gene_description | myelin protein zero-like 2 |
| disease_description | Pheochromocytoma,Dementia,Goiter,Coronary Arteriosclerosis,Sensorineural Hearing Loss (disorder),Presenile dementia,Impaired cognition,Enlarged Vestibular Aqueduct,Brain Infarction,Pendred's syndrome,Hypothyroidism,Hearing Loss, Mixed Conductive-Sensorineural,Congenital ear anomaly NOS (disorder),Malignant neoplasm of breast,Breast Carcinoma,Coronary heart disease |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | FISH |
| PMID | 17063465 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |