Detailed description page of humcfs
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SH3PXD2B details |
| Primary information | |
|---|---|
| gene_name | SH3PXD2B |
| Humcfs Id | Humcfs_1625 |
| chromosome_number | chromosome5 |
| name | FRA5G |
| chrlocation | 168500001-180915260 |
| cytoband | 5q35 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000174705 |
| havana_transcript_id | OTTHUMT00000489226 |
| gene_location | 172325000-172454308 |
| gene_orientation | - |
| exon_id | ENSE00003799906, ENSE00001387642, ENSE00001375110, ENSE00001364389, ENSE00001378384, ENSE00003800058, ENSE00001391665, ENSE00001381933, ENSE00001385663, ENSE00001384794, ENSE00001385545, ENSE000025270 |
| exon_number | 14 |
| gene_description | SH3 and PX domains 2B |
| disease_description | Congenital Heart Defects,Infectious Otitis Media,Malignant tumor of colon,Secondary malignant neoplasm of lung,Otitis Media,Borrone Di Rocco Crovato syndrome,Eye Abnormalities,hearing impairment,Skeletal dysplasia,Ter Haar syndrome,Tobacco Use Disorder,OTITIS MEDIA, SUSCEPTIBILITY TO (finding),Growth Disorders,Colon Carcinoma,Obesity,Craniofacial Abnormalities,Bone Diseases, Developmental |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | Karyotyping |
| PMID | 15650228 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |