Entity Details
Details
| PrimaryID | 2165 |
| RefseqGene | NG_012065 |
| Symbol | F13B |
| Name | coagulation factor XIII B chain |
| Chromosome | 1 |
| Location | 1q31.3 |
| TaxID | 9606 |
| Status | live |
| SourceGenome | genomic |
| SourceOrigin | natural |
| CreationDate | 1998-08-13 |
| ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
| Disease ID | Source | Name | Description |
| 613235 | OMIM | Factor XIII subunit B deficiency (FA13BD) | An autosomal recessive hematologic disorder characterized by a life-long bleeding tendency, impaired wound healing and spontaneous abortion in affected women. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
9 interactions