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Details of FERMT3 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| FERMT3 | KIND3,MIG2B,URP2 | Q86UX7 | URP2_HUMAN | 83706
| ENSG00000149781
| Fermitin family homolog 3 | SPROT |
Disease |
|---|
| Disease |
OMIM id |
| Leukocyte adhesion deficiency 3 (LAD3) [MIM:612840]: A disorder characterized by recurrent bacterial infections without pus formation, leukocytosis and major bleeding disorders. Note=The disease is caused by mutations affecting the gene represented in this entry. |
612840 |
