abnormality of the peritoneum Gene Set
Genes
17 genes associated with the abnormality of the peritoneum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
BCL2
|
B-cell CLL/lymphoma 2
|
|
BCL6
|
B-cell CLL/lymphoma 6
|
|
BRCA1
|
breast cancer 1, early onset
|
|
COL1A1
|
collagen, type I, alpha 1
|
|
COL5A1
|
collagen, type V, alpha 1
|
|
COL5A2
|
collagen, type V, alpha 2
|
|
EWSR1
|
EWS RNA-binding protein 1
|
|
F5
|
coagulation factor V (proaccelerin, labile factor)
|
|
HLA-DRB1
|
major histocompatibility complex, class II, DR beta 1
|
|
IKBKAP
|
inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
|
|
JAK2
|
Janus kinase 2
|
|
MEFV
|
Mediterranean fever
|
|
MVK
|
mevalonate kinase
|
|
SLC29A3
|
solute carrier family 29 (equilibrative nucleoside transporter), member 3
|
|
SOX18
|
SRY (sex determining region Y)-box 18
|
|
TNFRSF1A
|
tumor necrosis factor receptor superfamily, member 1A
|
|
WT1
|
Wilms tumor 1
|
