midline defect of the nose Gene Set
Genes
14 genes associated with the midline defect of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ALX4
|
ALX homeobox 4
|
|
BCOR
|
BCL6 corepressor
|
|
EFNB1
|
ephrin-B1
|
|
FAM58A
|
family with sequence similarity 58, member A
|
|
FRAS1
|
Fraser extracellular matrix complex subunit 1
|
|
FREM1
|
FRAS1 related extracellular matrix 1
|
|
FREM2
|
FRAS1 related extracellular matrix protein 2
|
|
GRIP1
|
glutamate receptor interacting protein 1
|
|
HYLS1
|
hydrolethalus syndrome 1
|
|
NF1
|
neurofibromin 1
|
|
PTCH1
|
patched 1
|
|
TBX2
|
T-box 2
|
|
TBX4
|
T-box 4
|
|
ZSWIM6
|
zinc finger, SWIM-type containing 6
|
