preaxial polydactyly Gene Set
Genes
26 gene mutations causing the preaxial polydactyly phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ALX4
|
ALX homeobox 4
|
|
B9D1
|
B9 protein domain 1
|
|
BMP4
|
bone morphogenetic protein 4
|
|
CC2D2A
|
coiled-coil and C2 domain containing 2A
|
|
DPH1
|
diphthamide biosynthesis 1
|
|
EFNB1
|
ephrin-B1
|
|
FRAS1
|
Fraser extracellular matrix complex subunit 1
|
|
GLI3
|
GLI family zinc finger 3
|
|
HSPB11
|
heat shock protein family B (small), member 11
|
|
IFT122
|
intraflagellar transport 122
|
|
IFT172
|
intraflagellar transport 172
|
|
IFT80
|
intraflagellar transport 80
|
|
IFT88
|
intraflagellar transport 88
|
|
KIF7
|
kinesin family member 7
|
|
MEGF8
|
multiple EGF-like-domains 8
|
|
MKS1
|
Meckel syndrome, type 1
|
|
PAX9
|
paired box 9
|
|
PTCH1
|
patched 1
|
|
PTK7
|
protein tyrosine kinase 7 (inactive)
|
|
RECQL4
|
RecQ protein-like 4
|
|
RPGRIP1L
|
RPGRIP1-like
|
|
SDCCAG8
|
serologically defined colon cancer antigen 8
|
|
TBC1D32
|
TBC1 domain family, member 32
|
|
TCTN1
|
tectonic family member 1
|
|
TCTN2
|
tectonic family member 2
|
|
TMEM107
|
transmembrane protein 107
|
