abnormal rostral-caudal body axis extension Gene Set
Genes
14 gene mutations causing the abnormal rostral-caudal body axis extension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Symbol |
Name |
C2CD3
|
C2 calcium-dependent domain containing 3
|
CYFIP1
|
cytoplasmic FMR1 interacting protein 1
|
EPB41L5
|
erythrocyte membrane protein band 4.1 like 5
|
FGFR1
|
fibroblast growth factor receptor 1
|
MLLT4
|
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 4
|
NCSTN
|
nicastrin
|
PDPK1
|
3-phosphoinositide dependent protein kinase 1
|
PHACTR4
|
phosphatase and actin regulator 4
|
PTPN12
|
protein tyrosine phosphatase, non-receptor type 12
|
RAC1
|
ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)
|
RDH10
|
retinol dehydrogenase 10 (all-trans)
|
SALL4
|
spalt-like transcription factor 4
|
SOX9
|
SRY (sex determining region Y)-box 9
|
YAP1
|
Yes-associated protein 1
|