Robinow Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities. (Human Disease Ontology, DOID_0060254)
External Link https://www.disgenet.org/browser/0/1/0/C0265205
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Genes

21 genes associated with the disease Robinow Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ATR ATR serine/threonine kinase
CENPJ centromere protein J
CEP63 centrosomal protein 63kDa
DNAAF4 dynein axonemal assembly factor 4
DVL1 dishevelled segment polarity protein 1
DVL3 dishevelled segment polarity protein 3
FZD2 frizzled class receptor 2
GH1 growth hormone 1
IGF1 insulin-like growth factor 1 (somatomedin C)
KRAS Kirsten rat sarcoma viral oncogene homolog
LZTR1 leucine-zipper-like transcription regulator 1
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PRICKLE1 prickle homolog 1 (Drosophila)
PTCH1 patched 1
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RIT1 Ras-like without CAAX 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
SOS1 son of sevenless homolog 1 (Drosophila)
SYK spleen tyrosine kinase
WNT5A wingless-type MMTV integration site family, member 5A