Laron Syndrome Gene Set
Genes
18 genes associated with the disease Laron Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
BCL2
|
B-cell CLL/lymphoma 2
|
|
CASP3
|
caspase 3, apoptosis-related cysteine peptidase
|
|
CASP9
|
caspase 9, apoptosis-related cysteine peptidase
|
|
DESI1
|
desumoylating isopeptidase 1
|
|
EGF
|
epidermal growth factor
|
|
GH1
|
growth hormone 1
|
|
GHR
|
growth hormone receptor
|
|
GHRHR
|
growth hormone releasing hormone receptor
|
|
IGF1
|
insulin-like growth factor 1 (somatomedin C)
|
|
IGFBP3
|
insulin-like growth factor binding protein 3
|
|
OPA1
|
optic atrophy 1 (autosomal dominant)
|
|
PROP1
|
PROP paired-like homeobox 1
|
|
SLC35G1
|
solute carrier family 35, member G1
|
|
SOAT1
|
sterol O-acyltransferase 1
|
|
STAT5A
|
signal transducer and activator of transcription 5A
|
|
STAT5B
|
signal transducer and activator of transcription 5B
|
|
TGM2
|
transglutaminase 2
|
|
TXNIP
|
thioredoxin interacting protein
|
