Genes associated with “SSTR2”
How are genes scored? (0–100 composite)
Strong Candidates
4 genesConsider
716 genesBRCA1 DNA repair associated
menin 1
von Hippel-Lindau tumor suppressor
transmembrane protein 127
cyclin dependent kinase inhibitor 1B
succinate dehydrogenase complex subunit D
catenin beta 1
somatostatin receptor 5
somatostatin receptor 1
somatostatin receptor 3
CREB binding lysine acetyltransferase
phosphatase and tensin homolog
ATRX chromatin remodeler
lysine methyltransferase 2D
ATM serine/threonine kinase
HNF1 homeobox A
AT-rich interaction domain 1A
BCL6 corepressor
serine/threonine kinase 11
EP300 lysine acetyltransferase
patched 1
SMAD family member 4
lysine methyltransferase 2A
bromodomain containing 4
ERCC excision repair 5, endonuclease
RB transcriptional corepressor 1
APC regulator of Wnt signaling pathway
KRAS proto-oncogene, GTPase
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
KIT proto-oncogene, receptor tyrosine kinase
interferon alpha and beta receptor subunit 1
kinase insert domain receptor
notch receptor 1
B-Raf proto-oncogene, serine/threonine kinase
TSC complex subunit 2
FAT atypical cadherin 4
BRCA2 DNA repair associated
Possible
462 genes — click to expand
somatostatin receptor 4
FAT atypical cadherin 1
Corneal dystrophy, Fuchs endothelial, 3
tryptophan hydroxylase 1
erb-b2 receptor tyrosine kinase 4
tryptophan hydroxylase 2
interferon alpha and beta receptor subunit 2
zinc finger homeobox 3
NUT midline carcinoma family member 1
LDL receptor related protein 1B
SH3 AND MULTIPLE ANKYRIN REPEAT DOMAINS 1; SHANK1
Intellectual developmental disorder, autosomal dominant 43
Related phenotype searches
Data aggregated from HPO/Monarch, ClinVar, OMIM (phenotypes + clinical synopsis), Open Targets, PanelApp, Phen2Gene, and Gene2Phenotype. Click a gene to view full details.