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Response to external stimulus
ACVRL1
: activin A receptor type II-like 1
ADAMTS13
: ADAM metallopeptidase with thrombospondin type 1 motif, 13
ALPL
: alkaline phosphatase, liver/bone/kidney
APOE
: apolipoprotein E
ATG16L1
: ATG16 autophagy related 16-like 1 (S. cerevisiae)
CACNA1F
: calcium channel, voltage-dependent, L type, alpha 1F subunit
CD40LG
: CD40 ligand
CLN3
: ceroid-lipofuscinosis, neuronal 3
COL11A1
: collagen, type XI, alpha 1
COL3A1
: collagen, type III, alpha 1
COL5A1
: collagen, type V, alpha 1
DRD3
: dopamine receptor D3
EDN3
: endothelin 3
EDNRB
: endothelin receptor type B
ERBB2
: v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian)
F12
: coagulation factor XII (Hageman factor)
F2
: coagulation factor II (thrombin)
F5
: coagulation factor V (proaccelerin, labile factor)
F8
: coagulation factor VIII, procoagulant component
F9
: coagulation factor IX
GNAT2
: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
HRAS
: v-Ha-ras Harvey rat sarcoma viral oncogene homolog
IL1A
: interleukin 1, alpha
KAL1
: Kallmann syndrome 1 sequence
LYST
: lysosomal trafficking regulator
MAP2K1
: mitogen-activated protein kinase kinase 1
MEFV
: Mediterranean fever
NF1
: neurofibromin 1
NLRP12
: NLR family, pyrin domain containing 12
NLRP3
: NLR family, pyrin domain containing 3
NOD2
: nucleotide-binding oligomerization domain containing 2
NR4A2
: nuclear receptor subfamily 4, group A, member 2
OPN1SW
: opsin 1 (cone pigments), short-wave-sensitive
PCSK9
: proprotein convertase subtilisin/kexin type 9
PROC
: protein C (inactivator of coagulation factors Va and VIIIa)
PROK2
: prokineticin 2
PROS1
: protein S (alpha)
RPS19
: ribosomal protein S19
SAA1
: serum amyloid A1
SBDS
: Shwachman-Bodian-Diamond syndrome
SERPING1
: serpin peptidase inhibitor, clade G (C1 inhibitor), member 1
SOD1
: superoxide dismutase 1, soluble
TGFB1
: transforming growth factor, beta 1
TP53
: tumor protein p53
TSC2
: tuberous sclerosis 2
VWF
: von Willebrand factor
WAS
: Wiskott-Aldrich syndrome (eczema-thrombocytopenia)
Source:
Gene Ontology
Consortium
(June 2009).
Published: November 20, 2009