IpiRecord: IPI00288947

GO Annotation Table

Compiled GO Annotations (from IPI)

GO Term	Aspect	Human	Mouse	Rat
caveolar membrane	C			IDA
plasma membrane	C	TAS TAS		ISS
cytoplasm	C	TAS		ISS
heterotrimeric G-protein complex	C	NR	TAS TAS	TAS ISS ISS
caveola	C			IDA
guanyl nucleotide binding	F	IEA	IEA
nucleotide binding	F	IEA	IEA	IEA
GTPase activity	F	TAS	TAS TAS	ISS ISS TAS
signal transducer activity	F	IEA	IEA IEA	IEA
GTP binding	F	IEA IEA	IEA IEA	IEA
G-protein coupled receptor protein signaling pathway	P	IEA	IMP	ISS IEA
anti-apoptosis	P			IMP
signal transduction	P	IEA	IEA IEA	IEA
heart development	P	IEA	IMP	ISS IEA
positive regulation of apoptosis	P			TAS
embryonic digit morphogenesis	P	IEA	IGI	ISS IEA
phospholipase C activation	P	TAS		ISS IMP
regulation of melanocyte differentiation	P	IEA	IMP	ISS IEA
protein amino acid ADP-ribosylation	P	IEA	RCA	ISS IEA
neuron remodeling	P	IEA	IMP	ISS IEA
G-protein signaling, coupled to IP3 second messenger (phospholipase C activating)	P			IMP
regulation of action potential	P	IEA	IMP	ISS IEA
G-protein signaling, adenylate cyclase activating pathway	P	IEA	IDA	ISS IEA
positive regulation of smooth muscle cell proliferation	P			IMP
negative regulation of potassium ion transport	P			IMP
skeletal development	P	IEA	IMP	ISS IEA
blood coagulation	P	TAS		ISS
glutamate signaling pathway	P	IEA	IMP	ISS IEA
dopamine receptor, phospholipase C activating pathway	P		IGI
pigmentation during development	P	IEA	IMP	ISS IEA

Cellular Component

Biological Process

Molecular Function

Phenotype (22)

Compiled Mammalian Phenotype Ontology Annotations (from IPI)

MP Term	Aspect	Human	Mouse	Rat
skin/coat/nails phenotype	MP		Un
craniofacial phenotype	MP		Un Un
pigmentation phenotype	MP		Un
behavior/neurological phenotype	MP		Un Un
homeostasis/metabolism phenotype	MP		Un Un
lethality-embryonic/perinatal	MP		Un Un
skeleton phenotype	MP		Un
muscle phenotype	MP		Un
life span-post-weaning/aging	MP		Un
nervous system phenotype	MP		Un
growth/size phenotype	MP		Un
hematopoietic system phenotype	MP		Un Un
respiratory system phenotype	MP		Un
cardiovascular system phenotype	MP		Un Un
normal phenotype	MP		Un
limbs/digits/tail phenotype	MP		Un
hearing/vestibular/ear phenotype	MP		Un Un
touch/vibrissae phenotype	MP		Un
abnormal cardiovascular system morphology	N			ISS
embryonic lethality	N			ISS
abnormal craniofacial morphology	N			ISS
perinatal lethality	N			ISS

Disease (2)

Compiled Disease Ontology Annotations (from IPI)

DO Term	Aspect	Human	Mouse	Rat
Cardiomegaly	D			ISS
Cardiomyopathy, Congestive	D			ISS

Pathway (3)

Compiled Pathway Ontology Annotations (from IPI)

PW Term	Aspect	Human	Mouse	Rat
G protein signaling pathway via Galphaq family	W			IMP
orexin/hypocretin signaling pathway through the orexin/hypocretin receptor 1	W			IMP
orexin/hypocretin signaling pathway through the orexin/hypocretin receptor 2	W			IMP

KEGG Pathway (5)

KEGG Pathways for this protein (from IPI)

KEGG Pathway	Human	Mouse	Rat
GnRH signaling pathway (04912)	Present in KEGG pathway	Present in KEGG pathway	Present in KEGG pathway
Long-term depression (04730)	Present in KEGG pathway	Present in KEGG pathway	Present in KEGG pathway
Calcium signaling pathway (04020)	Present in KEGG pathway	Present in KEGG pathway	Present in KEGG pathway
Gap junction (04540)	Present in KEGG pathway	Present in KEGG pathway	Present in KEGG pathway
Long-term potentiation (04720)	Present in KEGG pathway	Present in KEGG pathway	Present in KEGG pathway