nonmotile primary cilium Gene Set

Dataset GO Cellular Component Annotations
Category structural or functional annotations
Type cellular component
Description A primary cilium which contains a variable array of axonemal microtubules but does not contain molecular motors. Nonmotile primary cilia are found on many different cell types and function as sensory organelles that concentrate and organize sensory signaling molecules. (Gene Ontology, GO_0031513)
External Link http://amigo.geneontology.org/amigo/term/GO:0031513
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Genes

74 proteins localized to the nonmotile primary cilium cellular component from the curated GO Cellular Component Annotations dataset.

Symbol Name
AHI1 Abelson helper integration site 1
ANO2 anoctamin 2, calcium activated chloride channel
ARL3 ADP-ribosylation factor-like 3
ARR3 arrestin 3, retinal (X-arrestin)
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
BBS4 Bardet-Biedl syndrome 4
C2ORF71 chromosome 2 open reading frame 71
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CEP290 centrosomal protein 290kDa
CEP89 centrosomal protein 89kDa
CETN1 centrin, EF-hand protein, 1
CETN2 centrin, EF-hand protein, 2
CNGB3 cyclic nucleotide gated channel beta 3
DFNB31 deafness, autosomal recessive 31
ELMOD3 ELMO/CED-12 domain containing 3
FAM161A family with sequence similarity 161, member A
GNAT1 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1
GNAT2 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
GNAT3 guanine nucleotide binding protein, alpha transducing 3
GPR83 G protein-coupled receptor 83
GRXCR1 glutaredoxin, cysteine rich 1
IFT122 intraflagellar transport 122
IFT140 intraflagellar transport 140
IFT20 intraflagellar transport 20
IFT52 intraflagellar transport 52
IFT57 intraflagellar transport 57
IFT88 intraflagellar transport 88
INHA inhibin, alpha
IQCB1 IQ motif containing B1
KIF17 kinesin family member 17
KIFAP3 kinesin-associated protein 3
KNCN kinocilin
MAK male germ cell-associated kinase
MCHR1 melanin-concentrating hormone receptor 1
MERTK MER proto-oncogene, tyrosine kinase
MYO3B myosin IIIB
MYO5A myosin VA (heavy chain 12, myoxin)
MYO7A myosin VIIA
MYRIP myosin VIIA and Rab interacting protein
NPHP1 nephronophthisis 1 (juvenile)
NPHP4 nephronophthisis 4
NPY2R neuropeptide Y receptor Y2
OCRL oculocerebrorenal syndrome of Lowe
PCDH15 protocadherin-related 15
PCM1 pericentriolar material 1
PDC phosducin
PKD1L1 polycystic kidney disease 1 like 1
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKD2L1 polycystic kidney disease 2-like 1
PPEF2 protein phosphatase, EF-hand calcium binding domain 2
PRKCA protein kinase C, alpha
PROM1 prominin 1
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
PTPRK protein tyrosine phosphatase, receptor type, K
RAB27A RAB27A, member RAS oncogene family
RAB8A RAB8A, member RAS oncogene family
RHO rhodopsin
RP1 retinitis pigmentosa 1 (autosomal dominant)
RPGR retinitis pigmentosa GTPase regulator
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
SAG S-antigen; retina and pineal gland (arrestin)
SHANK2 SH3 and multiple ankyrin repeat domains 2
SPATA7 spermatogenesis associated 7
SPTBN5 spectrin, beta, non-erythrocytic 5
SSTR3 somatostatin receptor 3
STRC stereocilin
TBCC tubulin folding cofactor C
TOPORS topoisomerase I binding, arginine/serine-rich, E3 ubiquitin protein ligase
TTC8 tetratricopeptide repeat domain 8
TUBG1 tubulin, gamma 1
TULP1 tubby like protein 1
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH2A Usher syndrome 2A (autosomal recessive, mild)
WDR19 WD repeat domain 19