primary cilium Gene Set

Dataset GO Cellular Component Annotations
Category structural or functional annotations
Type cellular component
Description A cilium found on many different cell types that is typically present in a single copy per cell. A primary cilium may have a variable array of axonemal microtubules and may or may not contain molecular motors. (Gene Ontology, GO_0072372)
External Link http://amigo.geneontology.org/amigo/term/GO:0072372
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Genes

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

Symbol Name
ADCY5 adenylate cyclase 5
ADRBK1 adrenergic, beta, receptor kinase 1
AHI1 Abelson helper integration site 1
ANO2 anoctamin 2, calcium activated chloride channel
ARL13B ADP-ribosylation factor-like 13B
ARL2 ADP-ribosylation factor-like 2
ARL3 ADP-ribosylation factor-like 3
ARL6 ADP-ribosylation factor-like 6
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
CEP41 centrosomal protein 41kDa
CEP89 centrosomal protein 89kDa
CETN1 centrin, EF-hand protein, 1
CETN2 centrin, EF-hand protein, 2
CFAP126 cilia and flagella associated protein 126
CLUAP1 clusterin associated protein 1
CNGB3 cyclic nucleotide gated channel beta 3
CSNK1A1 casein kinase 1, alpha 1
CYS1 cystin 1
DCDC2 doublecortin domain containing 2
DFNB31 deafness, autosomal recessive 31
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1
DYNLL1 dynein, light chain, LC8-type 1
DYNLL2 dynein, light chain, LC8-type 2
DYNLRB1 dynein, light chain, roadblock-type 1
DYNLRB2 dynein, light chain, roadblock-type 2
EFCAB7 EF-hand calcium binding domain 7
ELMOD3 ELMO/CED-12 domain containing 3
FAM161A family with sequence similarity 161, member A
GLI1 GLI family zinc finger 1
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
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
GPR161 G protein-coupled receptor 161
GPR83 G protein-coupled receptor 83
GRXCR1 glutaredoxin, cysteine rich 1
HSPB11 heat shock protein family B (small), member 11
IFT122 intraflagellar transport 122
IFT140 intraflagellar transport 140
IFT172 intraflagellar transport 172
IFT20 intraflagellar transport 20
IFT22 intraflagellar transport 22
IFT27 intraflagellar transport 27
IFT43 intraflagellar transport 43
IFT46 intraflagellar transport 46
IFT52 intraflagellar transport 52
IFT57 intraflagellar transport 57
IFT74 intraflagellar transport 74
IFT80 intraflagellar transport 80
IFT81 intraflagellar transport 81
IFT88 intraflagellar transport 88
INHA inhibin, alpha
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
IQCB1 IQ motif containing B1
IQCE IQ motif containing E
KIF17 kinesin family member 17
KIF3A kinesin family member 3A
KIF3B kinesin family member 3B
KIF3C kinesin family member 3C
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
NEK8 NIMA-related kinase 8
NPHP1 nephronophthisis 1 (juvenile)
NPHP3 nephronophthisis 3 (adolescent)
NPHP4 nephronophthisis 4
NPY2R neuropeptide Y receptor Y2
OCRL oculocerebrorenal syndrome of Lowe
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PCDH15 protocadherin-related 15
PCM1 pericentriolar material 1
PDC phosducin
PDE4C phosphodiesterase 4C, cAMP-specific
PDE6D phosphodiesterase 6D, cGMP-specific, rod, delta
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKD1L1 polycystic kidney disease 1 like 1
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKD2L1 polycystic kidney disease 2-like 1
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
PPEF2 protein phosphatase, EF-hand calcium binding domain 2
PRKCA protein kinase C, alpha
PROM1 prominin 1
PTCH1 patched 1
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
PTPRK protein tyrosine phosphatase, receptor type, K
RAB10 RAB10, member RAS oncogene family
RAB14 RAB14, member RAS oncogene family
RAB15 RAB15, member RAS oncogene family
RAB27A RAB27A, member RAS oncogene family
RAB8A RAB8A, member RAS oncogene family
RHO rhodopsin
RILPL1 Rab interacting lysosomal protein-like 1
RILPL2 Rab interacting lysosomal protein-like 2
RP1 retinitis pigmentosa 1 (autosomal dominant)
RP2 retinitis pigmentosa 2 (X-linked recessive)
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
SMO smoothened, frizzled class receptor
SPA17 sperm autoantigenic protein 17
SPATA7 spermatogenesis associated 7
SPTBN5 spectrin, beta, non-erythrocytic 5
SSTR3 somatostatin receptor 3
STRC stereocilin
SUFU suppressor of fused homolog (Drosophila)
TBC1D30 TBC1 domain family, member 30
TBCC tubulin folding cofactor C
TNPO1 transportin 1
TOPORS topoisomerase I binding, arginine/serine-rich, E3 ubiquitin protein ligase
TRAF3IP1 TNF receptor-associated factor 3 interacting protein 1
TTC21B tetratricopeptide repeat domain 21B
TTC26 tetratricopeptide repeat domain 26
TTC30B tetratricopeptide repeat domain 30B
TTC8 tetratricopeptide repeat domain 8
TUBG1 tubulin, gamma 1
TULP1 tubby like protein 1
TULP3 tubby like protein 3
UMOD uromodulin
UNC119B unc-119 homolog B (C. elegans)
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH2A Usher syndrome 2A (autosomal recessive, mild)
WDR19 WD repeat domain 19
WDR34 WD repeat domain 34
WDR35 WD repeat domain 35
WDR60 WD repeat domain 60