| 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
|
|
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
|
|
IFT38
|
intraflagellar transport 38
|
|
IFT43
|
intraflagellar transport 43
|
|
IFT46
|
intraflagellar transport 46
|
|
IFT52
|
intraflagellar transport 52
|
|
IFT54
|
intraflagellar transport 54
|
|
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
|
|
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
|
