Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionG protein-coupled photoreceptor activity

OPN1LW OPN1MW OPN1MW2 OPN1MW3

6.30e-0715954GO:0008020
GeneOntologyMolecularFunctionphotoreceptor activity

OPN1LW OPN1MW OPN1MW2 OPN1MW3

1.09e-0617954GO:0009881
GeneOntologyMolecularFunctionL-serine-phosphatidylethanolamine phosphatidyltransferase activity

PTDSS1 PTDSS2

2.24e-052952GO:0106245
GeneOntologyMolecularFunctionmonoatomic cation transmembrane transporter activity

SLC4A8 TCIRG1 COX15 SLC13A3 GRIK2 SLC40A1 CALHM2 KCNF1 ATP6V0A4 SLC5A8 SLC30A9 ATP1A4

7.26e-056649512GO:0008324
GeneOntologyMolecularFunctionmonoatomic ion transmembrane transporter activity

BEST1 SLC4A8 TCIRG1 COX15 SLC13A3 GRIK2 SLC40A1 CALHM2 KCNF1 ATP6V0A4 SLC5A8 SLC30A9 ATP1A4

9.56e-057939513GO:0015075
GeneOntologyMolecularFunctiontransporter activity

ATP8B3 BEST1 SLC22A25 SLC4A8 TCIRG1 COX15 SLC13A3 GRIK2 SLC40A1 CALHM2 SLC50A1 KCNF1 ATP6V0A4 SLC5A8 RFT1 SLC30A9 ATP1A4

1.11e-0412899517GO:0005215
GeneOntologyMolecularFunctioninorganic cation transmembrane transporter activity

SLC4A8 TCIRG1 COX15 SLC13A3 GRIK2 SLC40A1 KCNF1 ATP6V0A4 SLC5A8 SLC30A9 ATP1A4

1.92e-046279511GO:0022890
GeneOntologyMolecularFunctionNADPH oxidase H202-forming activity

MICAL1 DUOX2

2.22e-045952GO:0106294
GeneOntologyMolecularFunctionshort-chain fatty acid transmembrane transporter activity

SLC22A25 SLC5A8

2.22e-045952GO:0015636
GeneOntologyMolecularFunctioninorganic molecular entity transmembrane transporter activity

BEST1 SLC4A8 TCIRG1 COX15 SLC13A3 GRIK2 SLC40A1 KCNF1 ATP6V0A4 SLC5A8 SLC30A9 ATP1A4

2.50e-047589512GO:0015318
GeneOntologyMolecularFunctionG protein-coupled receptor activity

OR5D16 CCR10 FFAR3 OPN1LW OPN1MW BDKRB2 OR1D2 OPN1MW2 GHSR OPN1MW3 TAS2R5 OR52N4 HCRTR2

2.78e-048849513GO:0004930
GeneOntologyMolecularFunctiontransmembrane transporter activity

BEST1 SLC22A25 SLC4A8 TCIRG1 COX15 SLC13A3 GRIK2 SLC40A1 CALHM2 SLC50A1 KCNF1 ATP6V0A4 SLC5A8 SLC30A9 ATP1A4

4.38e-0411809515GO:0022857
GeneOntologyMolecularFunctionactive transmembrane transporter activity

SLC22A25 SLC4A8 TCIRG1 COX15 SLC13A3 ATP6V0A4 SLC5A8 SLC30A9 ATP1A4

4.48e-04477959GO:0022804
GeneOntologyMolecularFunctionactive monoatomic ion transmembrane transporter activity

SLC4A8 TCIRG1 COX15 SLC13A3 ATP6V0A4 SLC5A8 ATP1A4

5.88e-04301957GO:0022853
GeneOntologyMolecularFunctiontransmembrane signaling receptor activity

OR5D16 CCR10 FFAR3 OPN1LW GRIK2 OPN1MW BDKRB2 OR1D2 OPN1MW2 GHSR OPN1MW3 TAS2R5 OR52N4 FCRL5 IL5RA HCRTR2

6.13e-0413539516GO:0004888
GeneOntologyMolecularFunctionsodium ion transmembrane transporter activity

SLC4A8 SLC13A3 GRIK2 SLC5A8 ATP1A4

1.35e-03171955GO:0015081
GeneOntologyMolecularFunctionNAD(P)H oxidase H2O2-forming activity

MICAL1 DUOX2

1.43e-0312952GO:0016174
GeneOntologyMolecularFunctionmetal ion transmembrane transporter activity

SLC4A8 SLC13A3 GRIK2 SLC40A1 KCNF1 SLC5A8 SLC30A9 ATP1A4

1.69e-03465958GO:0046873
GeneOntologyMolecularFunctionpeptide hormone binding

SLC40A1 GHSR HCRTR2

2.29e-0355953GO:0017046
GeneOntologyBiologicalProcessdetection of external stimulus

BEST1 OPN1LW PDZD7 GRIK2 OPN1MW OPN1MW2 OPN1MW3 PCDH15

1.36e-06173958GO:0009581
GeneOntologyBiologicalProcessdetection of abiotic stimulus

BEST1 OPN1LW PDZD7 GRIK2 OPN1MW OPN1MW2 OPN1MW3 PCDH15

1.48e-06175958GO:0009582
GeneOntologyBiologicalProcessdetection of visible light

BEST1 OPN1LW OPN1MW OPN1MW2 OPN1MW3

6.46e-0657955GO:0009584
GeneOntologyBiologicalProcessvisual perception

BEST1 MYO7A OPN1LW OPN1MW OPN1MW2 OPN1MW3 PCDH15 CLDN19

1.12e-05230958GO:0007601
GeneOntologyBiologicalProcesssensory perception of light stimulus

BEST1 MYO7A OPN1LW OPN1MW OPN1MW2 OPN1MW3 PCDH15 CLDN19

1.23e-05233958GO:0050953
GeneOntologyBiologicalProcessdetection of light stimulus

BEST1 OPN1LW OPN1MW OPN1MW2 OPN1MW3

2.83e-0577955GO:0009583
GeneOntologyBiologicalProcesssensory perception

OR5D16 BEST1 MYO7A LHFPL3 OPN1LW PDZD7 GRIK2 OPN1MW OR1D2 OPN1MW2 OPN1MW3 TAS2R5 ATP6V0A4 OR52N4 PCDH15 CLDN19

2.90e-0510729516GO:0007600
GeneOntologyBiologicalProcessphototransduction

OPN1LW OPN1MW OPN1MW2 OPN1MW3

1.04e-0453954GO:0007602
GeneOntologyBiologicalProcessdetection of stimulus

OR5D16 BEST1 OPN1LW PDZD7 GRIK2 OPN1MW OR1D2 OPN1MW2 OPN1MW3 TAS2R5 OR52N4 PCDH15

1.18e-047229512GO:0051606
GeneOntologyBiologicalProcessphosphatidylserine biosynthetic process

PTDSS1 PTDSS2

1.25e-044952GO:0006659
GeneOntologyBiologicalProcessauditory receptor cell stereocilium organization

MYO7A PDZD7 PCDH15

2.28e-0426953GO:0060088
GeneOntologyCellularComponentphotoreceptor outer segment

MYO7A OPN1LW OPN1MW OPN1MW2 OPN1MW3 PCDH15 ATP1A4

7.94e-07111967GO:0001750
GeneOntologyCellularComponentphotoreceptor cell cilium

MYO7A OPN1LW OPN1MW OPN1MW2 OPN1MW3 PCDH15 ATP1A4

3.60e-06139967GO:0097733
GeneOntologyCellularComponentphotoreceptor disc membrane

OPN1LW OPN1MW OPN1MW2 OPN1MW3

5.78e-0626964GO:0097381
GeneOntologyCellularComponent9+0 non-motile cilium

MYO7A OPN1LW OPN1MW OPN1MW2 OPN1MW3 PCDH15 ATP1A4

6.78e-06153967GO:0097731
GeneOntologyCellularComponentnon-motile cilium

MYO7A OPN1LW OPN1MW OPN1MW2 OPN1MW3 PCDH15 ATP1A4

3.37e-05196967GO:0097730
GeneOntologyCellularComponenthippocampal mossy fiber

MICAL1 SLC4A8

4.32e-047962GO:0097457
GeneOntologyCellularComponentstereocilia coupling link

MYO7A PDZD7

5.74e-048962GO:0002139
GeneOntologyCellularComponentbasolateral plasma membrane

BEST1 SLC22A25 SLC4A8 SLC13A3 SLC40A1 ATP6V0A4 CLDN19

6.87e-04320967GO:0016323
GeneOntologyCellularComponentvacuolar proton-transporting V-type ATPase, V0 domain

TCIRG1 ATP6V0A4

9.17e-0410962GO:0000220
GeneOntologyCellularComponentbasal plasma membrane

BEST1 SLC22A25 SLC4A8 SLC13A3 SLC40A1 ATP6V0A4 CLDN19

1.24e-03354967GO:0009925
GeneOntologyCellularComponentproton-transporting V-type ATPase, V0 domain

TCIRG1 ATP6V0A4

1.34e-0312962GO:0033179
GeneOntologyCellularComponentcation-transporting ATPase complex

TCIRG1 ATP6V0A4 ATP1A4

1.48e-0349963GO:0090533
GeneOntologyCellularComponentbasal part of cell

BEST1 SLC22A25 SLC4A8 SLC13A3 SLC40A1 ATP6V0A4 CLDN19

1.80e-03378967GO:0045178
GeneOntologyCellularComponentapical plasma membrane

RAPGEF6 SLC4A8 MYO7A TCIRG1 DUOX2 ATP6V0A4 PRKAA1 SLC5A8

1.81e-03487968GO:0016324
GeneOntologyCellularComponentATPase dependent transmembrane transport complex

TCIRG1 ATP6V0A4 ATP1A4

2.07e-0355963GO:0098533
HumanPhenoBlue cone monochromacy

OPN1LW OPN1MW

3.82e-052322HP:0007939
HumanPhenoCone monochromacy

OPN1LW OPN1MW

3.82e-052322HP:0011517
HumanPhenoReduced OCT-measured foveal thickness

OPN1LW OPN1MW

1.14e-043322HP:0030619
HumanPhenoBilateral basal ganglia lesions

COX15 RFT1

1.14e-043322HP:0007146
MousePhenodecreased b-wave amplitude

MYO7A OPN1LW OPN1MW2 OPN1MW3 PCDH15

6.31e-0582725MP:0012144
MousePhenoabnormal b-wave shape

MYO7A OPN1LW OPN1MW2 OPN1MW3 PCDH15

7.50e-0585725MP:0012035
MousePhenoabnormal b-wave amplitude

MYO7A OPN1LW OPN1MW2 OPN1MW3 PCDH15

7.50e-0585725MP:0012031
MousePhenodecreased outer hair cell stereocilia number

MYO7A PDZD7 PCDH15

1.01e-0418723MP:0004529
DomainOpsin_red/grn

OPN1LW OPN1MW OPN1MW3

1.12e-073913IPR000378
DomainOPSIN

OPN1LW OPN1MW OPN1MW3

1.31e-0510913PS00238
DomainOpsin

OPN1LW OPN1MW OPN1MW3

1.79e-0511913IPR001760
DomainPSS

PTDSS1 PTDSS2

2.35e-052912IPR004277
DomainPSS

PTDSS1 PTDSS2

2.35e-052912PF03034
DomainV-type_ATPase_116kDa_su_euka

TCIRG1 ATP6V0A4

1.40e-044912IPR026028
DomainV_ATPase_I

TCIRG1 ATP6V0A4

1.40e-044912PF01496
DomainV-ATPase_116kDa_su

TCIRG1 ATP6V0A4

1.40e-044912IPR002490
DomainGPCR_Rhodpsn_7TM

OR5D16 CCR10 FFAR3 OPN1LW OPN1MW BDKRB2 OR1D2 GHSR OPN1MW3 OR52N4 HCRTR2

4.07e-046709111IPR017452
Domain7tm_1

OR5D16 CCR10 FFAR3 OPN1LW OPN1MW BDKRB2 OR1D2 GHSR OPN1MW3 OR52N4 HCRTR2

4.44e-046779111PF00001
DomainG_PROTEIN_RECEP_F1_1

OR5D16 CCR10 FFAR3 OPN1LW OPN1MW BDKRB2 OR1D2 GHSR OPN1MW3 OR52N4 HCRTR2

4.90e-046859111PS00237
DomainF-box_dom

FBXW10B FBXW10 FBXO10 FBXO7

4.92e-0475914IPR001810
DomainG_PROTEIN_RECEP_F1_2

OR5D16 CCR10 FFAR3 OPN1LW OPN1MW BDKRB2 OR1D2 GHSR OPN1MW3 OR52N4 HCRTR2

5.27e-046919111PS50262
DomainGPCR_Rhodpsn

OR5D16 CCR10 FFAR3 OPN1LW OPN1MW BDKRB2 OR1D2 GHSR OPN1MW3 OR52N4 HCRTR2

5.34e-046929111IPR000276
Domainaa-tRNA-synth_I_CS

EPRS1 VARS1

3.41e-0318912IPR001412
DomainAA_TRNA_LIGASE_I

EPRS1 VARS1

3.80e-0319912PS00178
DomainClaudin_CS

CLDN22 CLDN19

5.09e-0322912IPR017974
DomainCLAUDIN

CLDN22 CLDN19

5.09e-0322912PS01346
DomainFBOX

FBXW10 FBXO10 FBXO7

5.24e-0372913PS50181
PathwayREACTOME_THE_RETINOID_CYCLE_IN_CONES_DAYLIGHT_VISION

OPN1LW OPN1MW2 OPN1MW3

6.45e-068703MM14880
PathwayREACTOME_OPSINS

OPN1LW OPN1MW2 OPN1MW3

1.37e-0510703MM15063
PathwayWP_GPCRS_CLASS_A_RHODOPSINLIKE

CCR10 FFAR3 OPN1LW OPN1MW BDKRB2 OR1D2 GHSR HCRTR2

4.23e-05260708M39397
Pubmed

Human L- and M-opsins restore M-cone function in a mouse model for human blue cone monochromacy.

OPN1LW OPN1MW OPN1MW2 OPN1MW3

5.68e-11497429386880
Pubmed

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.

OPN1LW OPN1MW OPN1MW2 OPN1MW3

2.84e-1059742937147
Pubmed

Molecular determinants of human red/green color discrimination.

OPN1LW OPN1MW OPN1MW2

2.10e-0839738185948
Pubmed

X-linked cone dystrophy caused by mutation of the red and green cone opsins.

OPN1LW OPN1MW OPN1MW2

2.10e-08397320579627
Pubmed

Expression of red/green-cone opsin mutants K82E, P187S, M273K result in unique pathobiological perturbations to cone structure and function.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397338410159
Pubmed

Chloride-dependent spectral tuning mechanism of L-group cone visual pigments.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397323350963
Pubmed

Distinct contributions of rod, cone, and melanopsin photoreceptors to encoding irradiance.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397320471354
Pubmed

Multiple hypothalamic cell populations encoding distinct visual information.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397321224225
Pubmed

Circadian Regulation of the Rod Contribution to Mesopic Vision in Mice.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397336216501
Pubmed

Spectral tuning of a circadian photopigment in a subterranean 'blind' mammal (Spalax ehrenbergi).

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397310567724
Pubmed

Extensive cone-dependent spectral opponency within a discrete zone of the lateral geniculate nucleus supporting mouse color vision.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397334111401
Pubmed

Genetically engineered mice with an additional class of cone photoreceptors: implications for the evolution of color vision.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397314500905
Pubmed

Gene-based Therapy in a Mouse Model of Blue Cone Monochromacy.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397328751656
Pubmed

Rescue of M-cone Function in Aged Opn1mw-/- Mice, a Model for Late-Stage Blue Cone Monochromacy.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397331469404
Pubmed

The molecular genetics and evolution of red and green color vision in vertebrates.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397311545071
Pubmed

Mechanisms of spectral tuning in the mouse green cone pigment.

OPN1LW OPN1MW2 OPN1MW3

2.10e-0839739238068
Pubmed

Emergence of novel color vision in mice engineered to express a human cone photopigment.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397317379811
Pubmed

Co-expression of murine opsins facilitates identifying the site of cone adaptation.

OPN1LW OPN1MW2 OPN1MW3

2.10e-08397312511072
Pubmed

The Pem homeobox gene is X-linked and exclusively expressed in extraembryonic tissues during early murine development.

OPN1LW OPN1MW2 OPN1MW3

2.10e-0839737958444
Pubmed

Visual responses in the dorsal lateral geniculate nucleus at early stages of retinal degeneration in rd1 PDE6β mice.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497331461375
Pubmed

Murine and bovine blue cone pigment genes: cloning and characterization of two new members of the S family of visual pigments.

OPN1LW OPN1MW2 OPN1MW3

8.40e-0849738088841
Pubmed

Modulation of Fast Narrowband Oscillations in the Mouse Retina and dLGN According to Background Light Intensity.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497328103478
Pubmed

Molecular biology of the visual pigments.

OPN1LW OPN1MW OPN1MW2

8.40e-0849733303660
Pubmed

Cones Support Alignment to an Inconsistent World by Suppressing Mouse Circadian Responses to the Blue Colors Associated with Twilight.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497331846668
Pubmed

Melanopsin-driven increases in maintained activity enhance thalamic visual response reliability across a simulated dawn.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497326438865
Pubmed

Light/dark translocation of alphatransducin in mouse photoreceptor cells expressing G90D mutant opsin.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497317249565
Pubmed

Structural and functional rescue of cones carrying the most common cone opsin C203R missense mutation.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497338060327
Pubmed

Contribution of M-opsin-based color vision to refractive development in mice.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497334126082
Pubmed

Physiological features of the S- and M-cone photoreceptors of wild-type mice from single-cell recordings.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497316567464
Pubmed

S-opsin knockout mice with the endogenous M-opsin gene replaced by an L-opsin variant.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497324801621
Pubmed

Melanopsin Contributions to the Representation of Images in the Early Visual System.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497328528909
Pubmed

Melanopsin-driven light adaptation in mouse vision.

OPN1LW OPN1MW2 OPN1MW3

8.40e-08497325308073
Pubmed

Noncoding Mutations in a Thyroid Hormone Receptor Gene That Impair Cone Photoreceptor Function.

OPN1LW OPN1MW2 OPN1MW3

2.09e-07597336631163
Pubmed

Using Silent Substitution to Track the Mesopic Transition From Rod- to Cone-Based Vision in Mice.

OPN1LW OPN1MW2 OPN1MW3

2.09e-07597326818794
Pubmed

A common integration locus in type B retrovirus-induced thymic lymphomas.

OPN1LW OPN1MW2 OPN1MW3

2.09e-0759731333116
Pubmed

A distinct contribution of short-wavelength-sensitive cones to light-evoked activity in the mouse pretectal olivary nucleus.

OPN1LW OPN1MW2 OPN1MW3

2.09e-07597322090509
Pubmed

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions.

OPN1LW OPN1MW2 OPN1MW3

2.09e-07597310723722
Pubmed

Peripherin-2 differentially interacts with cone opsins in outer segments of cone photoreceptors.

OPN1LW OPN1MW2 OPN1MW3

2.09e-07597327033727
Pubmed

Melanopsin-based brightness discrimination in mice and humans.

OPN1LW OPN1MW2 OPN1MW3

2.09e-07597322633808
Pubmed

The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning.

OPN1LW OPN1MW2 OPN1MW3

2.09e-07597311055434
Pubmed

Enhancer/promoter activities of the long/middle wavelength-sensitive opsins of vertebrates mediated by thyroid hormone receptor β2 and COUP-TFII.

OPN1LW OPN1MW2 OPN1MW3

2.09e-07597324058409
Pubmed

Variations in photoreceptor throughput to mouse visual cortex and the unique effects on tuning.

OPN1LW OPN1MW2 OPN1MW3

2.09e-07597334099749
Pubmed

Functional comparison of rod and cone Gα(t) on the regulation of light sensitivity.

OPN1LW OPN1MW2 OPN1MW3

4.18e-07697323288843
Pubmed

Reduced levels of dystrophin associated proteins in the brains of mice deficient for Dp71.

OPN1LW OPN1MW2 OPN1MW3

4.18e-0769738872469
Pubmed

A thyroid hormone receptor that is required for the development of green cone photoreceptors.

OPN1LW OPN1MW2 OPN1MW3

4.18e-07697311138006
Pubmed

Impaired cytokine signaling in mice lacking the IL-1 receptor-associated kinase.

OPN1LW OPN1MW2 OPN1MW3

4.18e-07697310395695
Pubmed

Transient expression of thyroid hormone nuclear receptor TRbeta2 sets S opsin patterning during cone photoreceptor genesis.

OPN1LW OPN1MW2 OPN1MW3

4.18e-07697317436273
Pubmed

Telomere-related markers for the pseudoautosomal region of the mouse genome.

OPN1LW OPN1MW2 OPN1MW3

4.18e-0769731549575
Pubmed

Retarded developmental expression and patterning of retinal cone opsins in hypothyroid mice.

OPN1LW OPN1MW2 OPN1MW3

7.30e-07797318974269
Pubmed

Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome.

OPN1LW OPN1MW2 OPN1MW3

7.30e-0779738001979
Pubmed

NeuroD1 regulates expression of thyroid hormone receptor 2 and cone opsins in the developing mouse retina.

OPN1LW OPN1MW2 OPN1MW3

7.30e-07797318199774
Pubmed

Mapping of the murine tbl1 gene reveals a new rearrangement between mouse and human X Chromosomes.

OPN1LW OPN1MW2 OPN1MW3

7.30e-0779739880679
Pubmed

Characterization of cDNAs encoding the murine interleukin 2 receptor (IL-2R) gamma chain: chromosomal mapping and tissue specificity of IL-2R gamma chain expression.

OPN1LW OPN1MW2 OPN1MW3

7.30e-0779738378320
Pubmed

Rod Photoreceptor Activation Alone Defines the Release of Dopamine in the Retina.

OPN1LW OPN1MW2 OPN1MW3

7.30e-07797330799247
Pubmed

Activation of the blue opsin gene in cone photoreceptor development by retinoid-related orphan receptor beta.

OPN1LW OPN1MW2 OPN1MW3

7.30e-07797316574740
Pubmed

Rods progressively escape saturation to drive visual responses in daylight conditions.

OPN1LW OPN1MW2 OPN1MW3

7.30e-07797329180667
Pubmed

Cloning and distribution of myosin 3B in the mouse retina: differential distribution in cone outer segments.

OPN1LW OPN1MW2 OPN1MW3

7.30e-07797319332056
Pubmed

Localization of the mdx mutation within the mouse dystrophin gene.

OPN1LW OPN1MW2 OPN1MW3

1.17e-0689732903046
Pubmed

Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromes.

OPN1LW OPN1MW2 OPN1MW3

1.17e-0689731572654
Pubmed

Two transcription factors can direct three photoreceptor outcomes from rod precursor cells in mouse retinal development.

OPN1LW OPN1MW2 OPN1MW3

1.17e-06897321813673
Pubmed

X-chromosome gene order in different Mus species crosses.

OPN1LW OPN1MW2 OPN1MW3

1.17e-0689733416629
Pubmed

The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis.

OPN1LW OPN1MW2 OPN1MW3

1.17e-06897312651948
Pubmed

Transcriptional profiling of murine retinas undergoing semi-synchronous cone photoreceptor differentiation.

OPN1LW OPN1MW2 OPN1MW3

1.17e-06897331163126
Pubmed

Type 3 deiodinase, a thyroid-hormone-inactivating enzyme, controls survival and maturation of cone photoreceptors.

OPN1LW OPN1MW2 OPN1MW3

1.17e-06897320203194
Pubmed

Tubby is required for trafficking G protein-coupled receptors to neuronal cilia.

OPN1LW OPN1MW2 OPN1MW3

1.17e-06897323351594
Pubmed

A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3).

OPN1LW OPN1MW2 OPN1MW3

1.17e-06897310725384
Pubmed

Retinoid X receptor (gamma) is necessary to establish the S-opsin gradient in cone photoreceptors of the developing mouse retina.

OPN1LW OPN1MW2 OPN1MW3

1.17e-06897316043864
Pubmed

Nr2e3 functional domain ablation by CRISPR-Cas9D10A identifies a new isoform and generates retinitis pigmentosa and enhanced S-cone syndrome models.

OPN1LW OPN1MW2 OPN1MW3

1.17e-06897333007388
Pubmed

Linkage of amelogenin (Amel) to the distal portion of the mouse X chromosome.

OPN1LW OPN1MW2 OPN1MW3

1.17e-0689731675194
Pubmed

Retinal dystrophy resulting from ablation of RXR alpha in the mouse retinal pigment epithelium.

OPN1LW OPN1MW2 OPN1MW3

1.75e-06997314742273
Pubmed

Feedback induction of a photoreceptor-specific isoform of retinoid-related orphan nuclear receptor β by the rod transcription factor NRL.

OPN1LW OPN1MW2 OPN1MW3

1.75e-06997325296752
Pubmed

Comparative mapping of the actin-binding protein 280 genes in human and mouse.

OPN1LW OPN1MW2 OPN1MW3

1.75e-0699738088838
Pubmed

ZBED4, a cone and Müller cell protein in human retina, has a different cellular expression in mouse.

OPN1LW OPN1MW2 OPN1MW3

1.75e-06997321850176
Pubmed

Top2b is involved in the formation of outer segment and synapse during late-stage photoreceptor differentiation by controlling key genes of photoreceptor transcriptional regulatory network.

OPN1LW OPN1MW2 OPN1MW3

1.75e-06997328370415
Pubmed

IFT20 is required for opsin trafficking and photoreceptor outer segment development.

OPN1LW OPN1MW2 OPN1MW3

1.75e-06997321307337
Pubmed

Multilocus molecular mapping of the mouse X chromosome.

OPN1LW OPN1MW2 OPN1MW3

1.75e-0699732906327
Pubmed

A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction.

OPN1LW OPN1MW2 OPN1MW3

1.75e-06997327669145
Pubmed

Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata.

OPN1LW OPN1MW2 OPN1MW3

1.75e-0699731973136
Pubmed

Distinct functions of photoreceptor cell-specific nuclear receptor, thyroid hormone receptor beta2 and CRX in one photoreceptor development.

OPN1LW OPN1MW2 OPN1MW3

1.75e-06997312407160
Pubmed

Retinoid-related orphan nuclear receptor RORbeta is an early-acting factor in rod photoreceptor development.

OPN1LW OPN1MW2 OPN1MW3 PCDH15

1.93e-063297419805139
Pubmed

Mef2d is essential for the maturation and integrity of retinal photoreceptor and bipolar cells.

OPN1LW OPN1MW2 OPN1MW3 PCDH15

1.93e-063297425757744
Pubmed

Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1.

MYO7A PDZD7 PCDH15

2.49e-061097324618850
Pubmed

Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3.

OPN1LW OPN1MW2 OPN1MW3

2.49e-06109731349842
Pubmed

Cyclophilin-related protein RanBP2 acts as chaperone for red/green opsin.

OPN1LW OPN1MW OPN1MW2

2.49e-06109738857542
Pubmed

Linkage of a gene for neural cell adhesion molecule, L1 (CamL1) to the Rsvp region of the mouse X chromosome.

OPN1LW OPN1MW2 OPN1MW3

2.49e-06109731964443
Pubmed

Vax2 regulates retinoic acid distribution and cone opsin expression in the vertebrate eye.

OPN1LW OPN1MW2 OPN1MW3

2.49e-061097321148184
Pubmed

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function.

OPN1LW OPN1MW2 OPN1MW3

2.49e-061097331949211
Pubmed

Comparative mapping on the mouse and human X chromosomes of a human cDNA clone encoding the vasopressin renal-type receptor (AVP2R).

OPN1LW OPN1MW2 OPN1MW3

2.49e-06109738449515
Pubmed

The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification.

OPN1LW OPN1MW2 OPN1MW3

2.49e-061097332236127
Pubmed

Physical mapping of the loci Gabra3, DXPas8, CamL1, and Rsvp in a region of the mouse X chromosome homologous to human Xq28.

OPN1LW OPN1MW2 OPN1MW3

2.49e-06109731684949
Pubmed

Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome.

OPN1LW OPN1MW2 OPN1MW3

2.49e-06109731973380
Pubmed

Physical linkage of the A-raf-1, properdin, synapsin I, and TIMP genes on the human and mouse X chromosomes.

OPN1LW OPN1MW2 OPN1MW3

3.41e-06119731572636
Pubmed

Mannose supplements induce embryonic lethality and blindness in phosphomannose isomerase hypomorphic mice.

OPN1LW OPN1MW2 OPN1MW3

3.41e-061197324421398
Pubmed

Mapping of the glycine receptor alpha 2-subunit gene and the GABAA alpha 3-subunit gene on the mouse X chromosome.

OPN1LW OPN1MW2 OPN1MW3

4.54e-06129731679744
Pubmed

The spatial patterning of mouse cone opsin expression is regulated by bone morphogenetic protein signaling through downstream effector COUP-TF nuclear receptors.

OPN1LW OPN1MW2 OPN1MW3

4.54e-061297319812316
Pubmed

MAP4K4 is involved in the neuronal development of retinal photoreceptors.

OPN1LW OPN1MW2 OPN1MW3

4.54e-061297337290629
Pubmed

Genetic and physical mapping of the biglycan gene on the mouse X chromosome.

OPN1LW OPN1MW2 OPN1MW3

4.54e-06129738093671
Pubmed

The construction of human somatic cell hybrids containing portions of the mouse X chromosome and their use to generate DNA probes via interspersed repetitive sequence polymerase chain reaction.

OPN1LW OPN1MW2 OPN1MW3

4.54e-06129731916827
Pubmed

Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease.

OPN1LW OPN1MW2 OPN1MW3

4.54e-06129732561974
Pubmed

The expression analysis of Sfrs10 and Celf4 during mouse retinal development.

OPN1LW OPN1MW2 OPN1MW3

5.89e-061397323932931
InteractionPIGY interactions

ERG28 TMEM72 FBXO7

3.18e-067923int:PIGY
GeneFamilyOpsin receptors

OPN1LW OPN1MW OPN1MW2 OPN1MW3

6.66e-0811704215
GeneFamilyWD repeat domain containing|F-box and WD repeat domain containing

FBXW10B FBXW10

7.95e-0411702559
GeneFamilySolute carriers

SLC22A25 SLC4A8 SLC13A3 SLC40A1 SLC50A1 SLC5A8 SLC30A9

8.27e-04395707752
GeneFamilyAminoacyl tRNA synthetases, Class I

EPRS1 VARS1

2.42e-0319702131
GeneFamilyV-type ATPases

TCIRG1 ATP6V0A4

3.55e-0323702415
GeneFamilyClaudins

CLDN22 CLDN19

3.55e-0323702488
GeneFamilyZinc fingers DHHC-type|Ankyrin repeat domain containing

ZDHHC16 ZDHHC15

3.86e-032470276
ToppCell3'-Adult-LargeIntestine-Hematopoietic-Plasma_cells-IgG_plasma_cell|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract

CCR10 TCAF2 SFMBT2 FCRL5 SLAMF7 IL5RA

2.20e-06175966c3d3f11602379aaba65842a98835299e54fccd84
ToppCellParenchymal-NucSeq-Stromal-Schwann|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

BEST1 B4GALNT4 GRIK2 LGI4 PIGH

1.03e-051339658819fd897b97812355e1709fcc42754522d5fb27
ToppCellParenchymal-NucSeq-Stromal-Schwann-Schwann_nonmyelinating|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

BEST1 B4GALNT4 GRIK2 LGI4 PIGH

1.03e-05133965b4e68a9a223e5188f1a00c7dc9bb2d675cde1d40
ToppCellLPS-antiTNF-Epithelial_alveolar-Mes-like|LPS-antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

COX15 PEX11A ANKRD55 MDN1 FGF7

1.07e-0513496564979e1a056b7406e1be39c5ebe2f8d731ac3c17
ToppCellfacs-Lung-Endomucin-24m-Lymphocytic|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

ATP8B3 TMEM72 FCRL5 IL5RA HCRTR2

2.30e-0515796514c4c61790eba6a388679e6d5011424d56cf3b5a
ToppCellrenal_medulla_nuclei-CKD+DKD_normotensive-Immune-Lymphocytic_B|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

TCIRG1 FBXO10 FCRL5 SLAMF7 IL5RA

3.09e-051679650130743084dbcb20e10f96715d30961122150cbf
ToppCellfacs-Trachea-nan-18m-Mesenchymal-chondrocyte|Trachea / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

PDZD7 CPE KCNF1 ATP6V0A4 ATP1A4

3.09e-051679657b1fd19946cee67dae68f0f0d98420abcd532482
ToppCellrenal_medulla_nuclei-CKD+DKD_normotensive-Immune-Lymphocytic_B-Plasma_Cell-|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

TCIRG1 FBXO10 FCRL5 SLAMF7 IL5RA

3.09e-051679657bcae3797d3a0811e7f39885afdfd29ec517f11b
ToppCellrenal_medulla_nuclei-CKD+DKD_normotensive-Immune-Lymphocytic_B-Plasma_Cell|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

TCIRG1 FBXO10 FCRL5 SLAMF7 IL5RA

3.09e-05167965c6f0209a1ad797631fdfa3efab6db6b1d3e8e315
ToppCelldroplet-Liver-Npc-18m-Lymphocytic-B_cell|Liver / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation

ANKRD55 FCRL5 VARS1 IL5RA HCRTR2

3.18e-05168965ce9fae8b295c668b0959d5007a8bcd401d80e258
ToppCelldroplet-Liver-Npc-18m-Lymphocytic-B_cell|Liver / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation

ANKRD55 FCRL5 VARS1 IL5RA HCRTR2

3.46e-05171965584a095ddcbf78aa29527f84b46b5ad3e2edbaa9
ToppCellfacs-Marrow-Granulocytes-3m-Myeloid-macrophage|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

B4GALNT4 TCIRG1 SNX21 ANKRD55 ZDHHC15

3.55e-051729657fb31ccbcd0204c3612986a6bc20d57ed6825e9c
ToppCellfacs-Marrow-Granulocytes-3m-Myeloid-CD4+_macrophage|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

B4GALNT4 TCIRG1 SNX21 ANKRD55 ZDHHC15

3.55e-051729652a4614b3d25e8c6b095e6992d8ca35371dcdb5e1
ToppCellmetastatic_Brain-B_lymphocytes-MALT_B_cells|metastatic_Brain / Location, Cell class and cell subclass

CCR10 IGKV1-8 FCRL5 SLAMF7 IL5RA

3.97e-0517696550e207403d48ce1b55a78897adb5519a2430a626
ToppCellfacs-Marrow-B-cells-18m-Hematologic-Unknown_Progenitor|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CCR10 ANKRD55 FGF7 SLAMF7 HCRTR2

3.97e-051769655f9ae5eb45603ed0422a3a993ecdbe2ce05d6e45
ToppCellsystemic_lupus_erythematosus-flare-Lymphocytic_B-plasmablast|systemic_lupus_erythematosus / PBMC cell types (v2) per disease, treatment status, and sex

CCR10 FBXO10 FCRL5 SLAMF7 ESPL1

3.97e-05176965dc4e939a07bad21ab36181f9588df3fa662f9a92
ToppCellfacs-BAT-Fat-3m-Epithelial|BAT / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TLCD1 TMEM54 PEX11A SMIM38 CARD14

4.07e-051779653e42f6236962dd9bb23dc0d09b460ec8347d1056
ToppCellfacs-GAT-Fat-24m-Lymphocytic-B_cell|GAT / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CCR10 ANKRD55 FCRL5 VARS1 IL5RA

4.07e-05177965f4afe10522eed77318954210224496f09d372532
ToppCellfacs-BAT-Fat-3m-Epithelial-epithelial_cell|BAT / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TLCD1 TMEM54 PEX11A SMIM38 CARD14

4.07e-05177965128186bc996784e670194c07c5352e69af5f6d68
ToppCell3'-Adult-SmallIntestine-Hematopoietic-Plasma_cells-IgA_plasma_cell|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract

TCAF2 COX18 SFMBT2 FCRL5 SLAMF7

4.07e-05177965b326376e879afef579b1b7094d756aaff0de270b
ToppCell3'-Adult-SmallIntestine-Hematopoietic-Plasma_cells|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract

TCAF2 COX18 SFMBT2 FCRL5 SLAMF7

4.07e-05177965393882f1bf7658a17e10a771b803339f16fb2e69
ToppCellfacs-BAT-Fat-3m-Epithelial-nan|BAT / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TLCD1 TMEM54 PEX11A SMIM38 CARD14

4.07e-051779657480e522cfae3f5c6c62720083750f8273725ab5
ToppCell3'-GW_trimst-2-LargeIntestine-Mesenchymal-fibroblastic-mLTo|GW_trimst-2 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

GPR137 CPE LRRIQ4 FGF7 ATP1A4

4.41e-05180965f103e161e966c257eac97e1b30a461c4ed9cafc2
ToppCellfacs-Marrow-B-cells-18m-Hematologic-MPP_Fraction_B_+_C|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TLCD1 SLC4A8 PIGH PRKAA1 PWP2

4.41e-051809657368ab31c3273374ef260f0d710d4eea83cbc4a2
ToppCellnormal_Lymph_Node-B_lymphocytes-Plasma_cells|normal_Lymph_Node / Location, Cell class and cell subclass

CCR10 IGKV1-8 FCRL5 SLAMF7 IL5RA

4.53e-05181965949ac3b60e7fb5968da4c4e872965fb4e10f4a35
ToppCellBAL-Control-Myeloid-Macrophage|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

MYO7A SLC40A1 KCNF1 SLAMF7 ATP1A4

4.77e-051839658e9d45c96b44558158e3d59613f64a73d5390c19
ToppCellBAL-Control-Myeloid-Macrophage-transitional_Macro-|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

MYO7A SLC40A1 KCNF1 SLAMF7 ATP1A4

4.77e-051839650408d991ddb639594b45d5cb2432dd29289167b1
ToppCellBAL-Control-Myeloid-Macrophage-transitional_Macro|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

MYO7A SLC40A1 KCNF1 SLAMF7 ATP1A4

4.77e-0518396579f05b8a967124d831b0baef137e30659f5917a7
ToppCellBAL-Control-Myeloid-Macrophage-transitional_Macro-|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)

MYO7A SLC40A1 KCNF1 SLAMF7 ATP1A4

4.90e-0518496592202e1cd0bba1ce4b061ebcb8a2af5bb590542a
ToppCellBAL-Control-Myeloid-Macrophage|Control / Location, Disease Group, Cell group, Cell class (2021.03.09)

MYO7A SLC40A1 KCNF1 SLAMF7 ATP1A4

4.90e-051849657331535d469453a5264dcb0270a97f63d3b55201
ToppCellBAL-Control-Myeloid-Macrophage-transitional_Macro|Control / Location, Disease Group, Cell group, Cell class (2021.03.09)

MYO7A SLC40A1 KCNF1 SLAMF7 ATP1A4

4.90e-05184965337e38a6b2b6770cc992d88b006829f194841b10
ToppCellPCW_13-14-Mesenchymal-Mesenchymal_fibroblastic-mes_Arw_fibro_(16)|PCW_13-14 / Celltypes from embryonic and fetal-stage human lung

SLC4A8 CPE KCNF1 PCDH15 FGF7

5.03e-051859657dcdc009c5681ee05dd18968f7e85c3403fe34af
ToppCellkidney_cells-Renal_AKI_(acute_kidney_injury)-Immune-Lymphocytic_B-Plasma_Cell-|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group

CCR10 IGKV1-8 FCRL5 SLAMF7 IL5RA

5.03e-051859650fff2608f507e019ebb69c27e58fd5be3b049bef
ToppCellkidney_cells-Renal_AKI_(acute_kidney_injury)-Immune-Lymphocytic_B-Plasma_Cell|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group

CCR10 IGKV1-8 FCRL5 SLAMF7 IL5RA

5.03e-0518596579edc1eeb7b5b9123961ac3ecf398ee68d9dddb9
ToppCell10x_3'_v3-bone_marrow_(10x_3'_v3)-lymphocytic-B_lymphocytic-plasma_cell|bone_marrow_(10x_3'_v3) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

CCR10 IGKV1-8 FCRL5 SLAMF7 IL5RA

5.56e-051899655a42be62552d912d0abf68f00d75ac80bbd69f2c
ToppCellnormal_Lymph_Node-B_lymphocytes-Plasma_cells|B_lymphocytes / Location, Cell class and cell subclass

CCR10 IGKV1-8 FCRL5 SLAMF7 IL5RA

5.99e-05192965119832d4aee29ddda2485fc3e5dcdaacf833cc30
ToppCellTracheal-10x5prime-Immune_Lymphocytic-B-B_plasma-B_plasma_IgA|10x5prime / Cell types per location group and 10X technology with lineage, and cell group designations

CCR10 IGKV1-8 FCRL5 SLAMF7 IL5RA

6.45e-05195965df009b18898c10686f75cf72b4ec0eff18f5bb50
ToppCellmLN-B_cell-B_cell_IgG_Plasma|mLN / Region, Cell class and subclass

CCR10 TMEM54 FCRL5 SLAMF7 IL5RA

6.61e-0519696503b79f237e4f7ebab46b277d05377569c6342cf7
ToppCellmLN-(2)_B_cell-(21)_B_cell_IgG_Plasma|mLN / shred on region, Cell_type, and subtype

CCR10 TMEM54 FCRL5 SLAMF7 IL5RA

6.61e-05196965e8b12b046d42a58e6f4d9419ab05a5c55e764f34
ToppCellCOVID-19-COVID-19_Severe-Lymphocyte-B-Plasmablast|COVID-19_Severe / Disease, condition lineage and cell class

CCR10 EPRS1 FCRL5 SLAMF7 VARS1

7.10e-05199965e6422b65e22e5aa8dfaebdae5be76dd78b978604
ToppCellnormal_Lung-B_lymphocytes-Plasma_cells|normal_Lung / Location, Cell class and cell subclass

CCR10 FBXO10 FCRL5 IL5RA

1.05e-041139647ec8c1712977d3b8e861d2743ff7bd1797ab35df
ToppCellStriatum-Macroglia-ASTROCYTE-Gja1|Striatum / BrainAtlas - Mouse McCarroll V32

CLDN22 CPE LGI4 CLDN19

1.28e-04119964d47880ef1cff036192c43646a04fa8598dd7e1f4
ToppCellStriatum-Macroglia-ASTROCYTE|Striatum / BrainAtlas - Mouse McCarroll V32

CLDN22 CPE LGI4 CLDN19

1.28e-041199640583387cc4497cf991fa42a81f2f66d9c6b774eb
ToppCellFrontal_cortex-Endothelial-ENDOTHELIAL_TIP-Dcn_1-Dcn_1_1-Endothelial_Tip.Dcn.Inmt_(Inmt)|Frontal_cortex / BrainAtlas - Mouse McCarroll V32

TCAF2 EXD1 ATP6V0A4 TNXB

1.37e-041219645035e071033cb76a7fc0128716755b14821e8f05
ToppCellFrontal_cortex-Endothelial-ENDOTHELIAL_TIP-Dcn_1-Dcn_1_1-Endothelial_Tip.Dcn.Inmt_(Inmt)-|Frontal_cortex / BrainAtlas - Mouse McCarroll V32

TCAF2 EXD1 ATP6V0A4 TNXB

1.37e-04121964c96115bd33455296378a257583b49442d00b39ca
Diseaseblue cone monochromacy (implicated_via_orthology)

OPN1LW OPN1MW OPN1MW2 OPN1MW3

7.05e-114874DOID:0050679 (implicated_via_orthology)
DiseaseUsher Syndrome, Type II

MYO7A PDZD7 PCDH15

2.47e-075873C1568249
DiseaseCone monochromatism

OPN1LW OPN1MW

8.59e-062872C0339537
DiseaseBLUE CONE MONOCHROMACY

OPN1LW OPN1MW

8.59e-062872303700
DiseaseCone monochromatism

OPN1LW OPN1MW

8.59e-062872cv:C0339537
Diseaseblue cone monochromacy (is_implicated_in)

OPN1LW OPN1MW

8.59e-062872DOID:0050679 (is_implicated_in)
DiseaseBORNHOLM EYE DISEASE

OPN1LW OPN1MW

8.59e-062872C3159311
DiseaseAchromatopsia incomplete, X-linked

OPN1LW OPN1MW

8.59e-062872C2931753
DiseaseRed-green dyschromatopsia

OPN1LW OPN1MW

8.59e-062872cv:C0155016
DiseaseUsher syndrome type 2

MYO7A PDZD7

2.57e-053872C0339534
DiseaseUsher Syndrome

MYO7A PCDH15

5.14e-054872C0271097
DiseaseUsher syndrome, type 1A

MYO7A PCDH15

8.54e-055872C2931205
Diseaseautosomal recessive osteopetrosis 1 (implicated_via_orthology)

TCIRG1 ATP6V0A4

8.54e-055872DOID:0110942 (implicated_via_orthology)
DiseaseUSHER SYNDROME, TYPE IB (disorder)

MYO7A PCDH15

8.54e-055872C1848638
DiseaseUSHER SYNDROME, TYPE IA, FORMERLY

MYO7A PCDH15

8.54e-055872C1848639
DiseaseUSHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY

MYO7A PCDH15

8.54e-055872C1848640
DiseaseUsher syndrome type 1

MYO7A PCDH15

8.54e-055872cv:C1568247
DiseaseUsher Syndrome, Type I

MYO7A PCDH15

1.28e-046872C1568247
DiseaseHereditary retinal dystrophy

MYO7A PCDH15

1.79e-047872C0154860
DiseaseUsher syndrome

MYO7A PCDH15

1.79e-047872cv:C0271097
DiseaseUsher Syndrome, Type III

MYO7A PCDH15

1.79e-047872C1568248
Diseaserenal tubular acidosis (implicated_via_orthology)

TCIRG1 ATP6V0A4

2.38e-048872DOID:14219 (implicated_via_orthology)
Diseasecongenital disorder of glycosylation type I (implicated_via_orthology)

DOLK RFT1

8.80e-0415872DOID:0050570 (implicated_via_orthology)
DiseaseX-11470 measurement

TNXB VARS1

1.42e-0319872EFO_0021241
DiseaseHuntington's disease (is_implicated_in)

GRIK2 PRKAA1

2.09e-0323872DOID:12858 (is_implicated_in)
Diseasegout

LHFPL3 SLC13A3 BDKRB2 ATP1A4

2.73e-03196874EFO_0004274
Diseasedocosapentaenoic acid measurement

BEST1 TNXB

2.88e-0327872EFO_0006809

Protein segments in the cluster

PeptideGeneStartEntry
LYSLVIWGCTLLLSS

BDKRB2

176

P30411
WSLGSATCRTISGLY

CCR10

106

P46092
RTKGRTWYILSLTLC

C6orf136

186

Q5SQH8
SSIVLYWLCSSFVGL

COX18

276

Q8N8Q8
VAVLLLWLSCYGSAL

CATSPERE

6

Q5SY80
AVVYTCSLDGIVRLW

AAMP

371

Q13685
SIRYWDLKSGVCTRI

FBXW10

476

Q5XX13
CSLVCRAWYELILSL

FBXO10

26

Q9UK96
FILAGLCTLTAVSWY

CLDN19

126

Q8N6F1
SFSRLLLCWRGSIYK

BEST1

16

O76090
ATYLGWLEGCVSLLR

ANKRD55

101

Q3KP44
IKYWTALCVATILLS

ATP8B3

1136

O60423
IVWATSYLIGCAIAS

CRISP1

146

P54107
YTVSLCGITGLWSLA

OPN1LW

131

P04000
YTVSLCGITGLWSLA

OPN1MW3

131

P0DN78
LVLSYLLTRWCGSVG

RFT1

416

Q96AA3
LVVVLYAWGVACSLT

OR5D16

146

Q8NGK9
YTVSLCGITGLWSLA

OPN1MW2

131

P0DN77
SIRYWDLKSGVCTRI

FBXW10B

476

O95170
LLIWGFDILCITNSY

OR52N4

206

Q8NGI2
TLVRWYTANCLALVT

MDN1

181

Q9NU22
LAYWSLLATLACLVV

DOLK

301

Q9UPQ8
ICRWTSLHLLYLGNT

LRRIQ4

276

A6NIV6
LSYQTVFLALCLLWA

GPR137

56

Q96N19
LTCTALITYACWGQL

FUT4

161

P22083
LVATILSCGWIIYLT

KIAA1109

31

Q2LD37
RWLSDCLSHQYGILL

EXD1

161

Q8NHP7
QWVRIACLALGTTEY

DUOX2

1301

Q9NRD8
TWSVISLLRGEAYVC

CALHM2

116

Q9HA72
GLAAGALLLYCWLSR

FCRL5

861

Q96RD9
VSEYCWLDRLSNGVL

PDZD7

301

Q9H5P4
LVIINSCLWDLSRYG

PCED1A

136

Q9H1Q7
RTFGIWTLLSSVIRC

ERG28

51

Q9UKR5
SWADGLALCALVYRL

MICAL1

536

Q8TDZ2
SDLWALGCIIYQLVA

PDPK2P

236

Q6A1A2
YGCSSLVSRILQEAW

EIF2B4

336

Q9UI10
YTVSLCGITGLWSLA

OPN1MW

131

P04001
SVLTLSCIALDRWYA

HCRTR2

141

O43614
YLWTCLASGIILGSL

PCDH15

6

Q96QU1
LSLLGWVLSCLTNYL

CLDN22

16

Q8N7P3
LSLTCDLLRSQLYWT

ESPL1

856

Q14674
LRSYQVSLHCTWLVG

IL5RA

146

Q01344
WTALIRSTLACILEY

HEATR5B

1831

Q9P2D3
WAESCLTLVPYTLVR

CARD14

806

Q9BXL6
CWLVSYSLAVLLLGC

B3GNT4

31

Q9C0J1
FCLTVLYSLIGRKLW

GHSR

226

Q92847
LRSHLRQSLLCTWGY

FBXO7

26

Q9Y3I1
LAASISWILYCLALN

CYP4X1

321

Q8N118
AWRIYVTLLSTLNSC

FFAR3

256

O14843
VWLQCTAISRIYTVG

CPE

66

P16870
ITCRASQGISSYLAW

IGKV1-8

41

A0A0C4DH67
LVLYCASLWTSLSLL

COX15

231

Q7KZN9
WLYTLCASLSRLVVK

FHOD1

206

Q9Y613
LCLLWIGYSQGTTHV

GRIK2

21

Q13002
LTWILPTLLYRSCFH

FGF7

6

P21781
LRWSYLQLAIVGTCA

SLC22A25

176

Q6T423
YWCTEALPLSVTALL

SLC13A3

51

Q8WWT9
SLCWVLSVLYGLIHT

OR1D2

146

P34982
YTCLLSSTWQELILL

NR6A1

316

Q15406
ISHRPCLLSYSLLFW

SND1-IT1

46

Q9HBX3
GIIYRSTRLVNWSCT

VARS1

466

P26640
YLVGNSLSLADLCVW

EPRS1

111

P07814
ARCWYILLSGSVLVK

RAPGEF6

71

Q8TEU7
RTERSVSCLWGGLLY

TCAF2

601

A6NFQ2
FAGRCLILSWDYSLQ

LGI4

241

Q8N135
YISQCWTLGSVLALT

PTDSS2

411

Q9BVG9
ILLARLILWSCLGTY

SMIM38

21

A0A286YFK9
LILWSCLGTYIDYRL

SMIM38

26

A0A286YFK9
YINLVGLWAILTCSV

SLC5A8

281

Q8N695
GWVLTSCYILIITIA

SLC40A1

126

Q9NP59
YFICDTILWVRSVGL

PEX11A

96

O75192
ALSYLSLRACIGLWT

SLC4A8

556

Q2Y0W8
RWILASCTDLYGELL

MED13

1801

Q9UHV7
VDIWSSGVILYALLC

PRKAA1

206

Q13131
LLSCAAWLTYVHLGL

B4GALNT4

21

Q76KP1
LLWTGAILCFVAYSI

ATP1A4

111

Q13733
WSSYNLIILGLAGCR

TAS2R5

41

Q9NYW4
SSYSLPLLLCKVFRW

SMAD7

151

O15105
RIYSSSLCLWGIALV

TMEM54

151

Q969K7
LFITWNGEISSLYLC

STKLD1

91

Q8NE28
CWAATTTEGLLIYSL

PWP2

716

Q15269
TCTGLYREALALWAN

SNX21

251

Q969T3
IATLLTSASWCLYGF

SLC50A1

166

Q9BRV3
NSLLISCAVSYRGAW

TNXB

4176

P22105
YWVATIITTCGQLLL

SFMBT2

91

Q5VUG0
LTAVTCTVWLAAYGL

PIGH

41

Q14442
TCLTLIYILWQLTGS

SLAMF7

6

Q9NQ25
IETAWSLSGYLLVCF

TLCD1

76

Q96CP7
SLVYLWFLCSSVALA

ZDHHC16

266

Q969W1
CLGCISNTASYLRLW

ATP6V0A4

731

Q9HBG4
YGRLRGTLSALLSWC

YAE1

76

Q9NRH1
SLLWAYCILAGSLVS

SLC30A9

341

Q6PML9
FWTGLEYTCRLLGIT

TMEM72

6

A0PK05
LLIRSYGLCWTISIT

PTDSS1

181

P48651
GCVSNTASYLRLWAL

TCIRG1

726

Q13488
SLVILFGYHCWLVSR

ZDHHC15

226

Q96MV8
ETACIGWFTLEYLLR

KCNF1

226

Q9H3M0
LGACSVRWAYILAII

LHFPL3

181

Q86UP9
SSYARGWILVSLCVG

MYO7A

1186

Q13402