Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionG protein-coupled receptor activity

OPN1MW2 OR14K1 OPN1MW3 OR51B5 GPR15 GPR20 OR51B6 OR5B17 ADGRG1 OPN1MW GPR132

3.87e-068844611GO:0004930
GeneOntologyMolecularFunctionG protein-coupled photoreceptor activity

OPN1MW2 OPN1MW3 OPN1MW

5.11e-0615463GO:0008020
GeneOntologyMolecularFunctionphotoreceptor activity

OPN1MW2 OPN1MW3 OPN1MW

7.61e-0617463GO:0009881
GeneOntologyMolecularFunctionantiporter activity

SLC32A1 SLC35E2A SLC44A2 SLC7A5 SLC35E2B

1.60e-05138465GO:0015297
GeneOntologyMolecularFunctiontransmembrane signaling receptor activity

OPN1MW2 OR14K1 OPN1MW3 OR51B5 GPR15 GPR20 OR51B6 OR5B17 ADGRG1 OPN1MW GPR132 IL4R

4.00e-0513534612GO:0004888
GeneOntologyMolecularFunctionsecondary active transmembrane transporter activity

SLC6A1 SLC32A1 SLC35E2A SLC44A2 SLC7A5 SLC35E2B

5.74e-05296466GO:0015291
GeneOntologyMolecularFunctiongamma-aminobutyric acid transmembrane transporter activity

SLC6A1 SLC32A1

1.85e-049462GO:0015185
GeneOntologyMolecularFunctiontransporter activity

SLC6A1 SLC32A1 GJB3 TRPC4AP CLCNKA SLC35E2A SLC44A2 SLC7A5 ATP10B SLC35E2B

5.83e-0412894610GO:0005215
GeneOntologyMolecularFunctionactive transmembrane transporter activity

SLC6A1 SLC32A1 SLC35E2A SLC44A2 SLC7A5 SLC35E2B

7.50e-04477466GO:0022804
GeneOntologyMolecularFunctionsecondary active monocarboxylate transmembrane transporter activity

SLC6A1 SLC32A1

8.66e-0419462GO:0015355
GeneOntologyMolecularFunctionorganic cation transmembrane transporter activity

SLC32A1 SLC44A2 SLC7A5

9.24e-0483463GO:0015101
GeneOntologyMolecularFunctiontransmembrane transporter activity

SLC6A1 SLC32A1 GJB3 TRPC4AP CLCNKA SLC35E2A SLC44A2 SLC7A5 SLC35E2B

1.29e-031180469GO:0022857
GeneOntologyMolecularFunctionamino acid transmembrane transporter activity

SLC6A1 SLC32A1 SLC7A5

1.82e-03105463GO:0015171
GeneOntologyMolecularFunctionamino acid:monoatomic cation symporter activity

SLC6A1 SLC32A1

2.03e-0329462GO:0005416
GeneOntologyMolecularFunctionneutral L-amino acid transmembrane transporter activity

SLC32A1 SLC7A5

4.02e-0341462GO:0015175
GeneOntologyCellularComponentphotoreceptor disc membrane

OPN1MW2 OPN1MW3 OPN1MW

2.85e-0526483GO:0097381
DomainOpsin_red/grn

OPN1MW3 OPN1MW

1.86e-053472IPR000378
Domain7tm_1

OR14K1 OPN1MW3 OR51B5 GPR15 GPR20 OR51B6 OR5B17 OPN1MW GPR132

4.06e-05677479PF00001
DomainG_PROTEIN_RECEP_F1_1

OR14K1 OPN1MW3 OR51B5 GPR15 GPR20 OR51B6 OR5B17 OPN1MW GPR132

4.45e-05685479PS00237
DomainG_PROTEIN_RECEP_F1_2

OR14K1 OPN1MW3 OR51B5 GPR15 GPR20 OR51B6 OR5B17 OPN1MW GPR132

4.76e-05691479PS50262
DomainGPCR_Rhodpsn

OR14K1 OPN1MW3 OR51B5 GPR15 GPR20 OR51B6 OR5B17 OPN1MW GPR132

4.81e-05692479IPR000276
DomainGPCR_Rhodpsn_7TM

OPN1MW3 OR51B5 GPR15 GPR20 OR51B6 OR5B17 OPN1MW GPR132

2.40e-04670478IPR017452
DomainSugar_P_trans_dom

SLC35E2A SLC35E2B

2.75e-0410472IPR004853
DomainOPSIN

OPN1MW3 OPN1MW

2.75e-0410472PS00238
DomainTPT

SLC35E2A SLC35E2B

2.75e-0410472PF03151
DomainOpsin

OPN1MW3 OPN1MW

3.36e-0411472IPR001760
DomainZF_BBOX

TRIM43B MYCBP2 TRIM43

1.07e-0380473PS50119
DomainZnf_B-box

TRIM43B MYCBP2 TRIM43

1.11e-0381473IPR000315
DomainARM-type_fold

STK36 TRPC4AP ATM RALGAPA2

1.03e-02339474IPR016024
PathwayREACTOME_THE_RETINOID_CYCLE_IN_CONES_DAYLIGHT_VISION

OPN1MW2 OPN1MW3

1.76e-048362MM14880
PathwayREACTOME_TRANSPORT_OF_SMALL_MOLECULES

SLC6A1 SLC32A1 TRPC4AP CLCNKA SLC44A2 SLC7A5 ATP10B SOAT2

2.58e-04681368MM14985
PathwayREACTOME_OPSINS

OPN1MW2 OPN1MW3

2.82e-0410362MM15063
PathwayREACTOME_TRANSPORT_OF_SMALL_MOLECULES

SLC6A1 SLC32A1 TRPC4AP CLCNKA SLC44A2 SLC7A5 ATP10B SOAT2

4.37e-04736368M27287
PathwayREACTOME_INTERLEUKIN_4_AND_INTERLEUKIN_13_SIGNALING

SOCS5 IL4R

5.66e-0414362MM15321
Pubmed

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

OPN1MW2 OPN1MW3 OPN1MW

1.05e-08449329386880
Pubmed

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

OPN1MW2 OPN1MW3 OPN1MW

2.62e-0854932937147
Pubmed

Hydrogen/Deuterium Exchange Mass Spectrometry of Human Green Opsin Reveals a Conserved Pro-Pro Motif in Extracellular Loop 2 of Monostable Visual G Protein-Coupled Receptors.

OPN1MW2 OPN1MW

1.94e-06249228402104
Pubmed

SLC35E2 promoter mutation as a prognostic marker of esophageal squamous cell carcinoma.

SLC35E2A SLC35E2B

1.94e-06249235247439
Pubmed

Defective colour vision associated with a missense mutation in the human green visual pigment gene.

OPN1MW2 OPN1MW

1.94e-0624921302020
Pubmed

Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype.

OPN1MW2 OPN1MW

1.94e-06249210319869
Pubmed

Molecular determinants of human red/green color discrimination.

OPN1MW2 OPN1MW

5.83e-0634928185948
Pubmed

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

OPN1MW2 OPN1MW

5.83e-06349220579627
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349238410159
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349223350963
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349220471354
Pubmed

Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.

OR51B5 OR51B6

5.83e-06349220018918
Pubmed

Multiple hypothalamic cell populations encoding distinct visual information.

OPN1MW2 OPN1MW3

5.83e-06349221224225
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349228751656
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349236216501
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349231469404
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349211545071
Pubmed

Mechanisms of spectral tuning in the mouse green cone pigment.

OPN1MW2 OPN1MW3

5.83e-0634929238068
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349217379811
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349210567724
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349234111401
Pubmed

Plasmalemmal and vesicular gamma-aminobutyric acid transporter expression in the developing mouse retina.

SLC6A1 SLC32A1

5.83e-06349218975268
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349212511072
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-0634927958444
Pubmed

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

OPN1MW2 OPN1MW3

5.83e-06349214500905
Pubmed

Chromatin Remodeling Enzyme Snf2h Is Essential for Retinal Cell Proliferation and Photoreceptor Maintenance.

OPN1MW2 OPN1MW3 ATM

1.04e-053049337048108
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449226438865
Pubmed

Characteristic development of the GABA-removal system in the mouse spinal cord.

SLC6A1 SLC32A1

1.16e-05449224412234
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449217249565
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449238060327
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449234126082
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449216567464
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449231461375
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449224801621
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-0544928088841
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449228103478
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449228528909
Pubmed

Molecular biology of the visual pigments.

OPN1MW2 OPN1MW

1.16e-0544923303660
Pubmed

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

OPN1MW2 OPN1MW3

1.16e-05449231846668
Pubmed

Melanopsin-driven light adaptation in mouse vision.

OPN1MW2 OPN1MW3

1.16e-05449225308073
Pubmed

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

OPN1MW2 OPN1MW3

1.94e-05549236631163
Pubmed

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

OPN1MW2 OPN1MW3

1.94e-05549226818794
Pubmed

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

OPN1MW2 OPN1MW3

1.94e-0554921333116
Pubmed

Melanopsin-based brightness discrimination in mice and humans.

OPN1MW2 OPN1MW3

1.94e-05549222633808
Pubmed

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

OPN1MW2 OPN1MW3

1.94e-05549211055434
Pubmed

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

OPN1MW2 OPN1MW3

1.94e-05549222090509
Pubmed

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

OPN1MW2 OPN1MW3

1.94e-05549210723722
Pubmed

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

OPN1MW2 OPN1MW3

1.94e-05549224058409
Pubmed

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

OPN1MW2 OPN1MW3

1.94e-05549234099749
Pubmed

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

OPN1MW2 OPN1MW3

1.94e-05549227033727
Pubmed

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

OPN1MW2 OPN1MW3

2.91e-05649223288843
Pubmed

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

OPN1MW2 OPN1MW3

2.91e-0564928872469
Pubmed

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

OPN1MW2 OPN1MW3

2.91e-05649211138006
Pubmed

GRK1-dependent phosphorylation of S and M opsins and their binding to cone arrestin during cone phototransduction in the mouse retina.

OPN1MW2 OPN1MW

2.91e-05649212853434
Pubmed

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

OPN1MW2 OPN1MW3

2.91e-05649210395695
Pubmed

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

OPN1MW2 OPN1MW3

2.91e-05649217436273
Pubmed

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

OPN1MW2 OPN1MW3

2.91e-0564921549575
Pubmed

Expression of the suppressor of cytokine signaling-5 (SOCS5) negatively regulates IL-4-dependent STAT6 activation and Th2 differentiation.

SOCS5 IL4R

2.91e-05649212242343
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.

OPN1MW2 OPN1MW3

4.07e-0574928378320
Pubmed

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

OPN1MW2 OPN1MW3

4.07e-05749218974269
Pubmed

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

OPN1MW2 OPN1MW3

4.07e-05749230799247
Pubmed

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

OPN1MW2 OPN1MW3

4.07e-05749216574740
Pubmed

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

OPN1MW2 OPN1MW3

4.07e-05749229180667
Pubmed

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

OPN1MW2 OPN1MW3

4.07e-0574928001979
Pubmed

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

OPN1MW2 OPN1MW3

4.07e-05749218199774
Pubmed

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

OPN1MW2 OPN1MW3

4.07e-0574929880679
Pubmed

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

OPN1MW2 OPN1MW3

4.07e-05749219332056
Pubmed

X-chromosome gene order in different Mus species crosses.

OPN1MW2 OPN1MW3

5.42e-0584923416629
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-05849212651948
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-05849231163126
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-05849220203194
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-05849223351594
Pubmed

Localization of the mdx mutation within the mouse dystrophin gene.

OPN1MW2 OPN1MW3

5.42e-0584922903046
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-05849210725384
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-05849216043864
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-05849233007388
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-0584921572654
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-0584921675194
Pubmed

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

OPN1MW2 OPN1MW3

5.42e-05849221813673
Pubmed

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

OPN1MW2 OPN1MW3

6.96e-05949214742273
Pubmed

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

OPN1MW2 OPN1MW3

6.96e-05949227669145
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.

OPN1MW2 OPN1MW3

6.96e-0594921973136
Pubmed

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

OPN1MW2 OPN1MW3

6.96e-05949225296752
Pubmed

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

OPN1MW2 OPN1MW3

6.96e-0594928088838
Pubmed

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

OPN1MW2 OPN1MW3

6.96e-05949212407160
Pubmed

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

OPN1MW2 OPN1MW3

6.96e-05949221850176
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.

OPN1MW2 OPN1MW3

6.96e-05949228370415
Pubmed

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

OPN1MW2 OPN1MW3

6.96e-05949221307337
Pubmed

Multilocus molecular mapping of the mouse X chromosome.

OPN1MW2 OPN1MW3

6.96e-0594922906327
Pubmed

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

OPN1MW2 OPN1MW3

8.69e-051049221148184
Pubmed

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

OPN1MW2 OPN1MW3

8.69e-051049231949211
Pubmed

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

OPN1MW2 OPN1MW3

8.69e-05104928449515
Pubmed

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

OPN1MW2 OPN1MW3

8.69e-05104921349842
Pubmed

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

OPN1MW2 OPN1MW3

8.69e-051049232236127
Pubmed

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

OPN1MW2 OPN1MW3

8.69e-05104921684949
Pubmed

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

OPN1MW2 OPN1MW3

8.69e-05104921973380
Pubmed

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

OPN1MW2 OPN1MW

8.69e-05104928857542
Pubmed

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

OPN1MW2 OPN1MW3

8.69e-05104921964443
Pubmed

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

OPN1MW2 OPN1MW3

1.06e-041149224421398
Pubmed

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

OPN1MW2 OPN1MW3

1.06e-04114921572636
Cytoband2q11.1

TRIM43B TRIM43

4.14e-04284922q11.1
Cytoband3q25.1

MED12L TMEM14EP

5.77e-04334923q25.1
CytobandEnsembl 112 genes in cytogenetic band chr3q11

GPR15 CLDND1

1.54e-0354492chr3q11
CytobandEnsembl 112 genes in cytogenetic band chrXq28

OPN1MW2 OPN1MW3 OPN1MW

1.55e-03213493chrXq28
Cytoband1p36.33

SLC35E2A SLC35E2B

3.10e-03774921p36.33
GeneFamilyOpsin receptors

OPN1MW2 OPN1MW3 OPN1MW

1.40e-0611383215
GeneFamilySolute carriers

SLC6A1 SLC32A1 SLC35E2A SLC44A2 SLC7A5 SLC35E2B

1.60e-04395386752
GeneFamilyG protein-coupled receptors, Class A orphans

GPR15 GPR20 GPR132

5.84e-0478383262
GeneFamilyOlfactory receptors, family 51

OR51B5 OR51B6

3.85e-0344382164
ToppCellHippocampus-Neuronal-Excitatory-eN1(Slc17a7)-eN1_2-Nxph3-Excitatory_Neuron.Slc17a7.Nxph3-Ajap1_(Entorhinal_cortex)|Hippocampus / BrainAtlas - Mouse McCarroll V32

TRIM43 OPN1MW SOAT2

2.03e-05494830b3e9c8f166be5d6aab318da4b87176427637877
ToppCellprimary_visual_cortex-Neuronal-GABAergic_neuron-Sst-Sst_Myh8_Fibin|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype

SLC6A1 SLC32A1 ADGRG1 IL4R

2.46e-05157484741d79c10cb87fa7f14080c6fccb1553c3a20bad
ToppCellCOPD-Myeloid-pDC|World / Disease state, Lineage and Cell class

SLC32A1 BRF1 MED12L SLC7A5

3.68e-05174484be8227398300711ccda5ecc41ad34064bb246b19
ToppCellMid-temporal_gyrus_(MTG)-Neuronal-Glutamatergic_Excit-Glut_A_(CT)-Glut_CT_L6_FEZF2-Exc_L6_FEZF2_CPZ|Mid-temporal_gyrus_(MTG) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

TRIM43B OR51B5 OR51B6 TRIM43

4.20e-05180484a499548391e6833b78f6e920f8e32a755814a9da
ToppCellfacs-Brain_Myeloid-Striatum-3m-Myeloid-nan|Brain_Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TRPC4AP TM9SF3 SLC44A2 MED12L

5.08e-051894846dd4ec5ce4beb856f0d2d1654e3c4676d1d63736
ToppCellfacs-Brain_Myeloid-Striatum-3m-Myeloid|Brain_Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TRPC4AP TM9SF3 SLC44A2 MED12L

5.08e-051894843ae479ec7e00c57127cbe51a398329b10ca9848c
ToppCellfacs-Brain_Myeloid-Striatum-3m-Myeloid-microglial_cell|Brain_Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TRPC4AP TM9SF3 SLC44A2 MED12L

5.08e-05189484875df61ee48baa5142ba4d2427bdec1c53e5a828
ToppCellfacs-Brain_Myeloid-Striatum-3m|Brain_Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TRPC4AP TM9SF3 SLC44A2 MED12L

5.08e-0518948497ef5215d841ff366a3e3682cd9bd04100cbfde0
ToppCell3'-Pediatric_IBD-SmallIntestine-Epithelial-goblet|Pediatric_IBD / Celltypes from developing, pediatric, Crohn's, & adult GI tract

ABHD2 TM9SF3 ATP10B GPA33

5.73e-05195484c5f33b420c9ac14dc67fea632b8c2bc2442cbf3d
ToppCellkidney_cells-Adult_normal_reference-Epithelial-Distal_tubule_epithelial_cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

CLCNKA ADGRG1 SLC7A5 SHISA3

5.73e-051954843123e02d2894c83962ba402085b5e6422ebf8c73
ToppCell3'-Pediatric_IBD-SmallIntestine-Epithelial-goblet-Goblet_cell|Pediatric_IBD / Celltypes from developing, pediatric, Crohn's, & adult GI tract

ABHD2 TM9SF3 ATP10B GPA33

5.73e-05195484219c5d0cde7f6082755154f54db221413ec555cb
ToppCellkidney_cells-Hypertensive_with+without-CKD-Epithelial-Distal_tubule_epithelial_cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

CLCNKA ADGRG1 SLC7A5 SHISA3

6.08e-05198484688b0eb5534dde40b8630ab8a3252c816711e02e
ToppCellSmart-start-Cell-Wel_seq-Non-neoplastic-Glial-Neuronal-OPC-OPC-G|Smart-start-Cell-Wel_seq / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group

SLC6A1 ABHD2 ATP10B CDH18

6.20e-0519948419a97e27a4758e794ce7246d295e112b47931a48
ToppCellFetal_brain-fetalBrain_Zhong_nature-GW23|fetalBrain_Zhong_nature / Sample Type, Dataset, Time_group, and Cell type.

SLC6A1 SLC32A1 SPAAR SLC35E2B

6.20e-05199484f30e9d3d095a1e12d759debe27540aad32861db6
Diseaseblue cone monochromacy (implicated_via_orthology)

OPN1MW2 OPN1MW3 OPN1MW

1.32e-084453DOID:0050679 (implicated_via_orthology)
Diseasefetal hemoglobin measurement

OR51B5 OR51B6

4.69e-0421452EFO_0004576
Diseaselung squamous cell carcinoma (is_implicated_in)

SLC7A5 ATM

6.14e-0424452DOID:3907 (is_implicated_in)
Diseasepulse pressure measurement, diastolic blood pressure, systolic blood pressure, hypertension

GPR20 CDH18

1.31e-0335452EFO_0000537, EFO_0005763, EFO_0006335, EFO_0006336
DiseaseAnorectal Malformations

RFX6 CDH18

1.80e-0341452C3495676

Protein segments in the cluster

PeptideGeneStartEntry
VSVIYCSGTDRLCAC

BIRC6

941

Q9NR09
KVLCCVSVCQGYSAL

ABHD2

226

P08910
VPLLSIVTCYCCIAR

GPR15

206

P49685
CSILFLTCICVDRYL

GPR20

136

Q99678
LELTQYCRSVLCCRS

ATP10B

1016

O94823
TCCITPLSIIVLCYL

OPN1MW3

226

P0DN78
NYIVCEGVCLPRCIL

RFX6

131

Q8HWS3
TCCITPLSIIVLCYL

OPN1MW2

226

P0DN77
LCISYLKSETCGCRI

MKKS

126

Q9NPJ1
TTGLCVCIVAVLRRY

MED12L

876

Q86YW9
VAALIIIGIIIYCCC

GPA33

246

Q99795
CIVCKRSYVCLTSLR

ZBTB33

496

Q86T24
GVCYAFSCLVCIVVS

OR14K1

201

Q8NGZ2
LITCVSHICCVLVFY

OR51B5

236

Q9H339
SHICCILVFYVTVVC

OR51B6

241

Q9H340
CLCVLLLTAVNCYSV

SLC7A5

176

Q01650
LCTSVIFLGCCIVIL

MANSC4

291

A6NHS7
YARCIAVCSLGVWIC

RALGAPA2

1156

Q2PPJ7
TCCITPLSIIVLCYL

OPN1MW

226

P04001
VRCSRLLVGVLGCYC

ATM

716

Q13315
CIVILAVCLLCYVSI

IL4R

241

P24394
LACLVTIAAYLCSRV

ADGRG1

416

Q9Y653
PVLVCLCFVQRCYGT

CDH18

11

Q13634
YCRQASCVSLLCRPV

KRTAP10-9

261

P60411
IYNRGCTDIICCVFL

SLC44A2

26

Q8IWA5
AVCIVLTICELCYLI

GJB3

196

O75712
TRVCACLAIGCYVIG

OR5B17

136

Q8NGF7
IYVSILFLCCISCDR

GPR132

126

Q9UNW8
VLFVVTVAITCVLCC

SPAAR

26

A0A1B0GVQ0
VICLNYLVDPVTICC

TRIM43

16

Q96BQ3
LLCCVLTSVGATCCY

TMEM41A

106

Q96HV5
VYRDSIIVCCINSCT

SLC6A1

316

P30531
ICVLVGVFICSICVK

SEMA3C

6

Q99985
CLSILYNTCVCTEGV

TRPC4AP

166

Q8TEL6
PFSLQYICRAVICRC

SOCS5

481

O75159
ILGSVVAIYCCTCLR

SHISA3

111

A0PJX4
TVIGCVKTLVPCCLY

SLC35E2A

116

P0CK97
FVGTCCLRLLRVYTC

MYCBP2

1461

O75592
KVLYSCCLVSEGLCR

STK36

716

Q9NRP7
GCVLYACFILGRLCV

SOAT2

306

O75908
LIGLCACICRSLYPT

CLDND1

156

Q9NY35
ICGVLSCAYLFCQRT

CLCNKA

291

P51800
CEFVGTLVCRCQYIL

STAG3L4

51

Q8TBR4
TVIGCVKTLVPCCLY

SLC35E2B

116

P0CK96
VIAACLYLVCRTEGT

BRF1

131

Q92994
LCIVTVCVTIVCTYF

TM9SF3

491

Q9HD45
VICLNYLVDPVTICC

TRIM43B

16

A6NCK2
AVVCCYTGKILIACL

SLC32A1

156

Q9H598
NIYACGFSCRCLLIV

TMEM14EP

86

Q6UXP3