Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionG protein-coupled photoreceptor activity

OPN1MW2 OPN1MW3 OPN1MW

4.78e-0615453GO:0008020
GeneOntologyMolecularFunctionphotoreceptor activity

OPN1MW2 OPN1MW3 OPN1MW

7.11e-0617453GO:0009881
GeneOntologyBiologicalProcessdetection of visible light

OPN1MW2 OPN1MW3 IRX6 OPN1MW

7.18e-0657454GO:0009584
GeneOntologyBiologicalProcessdetection of light stimulus

OPN1MW2 OPN1MW3 IRX6 OPN1MW

2.38e-0577454GO:0009583
GeneOntologyCellularComponentphotoreceptor disc membrane

OPN1MW2 OPN1MW3 OPN1MW

2.34e-0526453GO:0097381
HumanPhenoAbnormal left hemidiaphragm morphology

WT1 GATA6

5.99e-055132HP:0040046
HumanPhenoAplasia of the left hemidiaphragm

WT1 GATA6

5.99e-055132HP:0040048
HumanPhenoAplasia of the left hemidiaphragm

WT1 GATA6

5.99e-055132HP:0009112
HumanPhenoAbnormal hemidiaphragm morphology

WT1 GATA6

1.25e-047132HP:0040045
HumanPhenoDenervation of the diaphragm

WT1 GATA6

1.25e-047132HP:0009109
HumanPhenoBicuspid aortic valve

WT1 GATA6 NOTCH3 SCAF4

1.72e-04119134HP:0001647
HumanPhenoAbnormal aortic valve cusp morphology

WT1 GATA6 NOTCH3 SCAF4

1.83e-04121134HP:0031567
HumanPhenoAplasia/Hypoplasia of the diaphragm

WT1 GATA6

2.14e-049132HP:0010315
DomainOpsin_red/grn

OPN1MW3 OPN1MW

1.48e-053422IPR000378
DomainOPSIN

OPN1MW3 OPN1MW

2.20e-0410422PS00238
DomainOpsin

OPN1MW3 OPN1MW

2.68e-0411422IPR001760
DomainIntegrin_alpha

ITGAD ITGAX

2.68e-0411422PF00357
DomainIntegrin_alpha_C_CS

ITGAD ITGAX

5.81e-0416422IPR018184
DomainIntegrin_alpha-2

ITGAD ITGAX

7.38e-0418422IPR013649
DomainIntegrin_alpha2

ITGAD ITGAX

7.38e-0418422PF08441
DomainIntegrin_alpha

ITGAD ITGAX

7.38e-0418422IPR000413
DomainINTEGRIN_ALPHA

ITGAD ITGAX

7.38e-0418422PS00242
DomainInt_alpha_beta-p

ITGAD ITGAX

8.24e-0419422IPR013519
DomainInt_alpha

ITGAD ITGAX

8.24e-0419422SM00191
DomainFG_GAP

ITGAD ITGAX

1.11e-0322422PS51470
DomainFG-GAP

ITGAD ITGAX

1.32e-0324422PF01839
DomainFG-GAP

ITGAD ITGAX

1.32e-0324422IPR013517
DomainIntegrin_dom

ITGAD ITGAX

1.43e-0325422IPR032695
DomainHomeodomain-like

HOXA13 IRX6 KDM1B NKX2-4

6.45e-03332424IPR009057
DomainVWA

ITGAD ITGAX

7.04e-0356422PF00092
DomainHomeobox_CS

HOXA13 IRX6 NKX2-4

8.39e-03186423IPR017970
DomainRRM_1

CPEB2 RBFOX2 SCAF4

1.14e-02208423PF00076
DomainRRM

CPEB2 RBFOX2 SCAF4

1.27e-02217423SM00360
PathwayREACTOME_THE_RETINOID_CYCLE_IN_CONES_DAYLIGHT_VISION

OPN1MW2 OPN1MW3

1.14e-048292MM14880
PathwayREACTOME_OPSINS

OPN1MW2 OPN1MW3

1.82e-0410292MM15063
Pubmed

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

OPN1MW2 OPN1MW3 OPN1MW

8.09e-09445329386880
Pubmed

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

OPN1MW2 OPN1MW3 OPN1MW

2.02e-0854532937147
Pubmed

Onecut1 and Onecut2 redundantly regulate early retinal cell fates during development.

OPN1MW2 OPN1MW3 IRX6 BSN

2.91e-074345425228773
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

1.64e-06245228402104
Pubmed

Mapping of the human CD11c (ITGAX) and CD11d (ITGAD) genes demonstrates that they are arranged in tandem separated by no more than 11.5 kb.

ITGAD ITGAX

1.64e-0624529598326
Pubmed

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

OPN1MW2 OPN1MW

1.64e-0624521302020
Pubmed

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

OPN1MW2 OPN1MW

1.64e-06245210319869
Pubmed

Molecular determinants of human red/green color discrimination.

OPN1MW2 OPN1MW

4.91e-0634528185948
Pubmed

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

OPN1MW2 OPN1MW

4.91e-06345220579627
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345238410159
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345223350963
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345220471354
Pubmed

Multiple hypothalamic cell populations encoding distinct visual information.

OPN1MW2 OPN1MW3

4.91e-06345221224225
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345228751656
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345236216501
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345231469404
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345211545071
Pubmed

Mechanisms of spectral tuning in the mouse green cone pigment.

OPN1MW2 OPN1MW3

4.91e-0634529238068
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345217379811
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345210567724
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345234111401
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345212511072
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-0634527958444
Pubmed

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

OPN1MW2 OPN1MW3

4.91e-06345214500905
Pubmed

Rbpj cell autonomous regulation of retinal ganglion cell and cone photoreceptor fates in the mouse retina.

OPN1MW2 OPN1MW3 NOTCH3

5.15e-062645319828801
Pubmed

Nuclear receptor TLX prevents retinal dystrophy and recruits the corepressor atrophin1.

OPN1MW2 OPN1MW3 ATN1

8.87e-063145316702404
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445226438865
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445217249565
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445238060327
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445234126082
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445216567464
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445231461375
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445224801621
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-0644528088841
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445228103478
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445228528909
Pubmed

Molecular biology of the visual pigments.

OPN1MW2 OPN1MW

9.81e-0644523303660
Pubmed

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

OPN1MW2 OPN1MW3

9.81e-06445231846668
Pubmed

Melanopsin-driven light adaptation in mouse vision.

OPN1MW2 OPN1MW3

9.81e-06445225308073
Pubmed

A Stromal Niche Defined by Expression of the Transcription Factor WT1 Mediates Programming and Homeostasis of Cavity-Resident Macrophages.

WT1 GATA6

1.63e-05545231231034
Pubmed

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

OPN1MW2 OPN1MW3

1.63e-05545236631163
Pubmed

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

OPN1MW2 OPN1MW3

1.63e-05545226818794
Pubmed

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

OPN1MW2 OPN1MW3

1.63e-0554521333116
Pubmed

Melanopsin-based brightness discrimination in mice and humans.

OPN1MW2 OPN1MW3

1.63e-05545222633808
Pubmed

Deficiency of CD11b or CD11d results in reduced staphylococcal enterotoxin-induced T cell response and T cell phenotypic changes.

ITGAD ITGAX

1.63e-05545215210787
Pubmed

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

OPN1MW2 OPN1MW3

1.63e-05545211055434
Pubmed

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

OPN1MW2 OPN1MW3

1.63e-05545222090509
Pubmed

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

OPN1MW2 OPN1MW3

1.63e-05545210723722
Pubmed

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

OPN1MW2 OPN1MW3

1.63e-05545224058409
Pubmed

CD11a regulates hematopoietic stem and progenitor cells.

ITGAD ITGAX

1.63e-05545237781399
Pubmed

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

OPN1MW2 OPN1MW3

1.63e-05545234099749
Pubmed

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

OPN1MW2 OPN1MW3

1.63e-05545227033727
Pubmed

CD11c regulates hematopoietic stem and progenitor cells under stress.

ITGAD ITGAX

1.63e-05545233351105
Pubmed

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

OPN1MW2 OPN1MW3

2.45e-05645223288843
Pubmed

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

OPN1MW2 OPN1MW3

2.45e-0564528872469
Pubmed

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

OPN1MW2 OPN1MW3

2.45e-05645211138006
Pubmed

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

OPN1MW2 OPN1MW

2.45e-05645212853434
Pubmed

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

OPN1MW2 OPN1MW3

2.45e-05645210395695
Pubmed

Unique functions of Gata4 in mouse liver induction and heart development.

WT1 GATA6

2.45e-05645226687508
Pubmed

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

OPN1MW2 OPN1MW3

2.45e-05645217436273
Pubmed

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

OPN1MW2 OPN1MW3

2.45e-0564521549575
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

3.42e-0574528378320
Pubmed

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

OPN1MW2 OPN1MW3

3.42e-05745218974269
Pubmed

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

OPN1MW2 OPN1MW3

3.42e-05745230799247
Pubmed

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

OPN1MW2 OPN1MW3

3.42e-05745216574740
Pubmed

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

OPN1MW2 OPN1MW3

3.42e-05745229180667
Pubmed

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

OPN1MW2 OPN1MW3

3.42e-0574528001979
Pubmed

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

OPN1MW2 OPN1MW3

3.42e-05745218199774
Pubmed

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

OPN1MW2 OPN1MW3

3.42e-0574529880679
Pubmed

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

OPN1MW2 OPN1MW3

3.42e-05745219332056
Pubmed

X-chromosome gene order in different Mus species crosses.

OPN1MW2 OPN1MW3

4.56e-0584523416629
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-05845212651948
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-05845231163126
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-05845220203194
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-05845223351594
Pubmed

Localization of the mdx mutation within the mouse dystrophin gene.

OPN1MW2 OPN1MW3

4.56e-0584522903046
Pubmed

Epicardial GATA factors regulate early coronary vascular plexus formation.

WT1 GATA6

4.56e-05845224380800
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-05845210725384
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-05845216043864
Pubmed

Hepatocyte nuclear factor 4 alpha is related to survival of the condensed mesenchyme in the developing mouse kidney.

WT1 GATA6

4.56e-05845220235219
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-05845233007388
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-0584521572654
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-0584521675194
Pubmed

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

OPN1MW2 OPN1MW3

4.56e-05845221813673
Pubmed

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

OPN1MW2 OPN1MW3

5.86e-05945214742273
Pubmed

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

OPN1MW2 OPN1MW3

5.86e-05945227669145
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

5.86e-0594521973136
Pubmed

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

OPN1MW2 OPN1MW3

5.86e-05945225296752
Pubmed

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

OPN1MW2 OPN1MW3

5.86e-0594528088838
Pubmed

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

OPN1MW2 OPN1MW3

5.86e-05945212407160
Pubmed

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

OPN1MW2 OPN1MW3

5.86e-05945221850176
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

5.86e-05945228370415
Pubmed

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

OPN1MW2 OPN1MW3

5.86e-05945221307337
Pubmed

Multilocus molecular mapping of the mouse X chromosome.

OPN1MW2 OPN1MW3

5.86e-0594522906327
Pubmed

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

OPN1MW2 OPN1MW3

7.32e-051045221148184
Pubmed

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

OPN1MW2 OPN1MW3

7.32e-051045231949211
Pubmed

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

OPN1MW2 OPN1MW3

7.32e-05104528449515
Pubmed

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

OPN1MW2 OPN1MW3

7.32e-05104521349842
Pubmed

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

OPN1MW2 OPN1MW3

7.32e-051045232236127
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

7.32e-05104521684949
InteractionRERE interactions

ATN1 RBFOX2 PRRC2B ALG13

4.57e-0593434int:RERE
InteractionDMRTB1 interactions

CPEB2 RBFOX2 PRRC2B ALG13

4.76e-0594434int:DMRTB1
CytobandEnsembl 112 genes in cytogenetic band chrXq28

OPN1MW2 OPN1MW3 OPN1MW

1.21e-03213453chrXq28
GeneFamilyOpsin receptors

OPN1MW2 OPN1MW3 OPN1MW

4.86e-0711273215
GeneFamilyCD molecules|Integrin alpha subunits

ITGAD ITGAX

3.24e-04182721160
GeneFamilyRNA binding motif containing

CPEB2 RBFOX2 SCAF4

3.83e-03213273725
CoexpressionGSE17721_CTRL_VS_CPG_8H_BMDC_DN

GPR137B HOXA13 MAPKAPK2 DDHD1 NOTCH3

1.66e-05200425M3768
ToppCellrenal_medulla_nuclei-Renal_AKI_(acute_kidney_injury)-Epithelial-Intermediate_tubule_epithelial_cell-kidney_loop_of_Henle_thin_ascending_limb_epithelial_cell-Ascending_Thin_Limb_Cell|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group

DLGAP3 DLEC1 BSN KCTD11

8.26e-061304441720f16ac06951c3f57b6c3b0944670a571203d1
ToppCellSmart-seq2-lymph_node_(Smart-seq2)-lymphocytic-T_lymphocytic-type_I_NK_T_cell|lymph_node_(Smart-seq2) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

KIDINS220 KDM1B ITGAX MN1

1.31e-05146444447c05414eda71681a0c07baba900f88ed6165ed
ToppCellLeuk-UTI-Lymphocyte-T_NK-gdT|Leuk-UTI / Disease, Lineage and Cell Type

TBC1D19 GATA6 ITGAD RBFOX2

1.78e-05158444c4b0af25608cee3d0d2b0193f5ff45d9dc87078b
ToppCellPND07-28-samps-Myeloid-Macrophage-macrophage-B|PND07-28-samps / Age Group, Lineage, Cell class and subclass

CDK2AP2 ITGAX RAB44 DDHD1

1.87e-05160444694bf1f1952bd8ab444819f533da24fa2b73f701
ToppCelldroplet-Marrow-BM-30m-Lymphocytic-plasma_cell|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

GPR137B ITGAD ITGAX PYGO1

2.06e-05164444758e85e2f5e7236b345e16c78344d5e0bf17d8dc
ToppCellfacs-Lung-Endomucin-3m-Mesenchymal-pericyte_cell|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

LSM14B MN1 NOTCH3 RBFOX2

2.32e-051694442d23b4cee060f8adddc430c1c10d4e25205b4af6
ToppCellfacs-Lung-Endomucin-3m-Mesenchymal-Pericyte|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

LSM14B MN1 NOTCH3 RBFOX2

2.32e-05169444ecaf08e8e0b54d1c97a02bc1f65409fd43d68227
ToppCellfacs-Lung-Endomucin-3m-Mesenchymal|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

LSM14B MN1 NOTCH3 RBFOX2

2.32e-05169444ad6af6609acf158cb79e45ee7ca9af332be3c40c
ToppCelldroplet-Lung-nan-3m-Myeloid-Proliferating_Alveolar_Macrophage|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

OPN1MW ITGAX RAB44 DDHD1

2.84e-05178444de6cd81e6d58e7687386df163471bf1901b9c0aa
ToppCelldroplet-Lung-immune-endo-depleted-3m-Myeloid-Alveolar_Macrophage|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

GPR137B ITGAX RAB44 DDHD1

3.30e-05185444775b72319ef6acffd2c9a74293b9c1bccea33f42
ToppCellLV-14._Fibroblast_III|World / Chamber and Cluster_Paper

WT1 TMEM184C MN1 ALG13

3.59e-051894443922135d1f6fc768d71ba3b465585fead6ea68a8
ToppCelldroplet-Fat-Gat-18m-Mesenchymal-Cd34+|Fat / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

WT1 GATA6 ENPP2 SULT1E1

3.74e-051914446cab0334f76c973880bd8d1638856f2f6e4a249a
ToppCelldroplet-Fat-Gat-18m-Mesenchymal|Fat / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

WT1 GATA6 ENPP2 SULT1E1

3.74e-05191444850c6fff6dc795431ef534fdaa41e4ad50f7367a
ToppCellfacs-GAT|facs / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

WT1 GATA6 ENPP2 SULT1E1

3.74e-051914441f5d1e8c313a8dc83c06d2ee45f369b0ec507fbf
ToppCelldroplet-Fat-Gat-18m-Mesenchymal-mesenchymal_stem_cell_of_adipose|Fat / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

WT1 GATA6 ENPP2 SULT1E1

3.74e-051914448b2b00202d3c98bccbae1b4a23713892fad0ff23
ToppCellLV-14._Fibroblast_III|LV / Chamber and Cluster_Paper

WT1 TMEM184C MN1 ALG13

3.98e-05194444927c26aea0147f7a4b8fb3f192de4de263f1b978
ToppCellBrain_organoid-organoid_Tanaka_cellReport-2m-Neuronal-Intermediate|2m / Sample Type, Dataset, Time_group, and Cell type.

KIDINS220 RBFOX2 PRRC2B CCSER2

4.48e-052004442a635694844ddabcd98462c5636a6f41a3f08a46
ToppCellFrontal_cortex-Macroglia-OLIGODENDROCYTE-O2-Tnr-Oligodendrocyte.Tnf.Igsf8_(Ctps)-|Frontal_cortex / BrainAtlas - Mouse McCarroll V32

ITGAD NKX2-4 RAB44

6.55e-0579443eddad041c0bc6952d9c68a36bdd78f6d661f0e58
ToppCellFrontal_cortex-Macroglia-OLIGODENDROCYTE-O2-Tnr-Oligodendrocyte.Tnf.Igsf8_(Ctps)|Frontal_cortex / BrainAtlas - Mouse McCarroll V32

ITGAD NKX2-4 RAB44

6.55e-05794434c9c3051cb8a9c39c6df20e3fe37242db4b44280
Diseaseblue cone monochromacy (implicated_via_orthology)

OPN1MW2 OPN1MW3 OPN1MW

1.15e-084433DOID:0050679 (implicated_via_orthology)
DiseaseFeeding difficulties

ATN1 MN1

3.13e-0418432C0232466
Diseaseupper face morphology measurement

GPR137B DLEC1 ENPP2

3.86e-0497433EFO_0010949
DiseaseCongenital diaphragmatic hernia

WT1 GATA6

4.28e-0421432C0235833
Diseasecongenital heart disease (is_implicated_in)

GATA6 RBFOX2

5.61e-0424432DOID:1682 (is_implicated_in)
DiseaseThyroid Gland Follicular Adenoma

ENPP2 PRDM2

1.20e-0335432C0151468
Diseasesex interaction measurement, Crohn's disease

BSN MAPKAPK2

1.34e-0337432EFO_0000384, EFO_0008343
DiseaseThyroid Neoplasm

ENPP2 PRDM2

1.34e-0337432C0040136
DiseaseDiaphragmatic Hernia

WT1 GATA6

1.64e-0341432C0019284
DiseaseThyroid carcinoma

ENPP2 PRDM2

1.89e-0344432C0549473
DiseaseAcute Promyelocytic Leukemia

WT1 ITGAX

2.06e-0346432C0023487

Protein segments in the cluster

PeptideGeneStartEntry
PPSPMGHYQGFGHTV

TMEM184C

391

Q9NVA4
NRHNMPGPKVDFYPG

ALG13

666

Q9NP73
RPHVMSPGNRNHPFY

ATN1

891

P54259
GSMYAPAQFQPGFIP

CECR2

741

Q9BXF3
QSGFLPHGVPSSGYM

CECR2

846

Q9BXF3
AAANPGYPFHPLMAA

OPN1MW3

291

P0DN78
MAGGGPQANPDYLFH

RAB44

821

Q7Z6P3
MQNEPLTPGYHGFPA

RBFOX2

1

O43251
SGGAFLYPPNMSPTF

ITGAX

376

P20702
MSFPHFGHPYRGASQ

IRX6

1

P78412
AAANPGYPFHPLMAA

OPN1MW2

291

P0DN77
FGPPMFVYTRPHPNS

OR4F21

251

O95013
SGMTGPQHPFYNRPF

KIDINS220

1126

Q9ULH0
ATYHMPPGVSQFPHG

NKX2-4

91

Q9H2Z4
PPGVSQFPHGAMGSY

NKX2-4

96

Q9H2Z4
PPFYSNHGLAISPGM

MAPKAPK2

261

P49137
SPFQPHVPYSPFRGM

LSM14B

106

Q9BX40
HAQRPEPMDGSGPYF

FER1L4

501

A9Z1Z3
AFRPTGHYAGQTPMP

BSN

3111

Q9UPA5
GQAMVFPYHRPSPGS

NOTCH3

1551

Q9UM47
AAANPGYPFHPLMAA

OPN1MW

291

P04001
GGAFLYPPNMSPTFI

ITGAD

376

Q13349
PLGHFESYGGMPFFQ

CCSER2

631

Q9H7U1
ARFPYSPSPPMANGA

GATA6

261

Q92908
PLFNDFGPPSMGYVQ

CDK2AP2

46

O75956
HVPGMNRYFQPFYQP

KDM1B

261

Q8NB78
GFYPGLPSSMNPAFF

CPEB2

11

Q7Z5Q1
SSTFPRMYPGQGPFD

DLGAP3

86

O95886
GLPMGTYQAFPNIHP

IST1

256

P53990
MNYPGRGSPRSPEHN

DDHD1

1

Q8NEL9
FFPHFSQGMLGPYQQ

DLEC1

1186

Q9Y238
GFPGDGMQQPAYTQH

SCAF4

321

O95104
HKYGPFGPEMTNPLR

ENPP2

316

Q13822
PPFQYHHRNPMGIGV

PRDM2

1301

Q13029
GGPMLPSQHAQFEYP

MN1

396

Q10571
FGPPMFVYTRPHPNS

OR4F3;

251

Q6IEY1
YVFNPNPGLFAVMHP

CFAP221

656

Q4G0U5
PMPPNLNSQGGGHYF

KCTD11

11

Q693B1
GMVPSHGFSPRSYFF

GPR137B

326

O60478
PGFGGYSTFRMPPHV

PYGO1

96

Q9Y3Y4
FPQNPLGMGFNRPHA

PYGO1

131

Q9Y3Y4
RFYEMFGHPQPGSAN

SHLD1

101

Q8IYI0
PSYFAHFHSGGMPAP

PRR32

276

B1ATL7
SGYYPCARMGPHPNA

HOXA13

176

P31271
FFLMVAGHPNPGSFP

SULT1E1

141

P49888
SSGQARMFPNAPYLP

WT1

121

P19544
PQRTFYPHHPQMLGF

PRRC2B

656

Q5JSZ5
NLAAPHGPGAFFRYM

ZIC4

106

Q8N9L1
NGVIPFHGFSMYVAP

TBC1D19

361

Q8N5T2