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Center for Computational Systems Medicine
Soverview

Gene summary

Soverview

Spatial pattern genes

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Spatial pattern pathway

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Cell cell interactions using single cell data

Soverview

Cell-cell/spot-spot interactions using spatial data

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Transcription factors events

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Related drugs with this gene

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Related diseases with this gene

Spatial pattern gene: Ccdc50 (spascer ID:67501)

Gene summary for Ccdc50

check button Gene summary
Gene information
SpeciesMouse
Gene symbol

Ccdc50

Gene ID

67501

Gene namecoiled-coil domain containing 50
SynonymsC3orf6
Cytomap16 B2|16 18.98 cM
Type of geneprotein-coding
Descriptioncoiled-coil domain-containing protein 50protein Ymer
Modification date20220424
UniProtAcc

Q810U5


check button Gene ontology with evidence Inferred from Direct Assay (IDA) and Biological aspect of Ancestor (IBA).
GeneGO IDGO termPubMed IDCategory
Ccdc50

GO:0005737

cytoplasm

21873635

Component
Ccdc50

GO:0031625

ubiquitin protein ligase binding

21873635

Function

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Spatial pattern events for Ccdc50

check buttonspatial pattern gene list.
Gene symbolSpeciesTissueReplicationPMIDAdj p-value
Ccdc50MouseEmbryorep_4 331887763.23e-08
Ccdc50MouseBrainrep_1 334690252.41e-13
Ccdc50MouseBrainrep_1 350277291.84e-06
Ccdc50MouseBrainrep_2 350277293.83e-08
Ccdc50MouseBrainrep_3 350277293.13e-14
Ccdc50MouseBrainrep_4 350277291.16e-10
Ccdc50MouseTesticlerep_1 347316001.63e-03
Ccdc50MouseLymphPBS 05.63e-08
Ccdc50MouseBrainrep_1 352106241.74e-15
Ccdc50MouseBrainrep_2 352106241.74e-15
Ccdc50MouseBrainrep_3 352106246.25e-15
Ccdc50MouseBrainrep_5 352106241.04e-13
Ccdc50MouseBrainrep_6 352106242.05e-15
Ccdc50MouseBrainrep_7 352106241.87e-15

check buttonspatial pattern gene map.(click to enlarge the image in a new window)

H&E staining (if available)Singel gene map
Brain_rep_1_H&E
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Brain_rep_1_H&E
boxplot

boxplot
Brain_rep_2_H&E
boxplot

boxplot
Brain_rep_3_H&E
boxplot

boxplot
Brain_rep_4_H&E
boxplot

boxplot


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Spatial pattern pathway has Ccdc50 envolved


SymbolPathwaySpeciesTissue typeReplicationP-value
Ccdc50GOBP_Nervous_System_ProcessMouseSpinal cordL7bCN02_E1 2.5e-06
Ccdc50GOBP_Sensory_PerceptionMouseSpinal cordL7CN45_C1 5.0e-07
Ccdc50GOBP_Sensory_Perception_Of_Mechanical_StimulusMouseSpinal cordL7CN45_C1 2.4e-07
Ccdc50GOBP_Nervous_System_ProcessMouseBrainrep_1 1.6e-36
Ccdc50GOBP_Sensory_PerceptionMouseBrainrep_3 2.9e-57
Ccdc50GOBP_Sensory_Perception_Of_Mechanical_StimulusMouseBrainrep_31.7e-132
Ccdc50GOBP_Sensory_PerceptionMouseEmbryorep_14 5.0e-07
Ccdc50GOBP_Sensory_Perception_Of_Mechanical_StimulusMouseEmbryorep_14 1.6e-53
Ccdc50GOBP_Nervous_System_ProcessMouseEmbryorep_1 1.4e-08
Ccdc50GOBP_Sensory_PerceptionMouseEmbryorep_3 0.0e+00
Ccdc50GOBP_Sensory_Perception_Of_Mechanical_StimulusMouseEmbryorep_38.3e-301
Ccdc50GOBP_Nervous_System_ProcessMouseKidneyrep_2 1.9e-90
Ccdc50GOBP_Sensory_PerceptionMouseKidneyrep_2 1.4e-94
Ccdc50GOBP_Sensory_Perception_Of_Mechanical_StimulusMouseKidneyrep_2 3.0e-69
Ccdc50GOBP_Nervous_System_ProcessMouseLiverCN73-C1 1.7e-08
Ccdc50GOBP_Nervous_System_ProcessMouseLymphMS-1 1.4e-08
Ccdc50GOBP_Sensory_PerceptionMouseLymphMS-1 5.2e-11
Ccdc50GOBP_Sensory_Perception_Of_Mechanical_StimulusMouseLymphMS-1 9.0e-11
Ccdc50GOBP_Nervous_System_ProcessMouseBrainHP_ad_rep7 7.0e-10
Ccdc50GOBP_Sensory_PerceptionMouseBrainHP_polb_rep9 1.2e-09

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Ccdc50 function as liang/receptor in single cell data

TissueSourceSourceCellTargetTargetCellPMIDGroup

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Ccdc50 function as liang/receptor across spatial transcriptomics tissue

check button Interactions using deconvoluted spatial data.

LigandReceptor LR pairTissueReplication

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Transcription factor for Ccdc50 envolved

check buttonTranscription factor analysis using single cell data.
TFTissueGroupCell typesTarget genesRss score

check button Motif information.

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Related Drugs for Ccdc50

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.9 2022-01-04)
GeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for Ccdc50

check button Diseases associated with this gene.
(DisGeNet 7.0)
GeneDisease IDDisease namePubmedsSource
Ccdc50C3711374Nonsyndromic Deafness3CLINGEN
Ccdc50C1384666hearing impairment1GENOMICS_ENGLAND
Ccdc50C1843895Deafness, Autosomal Dominant 441CTD_human;GENOMICS_ENGLAND