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- DFNB31 abstract "Whirlin is a protein that in humans is encoded by the DFNB31 gene.In rat brain, WHRN interacts with a calmodulin-dependent serine kinase, CASK, and may be involved in the formation of scaffolding protein complexes that facilitate synaptic transmission in the central nervous system (CNS). Mutations in this gene, also known as WHRN, cause autosomal recessive deafness.".
- DFNB31 entrezgene "25861".
- DFNB31 wikiPageExternalLink br.fcgi?book=gene&part=usher2.
- DFNB31 wikiPageID "14812635".
- DFNB31 wikiPageLength "11672".
- DFNB31 wikiPageOutDegree "25".
- DFNB31 wikiPageRevisionID "695531091".
- DFNB31 wikiPageWikiLink Auditory_brainstem_response.
- DFNB31 wikiPageWikiLink CASK.
- DFNB31 wikiPageWikiLink Category:Genes_mutated_in_mice.
- DFNB31 wikiPageWikiLink Clinical_chemistry.
- DFNB31 wikiPageWikiLink Dual-energy_X-ray_absorptiometry.
- DFNB31 wikiPageWikiLink Gene.
- DFNB31 wikiPageWikiLink Glucose_tolerance_test.
- DFNB31 wikiPageWikiLink Hearing_loss.
- DFNB31 wikiPageWikiLink Hematology.
- DFNB31 wikiPageWikiLink Hot_plate_test.
- DFNB31 wikiPageWikiLink Indirect_calorimetry.
- DFNB31 wikiPageWikiLink International_Knockout_Mouse_Consortium.
- DFNB31 wikiPageWikiLink Knockout_mouse.
- DFNB31 wikiPageWikiLink Micronucleus_test.
- DFNB31 wikiPageWikiLink Model_organism.
- DFNB31 wikiPageWikiLink Mutant.
- DFNB31 wikiPageWikiLink Open_Field_(animal_test).
- DFNB31 wikiPageWikiLink Peripheral_blood_lymphocyte.
- DFNB31 wikiPageWikiLink Phenotypic_screening.
- DFNB31 wikiPageWikiLink Protein.
- DFNB31 wikiPageWikiLink Radiography.
- DFNB31 wikiPageWikiLink Teratology.
- DFNB31 wikiPageWikiLink Zygosity.
- DFNB31 wikiPageWikiLinkText "DFNB31".
- DFNB31 wikiPageWikiLinkText "WHRN".
- DFNB31 requireManualInspection "no".
- DFNB31 summaryText "In rat brain, WHRN interacts with a calmodulin-dependent serine kinase, CASK, and may be involved in the formation of scaffolding protein complexes that facilitate synaptic transmission in the central nervous system . Mutations in this gene, also known as WHRN, cause autosomal recessive deafness.".
- DFNB31 updateCitations "yes".
- DFNB31 updatePage "yes".
- DFNB31 updateProteinBox "yes".
- DFNB31 updateSummary "yes".
- DFNB31 wikiPageUsesTemplate Template:Cite_journal.
- DFNB31 wikiPageUsesTemplate Template:PBB.
- DFNB31 wikiPageUsesTemplate Template:PBB_Controls.
- DFNB31 wikiPageUsesTemplate Template:PBB_Further_reading.
- DFNB31 wikiPageUsesTemplate Template:PBB_Summary.
- DFNB31 wikiPageUsesTemplate Template:PDB_Gallery.
- DFNB31 wikiPageUsesTemplate Template:Refbegin.
- DFNB31 wikiPageUsesTemplate Template:Refend.
- DFNB31 wikiPageUsesTemplate Template:Reflist.
- DFNB31 subject Category:Genes_mutated_in_mice.
- DFNB31 hypernym Protein.
- DFNB31 type Biomolecule.
- DFNB31 type Protein.
- DFNB31 type Page.
- DFNB31 type Thing.
- DFNB31 type Q206229.
- DFNB31 type Q8054.
- DFNB31 comment "Whirlin is a protein that in humans is encoded by the DFNB31 gene.In rat brain, WHRN interacts with a calmodulin-dependent serine kinase, CASK, and may be involved in the formation of scaffolding protein complexes that facilitate synaptic transmission in the central nervous system (CNS). Mutations in this gene, also known as WHRN, cause autosomal recessive deafness.".
- DFNB31 label "DFNB31".
- DFNB31 sameAs Q18037755.
- DFNB31 sameAs Whirlina.
- DFNB31 sameAs m.03gys8r.
- DFNB31 sameAs Q18037755.
- DFNB31 wasDerivedFrom DFNB31?oldid=695531091.
- DFNB31 isPrimaryTopicOf DFNB31.