ENSMUSG00000055553


Mus musculus

Features
Gene ID: ENSMUSG00000055553
  
Biological name :Kxd1
  
Synonyms : Kxd1 / KxDL motif-containing protein 1 / Q80XH1
  
Possible biological names infered from orthology : KxDL motif containing 1 / Q9BQD3
  
Species: Mus musculus
  
Chr. number: 8
Strand: -1
Band: B3.3
Gene start: 70508272
Gene end: 70527956
  
Corresponding Affymetrix probe sets: 10454805 (MoGene1.0st)   10511342 (MoGene1.0st)   10579302 (MoGene1.0st)   10579307 (MoGene1.0st)   10591208 (MoGene1.0st)   10594904 (MoGene1.0st)   10603009 (MoGene1.0st)   1416624_a_at (Mouse Genome 430 2.0 Array)   1428180_at (Mouse Genome 430 2.0 Array)   1430258_at (Mouse Genome 430 2.0 Array)   1452701_x_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000113804
Ensembl peptide - ENSMUSP00000123679
Ensembl peptide - ENSMUSP00000123548
Ensembl peptide - ENSMUSP00000123438
Ensembl peptide - ENSMUSP00000121539
Ensembl peptide - ENSMUSP00000113816
Ensembl peptide - ENSMUSP00000091165
Ensembl peptide - ENSMUSP00000112561
NCBI entrez gene - 75620     See in Manteia.
MGI - MGI:1922870
RefSeq - NM_029366
RefSeq Peptide - NP_083642
swissprot - D3YXX6
swissprot - D3YWA5
swissprot - G3X9Z9
swissprot - E9QNP0
swissprot - Q80XH1
swissprot - E9Q4P0
swissprot - D3Z2M8
Ensembl - ENSMUSG00000055553
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 kxd1ENSDARG00000051934Danio rerio
 KXD1ENSGALG00000036736Gallus gallus
 KXD1ENSG00000105700Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR000626  Ubiquitin domain
 IPR001975  Ribosomal protein L40e
 IPR011332  Zinc-binding ribosomal protein
 IPR019371  Uncharacterised domain KxDL
 IPR019954  Ubiquitin conserved site
 IPR019956  Ubiquitin
 IPR029071  Ubiquitin-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006412 translation IEA
 biological_processGO:0016192 vesicle-mediated transport IMP
 biological_processGO:0032418 lysosome localization IEA
 cellular_componentGO:0005764 lysosome IEA
 cellular_componentGO:0005765 lysosomal membrane IEA
 cellular_componentGO:0005840 ribosome IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0031083 BLOC-1 complex IDA
 cellular_componentGO:0099078 BORC complex IEA
 molecular_functionGO:0003735 structural constituent of ribosome IEA
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0010192 abnormal retinal melanin granule morphology "any structural anomaly of the pigment particles in the retina" [ISBN-13:978-1-4051-2034-0 "The Pigmentary System, Second Edition"]
Show

Allelic Composition: Hspa5baffled/Hspa5baffled
Genetic Background: FVB.Cg-Hspa5baffled

 MP:0010193 abnormal choroid melanin granule morphology "any structural anomaly of the pigment particles in the choroid" [ISBN-13:978-1-4051-2034-0 "The Pigmentary System, Second Edition"]
Show

Allelic Composition: Hspa5baffled/Hspa5baffled
Genetic Background: FVB.Cg-Hspa5baffled

 MP:0020432 decreased platelet dense granule number "decreased number of the electron-dense bodies occurring in blood platelets that store and secrete adenosine nucleotides and serotonin" [orcid.org/0000-0003-4606-0597]
Show

Allelic Composition: Hspa5baffled/Hspa5baffled
Genetic Background: FVB.Cg-Hspa5baffled

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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