ENSMUSG00000028718


Mus musculus

Features
Gene ID: ENSMUSG00000028718
  
Biological name :Stil
  
Synonyms : SCL-interrupting locus protein homolog isoform 5 / Stil
  
Possible biological names infered from orthology : Q15468 / STIL, centriolar assembly protein
  
Species: Mus musculus
  
Chr. number: 4
Strand: 1
Band: D1
Gene start: 115000159
Gene end: 115043196
  
Corresponding Affymetrix probe sets: 10507112 (MoGene1.0st)   1427707_a_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000120836
Ensembl peptide - ENSMUSP00000123385
Ensembl peptide - ENSMUSP00000030490
Ensembl peptide - ENSMUSP00000118849
NCBI entrez gene - 20460     See in Manteia.
MGI - MGI:107477
RefSeq - XM_017320088
RefSeq - NM_001304551
RefSeq - NM_001304553
RefSeq - NM_001304555
RefSeq - NM_001304559
RefSeq - NM_009185
RefSeq - XM_006502905
RefSeq - XM_006502907
RefSeq Peptide - NP_001291482
RefSeq Peptide - NP_001291484
RefSeq Peptide - NP_001291488
RefSeq Peptide - NP_033211
RefSeq Peptide - NP_001291480
swissprot - A2AD39
swissprot - D6RH61
swissprot - F6VXM5
swissprot - A0A1B0GXH2
Ensembl - ENSMUSG00000028718
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 stilENSDARG00000024904Danio rerio
 STILENSGALG00000010478Gallus gallus
 STILENSG00000123473Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR026123  SCL-interrupting locus protein


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007052 mitotic spindle organization IEA
 biological_processGO:0046599 regulation of centriole replication IEA
 biological_processGO:0051298 centrosome duplication IEA
 biological_processGO:0071539 protein localization to centrosome IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005813 centrosome IEA
 cellular_componentGO:0005814 centriole IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000926 absent floor plate "missing ventral midline thinning of the developing neural tube" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:35802]
Show

Allelic Composition: Sim1tm1Fan/Sim1+,Sim2tm1Fan/Sim2+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0001648 abnormal apoptosis "excessive or absent cell death in a particular tissue or cell type" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:25248]
Show

Allelic Composition: Sim1tm1Fan/Sim1+,Sim2tm1Fan/Sim2+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Ptch1tm1Zim/Ptch1tm1Zim,Stiltm1Mku/Stiltm1Mku
Genetic Background: involves: 129/Sv

 MP:0001706 abnormal left-right axis patterning "anomaly in the formation or development of the body or a specific organ of the body in relation to the left and right sides of the body or organ" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Sim1tm1Fan/Sim1+,Sim2tm1Fan/Sim2+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0002151 abnormal neural tube morphology/development "anomalous structure of or development of the embryonic neural tube resulting in structural anomaly" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Sim1tm1Fan/Sim1+,Sim2tm1Fan/Sim2+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0002621 delayed neural tube closure "delayed fusion of the neuroepithelial layer in early development" [J:79790, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
Show

Allelic Composition: Sim1tm1Fan/Sim1+,Sim2tm1Fan/Sim2+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0003984 embryonic growth retardation "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Sim1tm1Fan/Sim1+,Sim2tm1Fan/Sim2+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0004712 notochord degeneration "retrogressive pathologic change of the axial fibrocellular cord in embryos around which develops the vertebral primordia (prior to normal differentiation of this tissue into the vertebral column tissues)" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Sim1tm1Fan/Sim1+,Sim2tm1Fan/Sim2+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0005157 holoprosencephaly "presence of a single forebrain hemisphere or lobe; often accompanied by a deficit in median facial development" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83058]
Show

Allelic Composition: Sim1tm1Fan/Sim1+,Sim2tm1Fan/Sim2+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Ptch1tm1Zim/Ptch1tm1Zim,Stiltm1Mku/Stiltm1Mku
Genetic Background: involves: 129/Sv

 MP:0011098 complete embryonic lethality during organogenesis "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
Show

Allelic Composition: Sim1tm1Fan/Sim1+,Sim2tm1Fan/Sim2+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Ptch1tm1Zim/Ptch1tm1Zim,Stiltm1Mku/Stiltm1Mku
Genetic Background: involves: 129/Sv

  


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






 

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