ENSMUSG00000030123


Mus musculus

Features
Gene ID: ENSMUSG00000030123
  
Biological name :Plxnd1
  
Synonyms : plexin D1 / Plxnd1 / Q3UH93
  
Possible biological names infered from orthology : Q9Y4D7
  
Species: Mus musculus
  
Chr. number: 6
Strand: -1
Band: E3
Gene start: 115954811
Gene end: 115995005
  
Corresponding Affymetrix probe sets: 10547100 (MoGene1.0st)   1451475_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000015511
Ensembl peptide - ENSMUSP00000115650
NCBI entrez gene - 67784     See in Manteia.
MGI - MGI:2154244
RefSeq - NM_026376
RefSeq Peptide - NP_080652
swissprot - F6T0L5
swissprot - Q3UH93
Ensembl - ENSMUSG00000030123
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 plxnd1ENSDARG00000086057Danio rerio
 PLXND1ENSGALG00000008473Gallus gallus
 PLXND1ENSG00000004399Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Plxnb1 / Q8CJH3 / plexin B1 / O43157*ENSMUSG0000005364634
Plxnb3 / Q9QY40 / Plexin-B3 / Q9ULL4*ENSMUSG0000003138533
B2RXS4 / Plxnb2 / plexin B2 / O15031*ENSMUSG0000003660631
P70206 / Plxna1 / Plexin-A1 / Q9UIW2*ENSMUSG0000003008431
P70207 / Plxna2 / Plexin-A2 / O75051*ENSMUSG0000002664030
Plxna4 / Q80UG2 / plexin A4 / Q9HCM2*ENSMUSG0000002976530
P70208 / Plxna3 / plexin A3 / P51805*ENSMUSG0000003139828
Plxnc1 / Q9QZC2 / Plexin-C1 / O60486*ENSMUSG0000007478527


Protein motifs (from Interpro)
Interpro ID Name
 IPR001627  Sema domain
 IPR002165  Plexin repeat
 IPR002909  IPT domain
 IPR008936  Rho GTPase activation protein
 IPR013548  Plexin, cytoplasmic RasGAP domain
 IPR013783  Immunoglobulin-like fold
 IPR014756  Immunoglobulin E-set
 IPR015943  WD40/YVTN repeat-like-containing domain superfamily
 IPR016201  PSI domain
 IPR021157  Cytochrome c1, transmembrane anchor, C-terminal
 IPR031148  Plexin family
 IPR036352  Sema domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001525 angiogenesis IMP
 biological_processGO:0001569 branching involved in blood vessel morphogenesis IMP
 biological_processGO:0003151 outflow tract morphogenesis IMP
 biological_processGO:0003279 cardiac septum development IMP
 biological_processGO:0007162 negative regulation of cell adhesion IBA
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0007416 synapse assembly IMP
 biological_processGO:0008360 regulation of cell shape IBA
 biological_processGO:0030334 regulation of cell migration IMP
 biological_processGO:0032092 positive regulation of protein binding IDA
 biological_processGO:0035904 aorta development IMP
 biological_processGO:0043087 regulation of GTPase activity IBA
 biological_processGO:0043542 endothelial cell migration IMP
 biological_processGO:0045765 regulation of angiogenesis IMP
 biological_processGO:0050772 positive regulation of axonogenesis IBA
 biological_processGO:0060666 dichotomous subdivision of terminal units involved in salivary gland branching IDA
 biological_processGO:0060976 coronary vasculature development IMP
 biological_processGO:0071526 semaphorin-plexin signaling pathway IEA
 cellular_componentGO:0005886 plasma membrane IC
 cellular_componentGO:0005887 integral component of plasma membrane IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0030027 lamellipodium IEA
 cellular_componentGO:0031258 lamellipodium membrane IEA
 cellular_componentGO:0042995 cell projection IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0017154 semaphorin receptor activity IEA
 molecular_functionGO:0019904 protein domain specific binding IEA


Pathways (from Reactome)
Pathway description
Other semaphorin interactions


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000111 cleft palate "congenital fissure of the tissues normally uniting to form the palate" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
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Allelic Composition: Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi,Tg(Amh-cre)8815Reb/0,Tg(RARE-Hspa1b/lacZ)12Jrt/0,Tg(Stra8-icre)1Reb/0
Genetic Background: involves: C57BL/6 * C57BL/6N * CD-1 * FVB/N * SJL

Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0000141 abnormal vertebral body morphology "malformed main portion of the vertebra anterior to the vertebral canal" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:55583]
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Allelic Composition: Cenpetm1Dwc/Cenpetm2Dwc
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Plxnd1tm1Joe/Plxnd1tm1Joe
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0000154 rib fusion "appearance of one or more ribs as a single structure" [J:62022, J:62023]
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Allelic Composition: Cenpetm1Dwc/Cenpetm2Dwc
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0000272 abnormal aorta morphology "structural anomaly of the main trunk of the systemic arteries" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Cenpetm1Dwc/Cenpetm2Dwc
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0000284 double outlet right ventricle "both the aorta and the pulmonary trunk originate from the right ventricle, usually in conjunction with a ventricular septal defect" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:67826]
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Allelic Composition: Ccdc39b2b1304Clo/Ccdc39b2b1304Clo
Genetic Background: C57BL/6J-Ccdc39b2b1304Clo

Allelic Composition: Plxnd1b2b1863Clo/Plxnd1b2b1863Clo
Genetic Background: C57BL/6J-Plxnd1b2b1863Clo

 MP:0000445 short snout "reduced length of the anterior facial part of the muzzle" [J:53370]
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Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0000520 absent kidney "missing paired organs that excrete urine" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49471]
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Allelic Composition: Ccdc39b2b1304Clo/Ccdc39b2b1304Clo
Genetic Background: C57BL/6J-Ccdc39b2b1304Clo

Allelic Composition: Plxnd1b2b1863Clo/Plxnd1b2b1863Clo
Genetic Background: C57BL/6J-Plxnd1b2b1863Clo

Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0000592 short tail "reduced length of tail compared to control " [J:55583]
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Allelic Composition: Cenpetm1Dwc/Cenpetm2Dwc
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0000937 abnormal motor neuron morphology "malformation or absence of cells that innervate an effector (muscle or glandular) tissue; responsible for transmission of motor impulses" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:60159]
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Allelic Composition: Rasgrf1tm1Toc/Rasgrf1tm1Toc
Genetic Background: involves: 129/Sv

 MP:0000940 abnormal motor neuron innervation "misprojection or failure to bundle motor axons to an effector tissue" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:60159]
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Allelic Composition: Rasgrf1tm1Toc/Rasgrf1tm1Toc
Genetic Background: involves: 129/Sv

 MP:0001255 decreased body height "decreased shoulder to floor distance compared to controls" [dlb:Donna Burkart, Mouse Genome Informatics Curator]
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Allelic Composition: Cenpetm1Dwc/Cenpetm2Dwc
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0001575 cyanosis "a dark bluish or purple skin discoloration resulting from deficient oxygenation of the blood" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60159]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0001614 abnormal vasculature "anomalies in the structure of development of the network of tubes that carries blood through the body" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Cenpetm1Dwc/Cenpetm2Dwc
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0001823 thymus hypoplasia "small size due to reduced cell number in the thymus" [J:23255]
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Allelic Composition: Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi,Tg(Amh-cre)8815Reb/0,Tg(RARE-Hspa1b/lacZ)12Jrt/0,Tg(Stra8-icre)1Reb/0
Genetic Background: involves: C57BL/6 * C57BL/6N * CD-1 * FVB/N * SJL

Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0001914 hemorrhage "loss of blood from the vascular compartment to the exterior or into nonvascular body space as a result of rupture or severance of the blood vessels" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA

 MP:0001915 intracranial hemorrhage "bleeding within the skull, including hemorrhage into the brain and within the cranial epidural, subdural, and subarachnoid spaces" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Adgra2tm1.1Vlcg/Adgra2tm2.1Vlcg,Gt(ROSA)26Sortm3.1(cre/ERT2)Vlcg/Gt(ROSA)26Sor+
Genetic Background: involves: 129S6/SvEvTac * C57BL/6NTac

 MP:0002191 abnormal artery morphology "malformation of the blood vessels that carry blood away from the heart" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0002633 persistent truncus arteriosis "complete failure of the common arterial trunk opening out of both ventricles to divide into the aorta and pulmonary artery during development" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

Allelic Composition: Plxnd1b2b553Clo/Plxnd1b2b553Clo
Genetic Background: C57BL/6J-Plxnd1b2b553Clo

Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0002639 micrognathia "abnormally reduced size of the jaws, especially of the mandible" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0002792 abnormal retinal vascularization "malformation or disorganization of the blood vessels supplying the retina" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA

 MP:0002912 abnormal excitatory postsynaptic potential "defect in the potential detected in postsynaptic cells when an excitatory impulse arrives at the synapse causing depolarization" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Mapttm1(Sema3e)Yuyo/Mapt+,Olig2tm1(cre)Tmj/Olig2+
Genetic Background: Not Specified

 MP:0003057 abnormal epicardium morphology "anomalous structure of the visceral layer of the pericardium that surrounds and attaches to all the surfaces of the heart" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8, ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0003105 abnormal heart atrium morphology "structural anomaly of one or both of the two upper chambers of the heart " [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0003140 dilated atria "an expansion in the volume of one or both of the upper chambers of the heart" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0003544 abnormal vascular endothelial cell migration "anomaly in the movement of endothelial cell or their precursors to the appropriate location in the body" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:95387]
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Allelic Composition: Plxnd1tm1Joe/Plxnd1tm1Joe
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA

 MP:0004158 right aortic arch "the aortic arch lies to the right of the trachea and esophagus; results from persistance of the entire right dorsal arch and involution of a segment of the left arch" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

Allelic Composition: Plxnd1b2b553Clo/Plxnd1b2b553Clo
Genetic Background: C57BL/6J-Plxnd1b2b553Clo

Allelic Composition: Plxnd1b2b1863Clo/Plxnd1b2b1863Clo
Genetic Background: C57BL/6J-Plxnd1b2b1863Clo

Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0004612 fusion of vertebral bodies "improper union of the main cylindrical portion of adjacent vertebra ventral to the vertebral canal" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

Allelic Composition: Plxnd1tm1Joe/Plxnd1tm1Joe
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0005329 abnormal cardiac muscle morphology "anomalous structure of the involuntary muscle comprising the myocardium " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0005592 abnormal vascular smooth muscle morphology "structural anomaly of the nonstriated, involuntary muscle tissue of the blood vessels" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0005601 increased angiogenesis "enhanced process of blood vessel formation and the subsequent remodeling process; does not refer to the initial establishment of the vascular network" [RGD:Rat Genome Database submission]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0005602 decreased angiogenesis "reduced process of blood vessel formation and the subsequent remodeling process; does not refer to the initial establishment of the vascular network" [RGD:Rat Genome Database submission]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA

 MP:0006063 abnormal inferior vena cava morphology "structural malformation in the principal vein draining blood from the lower portion of the body" [smb:Susan M Bello, Mouse Genome Informatics Curator, Taber s Cyclopedic Medical Dictionary:19th edition: ISBN N 0-8036-0655-99]
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Allelic Composition: Plxnd1b2b553Clo/Plxnd1b2b553Clo
Genetic Background: C57BL/6J-Plxnd1b2b553Clo

 MP:0006354 abnormal fourth branchial arch artery morphology "any structural anomaly of the vessels formed within the fourth pair of branchial arches in embryogenesis" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0006355 abnormal sixth branchial arch artery morphology "any structural anomaly of the vessels formed within the sixth pair of branchial arches in embryogenesis" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0008725 enlarged heart atrium "increased size of one or both of the two upper chambers of the heart, to which the blood returns from the circulation" [MESH:A07.541.358]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0009660 abnormal induced retinal neovascularization "any anomaly in the response to conditions which induce the pathological growth of vessels into the retina" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Gt(ROSA)26Sortm1(CAG-Rhoj,-EGFP)Auem/Gt(ROSA)26Sortm1(CAG-Rhoj,-EGFP)Auem,Tg(Tek-cre)#Rwng/0
Genetic Background: involves: C57BL/6 * CBA

 MP:0010402 ventricular septal defect "abnormal communications between the two lower chambers of the heart, including such defects in the perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular regions" [MESH:C14.240.400.560.540]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0010406 absent atrial septum "absence of the thin membranous structure between the two heart atria" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0010412 atrioventricular septal defect "defects in the thin membranous structure between the right atrium and left ventricle that arise from faulty development of the embryonic endocardial cushions; the spectrum ranges from a primum atrial septal defect and cleft mitral valve, known as a partial atrioventricular septal defect (partial AVSD), to defects of both the primum atrial septum and inlet ventricular septum and the presence of a common atrioventricular valve, referred to as complete atrioventricular septal defect (complete AVSD)" [http://emedicine.medscape.com]
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Allelic Composition: Plxnd1b2b1863Clo/Plxnd1b2b1863Clo
Genetic Background: C57BL/6J-Plxnd1b2b1863Clo

Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0010413 complete atrioventricular septal defect "a type of atrioventricular septal defect in which a single atrioventricular valve annulus, a common atrioventricular valve, and a defect of the inlet ventricular septum are observed; deficiency of the atrioventricular septum also results in the presence of a large primum atrial septal defect" [http://emedicine.medscape.com]
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Allelic Composition: Plxnd1b2b553Clo/Plxnd1b2b553Clo
Genetic Background: C57BL/6J-Plxnd1b2b553Clo

 MP:0010454 abnormal truncus arteriosis septation "anomaly in the process of dividing the common arterial trunk arising out of both heart ventricles to divide into the aorta and pulmonary artery during development" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0010465 aberrant origin of the right subclavian artery "the right subclavian artery arises from an atypical location on the aortic arch or the proximal descending aorta" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0010466 vascular ring "the trachea and esophagus are completely encircled by connected segments of the aortic arch and its branches" [http://emedicine.medscape.com]
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Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0010472 abnormal ascending aorta and coronary artery attachment "any anomaly of the connection site of any or all of the coronary arteries to the ascending aorta" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0010488 abnormal left subclavian artery morphology "any structural anomaly of the artery that extends from the aortic arch to the left side of the body" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

Allelic Composition: Plxnd1b2b3150Clo/Plxnd1b2b3150Clo
Genetic Background: C57BL/6J-Plxnd1b2b3150Clo

 MP:0010551 abnormal coronary vessel morphology "any structural anomaly of any of the arteries or veins that supply blood to the heart or return blood from the heart muscles to the circulation" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0010565 absent fetal ductus arteriosus "absence of the fetal vessel that connects the left pulmonary artery with the descending aorta" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0011085 complete postnatal lethality "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0011087 complete neonatal lethality "death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

 MP:0011088 partial neonatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the neonatal period after birth (Mus: P0)" [MGI:csmith]
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Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

 MP:0011661 persistent truncus arteriosus type i "complete failure of the common arterial trunk opening out of both ventricles to divide into the aorta and pulmonary artery during development; type i is characterized by origin of a single pulmonary trunk from the left lateral aspect of the common trunk, with branching of the left and right pulmonary arteries from the pulmonary trunk" [http://emedicine.medscape.com]
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Allelic Composition: Plxnd1b2b553Clo/Plxnd1b2b553Clo
Genetic Background: C57BL/6J-Plxnd1b2b553Clo

 MP:0011662 persistent truncus arteriosus type ii "complete failure of the common arterial trunk opening out of both ventricles to divide into the aorta and pulmonary artery during development; type II is characterized by separate but proximate origins of the left and right pulmonary arterial branches from the posterolateral aspect of the common arterial trunk" [http://emedicine.medscape.com]
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Allelic Composition: Plxnd1b2b553Clo/Plxnd1b2b553Clo
Genetic Background: C57BL/6J-Plxnd1b2b553Clo

Allelic Composition: Plxnd1b2b1863Clo/Plxnd1b2b1863Clo
Genetic Background: C57BL/6J-Plxnd1b2b1863Clo

 MP:0011681 atrium cysts "abnormal membranous sacs in any portion of the paired upper chambers of the heart" [MGI:csmith]
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Allelic Composition: Plxnd1b2b553Clo/Plxnd1b2b553Clo
Genetic Background: C57BL/6J-Plxnd1b2b553Clo

 MP:0011682 renal glomerulus cysts "abnormal membranous sacs in any portion of the renal glomerulus" [MGI:csmith]
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Allelic Composition: Plxnd1b2b553Clo/Plxnd1b2b553Clo
Genetic Background: C57BL/6J-Plxnd1b2b553Clo

 MP:0011683 dual inferior vena cava "presence of two inferior vena cavae, often resulting from the persistence of both supracardinal veins during development; the two structures may be symmetric or asymmetric but typically join together at the renal vein" [MGI:csmith, PMID:10835118]
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Allelic Composition: Plxnd1b2b553Clo/Plxnd1b2b553Clo
Genetic Background: C57BL/6J-Plxnd1b2b553Clo

Allelic Composition: Plxnd1b2b1863Clo/Plxnd1b2b1863Clo
Genetic Background: C57BL/6J-Plxnd1b2b1863Clo

 MP:0012253 abnormal intersomitic vessel morphology "any structural anomaly of the primary blood vessel sprouts that originate from the dorsal aorta and posterior cardinal vein and align dorsoventrally at the myotomal boundaries between somites" [MGI:anna]
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Allelic Composition: Cux1tm1Mbu/Cux1tm1Mbu
Genetic Background: involves: OF1

Allelic Composition: Plxnd1tm1Ddg/Plxnd1tm1Ddg
Genetic Background: involves: 129S/SvEv * C57BL/6J

Allelic Composition: Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj,Tg(Tek-cre)1Ywa/0
Genetic Background: involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000063531 P70275 / Sema3e / sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E / O15041* / semaphorin 3E*  / complex / reaction
 ENSMUSG00000028064 Q62178 / Sema4a / Semaphorin-4A / Q9H3S1*  / reaction / complex






 

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