ENSMUSG00000001089


Mus musculus

Features
Gene ID: ENSMUSG00000001089
  
Biological name :Luzp1
  
Synonyms : Leucine zipper protein 1 / Luzp1 / Q8R4U7
  
Possible biological names infered from orthology : Q86V48
  
Species: Mus musculus
  
Chr. number: 4
Strand: 1
Band: D3
Gene start: 136469761
Gene end: 136554780
  
Corresponding Affymetrix probe sets: 10509246 (MoGene1.0st)   1416469_at (Mouse Genome 430 2.0 Array)   1448352_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000130758
Ensembl peptide - ENSMUSP00000132089
Ensembl peptide - ENSMUSP00000001116
Ensembl peptide - ENSMUSP00000060619
Ensembl peptide - ENSMUSP00000101475
Ensembl peptide - ENSMUSP00000128591
NCBI entrez gene - 269593     See in Manteia.
MGI - MGI:107629
RefSeq - NM_024452
RefSeq - XM_006538921
RefSeq Peptide - NP_077772
swissprot - E9Q9L3
swissprot - Q8R4U7
swissprot - F6XG76
Ensembl - ENSMUSG00000001089
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 luzp1ENSDARG00000075556Danio rerio
 LUZP1ENSGALG00000025858Gallus gallus
 LUZP1ENSG00000169641Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Filip1 / Mus musculus filamin A interacting protein 1 (Filip1), transcript variant 3, mRNA. / Q7Z7B0* / filamin A interacting protein 1*ENSMUSG0000003489823
Q6P6L0 / Filip1l / Filamin A-interacting protein 1-like / Q4L180*ENSMUSG0000004333619


Protein motifs (from Interpro)
Interpro ID Name
 IPR026734  Leucine zipper protein 1


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0003281 ventricular septum development IMP
 biological_processGO:0021503 neural fold bending IMP
 biological_processGO:0060840 artery development IMP
 cellular_componentGO:0005634 nucleus IDA
 molecular_functionGO:0003674 molecular_function ND


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 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]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0000841 abnormal hindbrain morphology "malformed caudal region of the brain; includes cerebellum, pons and medulla oblongata" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:45302]
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Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0000848 abnormal pons "malformed band of nerve fibers in the brain connecting the medulla oblongata and the mesencephalon; this region conveys information about movement from the cerebral hemisphere to the cerebellum" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:1776, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0000914 exencephaly "neurocranial defects resulting in exposure or extrusion of the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
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Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0000923 abnormal roof plate morphology "malformation or absence of a transient group of neuroepithelial cells located at the dorsal midline of the neural tube that profoundly influences the development of the vertebrate central nervous system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0000928 incomplete cephalic closure "arrest of the fusion of the cephalic neural folds" [J:12622]
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Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 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]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0001890 anencephaly "absence of the bones of the cranial vault and absent or rudimentary cerebral and cerebellar hemispheres, brainstem, and basal ganglia" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:31571]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0003052 omphalocele "protrusion of abdominal viscera at the base of the umbilical cord, with a covering membranous sac of peritoneum-amnion" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8, MeSH:National Library of Medicine - Medical Subject Headings, 2003, ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0004110 transposition of great arteries "cardiovascular malformation in which the aorta arises from the right ventricle while the pulmonary artery arises from the left ventricle" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0009264 failure of eyelid fusion "the upper and lower thin folds of skin and muscle that cover the exposed portion of the eye do not fuse together during development" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0009888 palatal shelves fail to meet at midline "polarized growth towards the midline following palatal shelf elevation does not occur" [PMID:16942766]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0009890 cleft secondary palate "congenital fissure of the tissues normally uniting to form the secondary palate" [PMID:16680722]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 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]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0011089 complete perinatal lethality "death of all organisms of a given genotype in a population within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0011101 partial prenatal 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 between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0011256 abnormal neural fold morphology "any structural anomaly of the elevated margins of the neural groove" [ISBN:0-683-40008-8]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0011380 enlarged brain ventricle "increased size of one or more of the four communicating cavities within the brain that are continuous with the central canal of the spinal cord" [MGI:smb]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0012261 increased hindbrain apoptosis "increase in the number of cells of the hindbrain undergoing programmed cell death" [MGI:anna]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0012525 abnormal rhombic lip morphology "any structural anomaly of the posterior section of the developing metencephalon recognized transiently within the vertebrate embryo; the rhombic lip extends posteriorly from the roof of the fourth ventricle to dorsal neuroepithelial cell and can be divided into eight structural units based on rhombomeres 1-8 (r1-r8), recognized at early stages of hindbrain development; producing granule cells and five brainstem nuclei, the rhombic lip plays an important role in developing a complex cerebellar neural system" [MGI:anna]
Show

Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Fabp4-cre)1Abel/?
Genetic Background: involves: C57BL/6 * FVB/N

  


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






 

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