ENSMUSG00000042453


Mus musculus

Features
Gene ID: ENSMUSG00000042453
  
Biological name :Reln
  
Synonyms : Q60841 / Reelin / Reln
  
Possible biological names infered from orthology : P78509
  
Species: Mus musculus
  
Chr. number: 5
Strand: -1
Band: A3
Gene start: 21884454
Gene end: 22344702
  
Corresponding Affymetrix probe sets: 10528385 (MoGene1.0st)   1449465_at (Mouse Genome 430 2.0 Array)   1458020_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000058025
Ensembl peptide - ENSMUSP00000124052
Ensembl peptide - ENSMUSP00000124077
NCBI entrez gene - 19699     See in Manteia.
MGI - MGI:103022
RefSeq - NM_001310464
RefSeq - NM_011261
RefSeq Peptide - NP_001297393
RefSeq Peptide - NP_035391
swissprot - F6U2B2
swissprot - Q60841
Ensembl - ENSMUSG00000042453
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 CABZ01113373.1ENSDARG00000110545Danio rerio
 RELNENSGALG00000008193Gallus gallus
 RELNENSG00000189056Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR000742  EGF-like domain
 IPR002861  Reeler domain
 IPR008979  Galactose-binding-like domain superfamily
 IPR013032  EGF-like, conserved site
 IPR034968  Reelin
 IPR036278  Sialidase superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000904 cell morphogenesis involved in differentiation IMP
 biological_processGO:0001764 neuron migration IMP
 biological_processGO:0006508 proteolysis IEA
 biological_processGO:0007155 cell adhesion IEA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0007411 axon guidance IMP
 biological_processGO:0007417 central nervous system development IMP
 biological_processGO:0007420 brain development IMP
 biological_processGO:0007612 learning IMP
 biological_processGO:0007616 long-term memory IMP
 biological_processGO:0008306 associative learning IMP
 biological_processGO:0010001 glial cell differentiation IMP
 biological_processGO:0010468 regulation of gene expression IMP
 biological_processGO:0010976 positive regulation of neuron projection development IMP
 biological_processGO:0014068 positive regulation of phosphatidylinositol 3-kinase signaling IDA
 biological_processGO:0016358 dendrite development IMP
 biological_processGO:0016477 cell migration IMP
 biological_processGO:0018108 peptidyl-tyrosine phosphorylation IDA
 biological_processGO:0021511 spinal cord patterning IMP
 biological_processGO:0021517 ventral spinal cord development IEP
 biological_processGO:0021766 hippocampus development IDA
 biological_processGO:0021800 cerebral cortex tangential migration IMP
 biological_processGO:0021819 layer formation in cerebral cortex IMP
 biological_processGO:0021987 cerebral cortex development IMP
 biological_processGO:0030900 forebrain development IMP
 biological_processGO:0032008 positive regulation of TOR signaling IDA
 biological_processGO:0032793 positive regulation of CREB transcription factor activity IMP
 biological_processGO:0035418 protein localization to synapse IMP
 biological_processGO:0038026 reelin-mediated signaling pathway IDA
 biological_processGO:0045860 positive regulation of protein kinase activity IGI
 biological_processGO:0048265 response to pain IMP
 biological_processGO:0050731 positive regulation of peptidyl-tyrosine phosphorylation IDA
 biological_processGO:0050795 regulation of behavior IMP
 biological_processGO:0050804 modulation of chemical synaptic transmission IMP
 biological_processGO:0051057 positive regulation of small GTPase mediated signal transduction IDA
 biological_processGO:0051968 positive regulation of synaptic transmission, glutamatergic IMP
 biological_processGO:0060291 long-term synaptic potentiation IMP
 biological_processGO:0061003 positive regulation of dendritic spine morphogenesis IDA
 biological_processGO:0061098 positive regulation of protein tyrosine kinase activity IMP
 biological_processGO:0090129 positive regulation of synapse maturation IMP
 biological_processGO:0097107 postsynaptic density assembly IC
 biological_processGO:0097114 NMDA glutamate receptor clustering IMP
 biological_processGO:0097119 postsynaptic density protein 95 clustering IMP
 biological_processGO:0097120 receptor localization to synapse IMP
 biological_processGO:0097477 lateral motor column neuron migration IMP
 biological_processGO:1900273 positive regulation of long-term synaptic potentiation IDA
 biological_processGO:1902078 positive regulation of lateral motor column neuron migration IMP
 biological_processGO:2000310 regulation of NMDA receptor activity IMP
 biological_processGO:2000463 positive regulation of excitatory postsynaptic potential IMP
 biological_processGO:2000969 positive regulation of AMPA receptor activity IMP
 cellular_componentGO:0005576 extracellular region IEA
 cellular_componentGO:0005615 extracellular space IDA
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0030425 dendrite IDA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008233 peptidase activity IEA
 molecular_functionGO:0008236 serine-type peptidase activity IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0070325 lipoprotein particle receptor binding IPI
 molecular_functionGO:0070326 very-low-density lipoprotein particle receptor binding IPI


Pathways (from Reactome)
Pathway description
Reelin signalling pathway


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000743 muscle spasms "muscular twitching, cramps and seizures ; frequently associated with calcium deficiency, hypoparathyroidism, vitamin D deficiency or alkalosis " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: S1pr1tm1Rlp/S1pr1tm1Rlp
Genetic Background: involves: 129S6/SvEvTac

 MP:0000745 tremors "repetitive, cyclical movements of the body or a body part; usually involuntary, but can also manifest in response to an attempt at movement" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

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

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-od/Relnrl-od
Genetic Background: involves: C57BL/6 * DBA/2

Allelic Composition: Relnrl-tg/Relnrl-tg
Genetic Background: involves: C3H * C57BL/6 * DBA/2

Allelic Composition: Relnrl-Alb2/Relnrl-Alb2
Genetic Background: involves: C3H/HeJ * C57BL/6J

Allelic Composition: Relnrl-Alb/Relnrl-Alb
Genetic Background: involves: 101 * C3Hf/Rl

 MP:0000788 abnormal cerebral cortex morphology "malformed gray cellular mantle covering the surface of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:38857]
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Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm
Genetic Background: C.129S2(B6)-Cxcr2tm1Mwm/J

Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl-7J/Relnrl-7J
Genetic Background: C57BL/6J-Relnrl-7J/GrsrJ

Allelic Composition: Relnrl-8J/Relnrl-8J
Genetic Background: STOCK Relnrl-8J/J

Allelic Composition: Relntm1.1Mhat/Relntm1.1Mhat
Genetic Background: B6NSlc.B6(Cg)-Relntm1.1Mhat

 MP:0000790 abnormal stratification in cerebral cortex "abnormal formation or pattern of the layers of the cerebral cortex " [J:64289, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Relnrl-5J/Relnrl-5J
Genetic Background: C3Fe(SWV) Mbpshi-Relnrl-5J/GrsrJ

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

Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl-7J/Relnrl-7J
Genetic Background: C57BL/6J-Relnrl-7J/GrsrJ

Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

Allelic Composition: Relnrl-od/Relnrl-od
Genetic Background: involves: C57BL/6 * DBA/2

Allelic Composition: Relnctrdel/Relnctrdel,Rgs4tm1Dgen/Rgs4+
Genetic Background: involves: 129P2/OlaHsd * A/J * C57BL/6

 MP:0000792 abnormal cortical marginal zone morphology 
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Allelic Composition: Rag2tm1.1Cgn/Rag2tm1.1Cgn
Genetic Background: C57BL/6-Rag2tm1.1Cgn

Allelic Composition: Dab1tm1Cpr/Dab1tm4Cpr,Relnrl/Reln+
Genetic Background: involves: 129/Sv * C3HeB/Fe * C57BL/6

Allelic Composition: Relnrl-5J/Relnrl-5J
Genetic Background: C3Fe(SWV) Mbpshi-Relnrl-5J/GrsrJ

Allelic Composition: Relntm1.1Mhat/Relntm1.1Mhat
Genetic Background: B6NSlc.B6(Cg)-Relntm1.1Mhat

 MP:0000807 abnormal hippocampus morphology "absent or malformed deep lying structure of the cerebrum involved with memory storage and spatial navigation" [The Atlas of Mouse Development:ISBN 0-12-402035-6, MGI:Cls, J:38857]
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Allelic Composition: Msx1tm1Rilm/Msx1tm1Rilm,Msx2tm1Rilm/Msx2tm1Rilm
Genetic Background: involves: 129S4/SvJae * BALB/c * CD-1

Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-7J/Relnrl-7J
Genetic Background: C57BL/6J-Relnrl-7J/GrsrJ

Allelic Composition: Relnrl-od/Relnrl-od
Genetic Background: involves: C57BL/6 * DBA/2

Allelic Composition: Relnrl-8J/Relnrl-8J
Genetic Background: STOCK Relnrl-8J/J

Allelic Composition: Relntm1.1Mhat/Relntm1.1Mhat
Genetic Background: B6NSlc.B6(Cg)-Relntm1.1Mhat

 MP:0000812 abnormal dentate gyrus morphology "absence or malformation of one of two interlocking gyri of the hippocampus that contains granule cells, which project to the pyramidal cells and interneurons of the CA3 region of the ammon gyrus" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:38857]
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Allelic Composition: Rag2tm1.1Cgn/Rag2tm1.1Cgn
Genetic Background: C57BL/6-Rag2tm1.1Cgn

Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-od/Relnrl-od
Genetic Background: involves: C57BL/6 * DBA/2

Allelic Composition: Relnrl-8J/Relnrl-8J
Genetic Background: STOCK Relnrl-8J/J

Allelic Composition: Relntm1.1Mhat/Relntm1.1Mhat
Genetic Background: B6NSlc.B6(Cg)-Relntm1.1Mhat

 MP:0000813 abnormal hippocampal laminar structure "malformed or missing layers of the laminar structure of the hippocampus" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:38857]
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Allelic Composition: Relnrl-5J/Relnrl-5J
Genetic Background: C3Fe(SWV) Mbpshi-Relnrl-5J/GrsrJ

Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

 MP:0000819 abnormal olfactory bulb morphology "malformation or absence of the forebrain region that coordinates neuronal signaling involved in the perception of smell; it receives input from the sensory neurons and outputs to the olfactory cortex" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, Principles of Neural Science:ISBN 0-8385-8034-3, J:16461]
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Allelic Composition: Dab1tm1Cpr/Dab1tm1Cpr
Genetic Background: either: (involves: 129S4/SvJaeSor * BALB/c) or (involves: 129S4/SvJaeSor * C57BL/6)

 MP:0000849 abnormal cerebellum morphology "any malformation or absence of the part of the metencephalon that lies in the posterior cranial fossa dorsal to the pons and medulla that is concerned with the coordination of movement and learning of motor skills" [J:50311, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm
Genetic Background: C.129S2(B6)-Cxcr2tm1Mwm/J

 MP:0000852 small cerebellum "reduced size of cerebellum" [MGI:CLS, J:17203, J:67524]
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Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm
Genetic Background: C.129S2(B6)-Cxcr2tm1Mwm/J

Allelic Composition: Relnrl-5J/Relnrl-5J
Genetic Background: C3Fe(SWV) Mbpshi-Relnrl-5J/GrsrJ

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

Allelic Composition: Relnrl/Reln+
Genetic Background: involves: BALB/c

Allelic Composition: Relnrl-7J/Relnrl-7J
Genetic Background: C57BL/6J-Relnrl-7J/GrsrJ

Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

Allelic Composition: Relnrl-8J/Relnrl-8J
Genetic Background: STOCK Relnrl-8J/J

Allelic Composition: Relnrl-tg/Relnrl-tg
Genetic Background: involves: C3H * C57BL/6 * DBA/2

Allelic Composition: Relnrl-Alb/Relnrl-Alb
Genetic Background: involves: 101 * C3Hf/Rl

 MP:0000853 absent cerebellar foliation "missing small branches of the cerebellar lobules" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3, tc:Teresa Chu , Mouse Genome Informatics Curator, J:60896]
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Allelic Composition: Relnrl-tg/Relnrl-tg
Genetic Background: involves: C3H * C57BL/6 * DBA/2

 MP:0000854 abnormal cerebellum development "malformed or incomplete differentiation of the part of the metencephalon that lies dorsal to the pons and medulla behind the brain stem and controls balance for walking and standing, modulates the force and range of movement and is involved in the learning of motor skills " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Relnrl-6J/Relnrl-6J
Genetic Background: C57BL/6J-Relnrl-6J/J

 MP:0000872 abnormal external granule cell layer "malformation of the transient layer of the cerebellar cortex which is composed of the dividing and migrating granule cells" [tc:Teresa Chu , Mouse Genome Informatics Curator]
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Allelic Composition: Relnrl-Alb/Relnrl-Alb
Genetic Background: involves: 101 * C3Hf/Rl

 MP:0000875 abnormal cerebellar Purkinje cell layer "any malformation or absence of the cell layer that lies just underneath the molecular layer of the cerebellar cortex; it contains the neuronal cell bodies of the Purkinje cells that are arranged side by side in a single layer, and candelabrum interneurons are vertically oriented between the Purkinje cells" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Relnrl-7J/Relnrl-7J
Genetic Background: C57BL/6J-Relnrl-7J/GrsrJ

Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

Allelic Composition: Relnrl-od/Relnrl-od
Genetic Background: involves: C57BL/6 * DBA/2

 MP:0000876 Purkinje cell degeneration "a retrogressive impairment of function or destruction of the large neurons located at the interface of the molecular and internal granule layers of the cerebellar cortex" [J:46854]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0000877 abnormal Purkinje cell "any structural anomaly of the neurons located at the interface of the molecular and internal granule layers of the cerebellar cortex; these inhibitory neurons provide the output of the cerebellar cortex through axons that project into the white matter, and extensive dendritic trees from the Purkinje cells extend upward in a single plane into the molecular layer where they synapse with parallel fibers of granule cells" [J:46140, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Relnrl-Alb/Relnrl-Alb
Genetic Background: involves: 101 * C3Hf/Rl

 MP:0000880 decreased Purkinje cell number "fewer than normal neuronal cells that are located in the interface of the molecular and granular layers of the cerebellar cortex" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:45302]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Relnrl-Alb/Relnrl-Alb
Genetic Background: involves: 101 * C3Hf/Rl

 MP:0000884 delaminated Purkinje cell layer "splitting or disorganization of the layer of large neuron cell bodies between the molecular and granular layers of the cerebellum" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61509]
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Allelic Composition: Relnrl-5J/Relnrl-5J
Genetic Background: C3Fe(SWV) Mbpshi-Relnrl-5J/GrsrJ

 MP:0000885 ectopic Purkinje cell "Purkinje cell body resides in places other than the Purkinje cell layer in the cerebellum" [MGI:tc, J:60896]
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Allelic Composition: Relnrl-Alb/Relnrl-Alb
Genetic Background: involves: 101 * C3Hf/Rl

 MP:0000886 abnormal cerebellar granule layer "any malformation or absence of the innermost cortical layer of the cerebellum; contains densly packed small neurons, mostly granule cells with some Golgi cells are found at the outer border" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

 MP:0000887 delaminated granule layer "splitting or disorganization of the deepest of the three layers of the cerebellum that contains granule cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61509]
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Allelic Composition: Relnrl-5J/Relnrl-5J
Genetic Background: C3Fe(SWV) Mbpshi-Relnrl-5J/GrsrJ

 MP:0000968 abnormal sensory neuron innervation "defective or incomplete supply of nerve fibers to sensory termini or to spinal cord" [J:31622]
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Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
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Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-od/Relnrl-od
Genetic Background: involves: C57BL/6 * DBA/2

 MP:0001265 reduced body size "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

Allelic Composition: Relnrl-Alb/Relnrl-Alb
Genetic Background: involves: 101 * C3Hf/Rl

Allelic Composition: Relnm1Anu/Relnm1Anu
Genetic Background: C57BL/6JAnu-Relnm1Anu

 MP:0001360 abnormal social investigation "altered behavior of animals to approach and examine other animals" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Meis1tm1Mtor/Meis1tm1Mtor
Genetic Background: Not Specified

 MP:0001393 ataxia "inability to coordinate voluntary muscular movements" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:67231]
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Allelic Composition: Agtpbp1pcd-7J/Agtpbp1pcd-7J
Genetic Background: C.Cg-Igh-6tm1Cgn Agtpbp1pcd-7J

Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-7J/Relnrl-7J
Genetic Background: C57BL/6J-Relnrl-7J/GrsrJ

Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

Allelic Composition: Relnrl-od/Relnrl-od
Genetic Background: involves: C57BL/6 * DBA/2

Allelic Composition: Relnrl-8J/Relnrl-8J
Genetic Background: STOCK Relnrl-8J/J

Allelic Composition: Relnrl-tg/Relnrl-tg
Genetic Background: involves: C3H * C57BL/6 * DBA/2

Allelic Composition: Relnrl-Alb/Relnrl-Alb
Genetic Background: involves: 101 * C3Hf/Rl

 MP:0001402 hypoactivity "reduced movement from one place to another" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:64289]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-od/Relnrl-od
Genetic Background: involves: C57BL/6 * DBA/2

 MP:0001405 impaired coordination "reduced ability to execute integrated movements of muscle" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Relnm1Anu/Relnm1Anu
Genetic Background: C57BL/6JAnu-Relnm1Anu

 MP:0001406 abnormal gait "unusual or distinctive way of walking" [J:65038]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-7J/Relnrl-7J
Genetic Background: C57BL/6J-Relnrl-7J/GrsrJ

Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

Allelic Composition: Relnrl-8J/Relnrl-8J
Genetic Background: STOCK Relnrl-8J/J

Allelic Composition: Relnrl-tg/Relnrl-tg
Genetic Background: involves: C3H * C57BL/6 * DBA/2

 MP:0001504 abnormal posture "atypical position of the limbs or carriage of the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:18984]
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Allelic Composition: Htr2ctm1Knk/Htr2ctm2Knk
Genetic Background: B6.Cg-Htr2ctm1Knk/Htr2ctm2Knk

 MP:0001511 disheveled coat "coat that looks generally unkempt" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

 MP:0001516 abnormal motor coordination/ balance "altered ability of an animal to maintain skillful and effective interaction of movements or maintenance of equilibrium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Igf2rtm1Arge/Igf2r+
Genetic Background: involves: 129/Sv * 129P2/OlaHsd * 129S/SvEv

 MP:0001523 impaired righting response "reduced ability or greater amount of time needed to recover from supine position" [J:25565]
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Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-8J/Relnrl-8J
Genetic Background: STOCK Relnrl-8J/J

Allelic Composition: Relnrl-Alb2/Relnrl-Alb2
Genetic Background: involves: C3H/HeJ * C57BL/6J

 MP:0001525 impaired balance "reduced ability of an animal to maintain equilibrium" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:64962, J:17123]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

Allelic Composition: Relnrl-7J/Relnrl-7J
Genetic Background: C57BL/6J-Relnrl-7J/GrsrJ

Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

 MP:0001732 postnatal growth retardation "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-od/Relnrl-od
Genetic Background: involves: C57BL/6 * DBA/2

 MP:0001923 reduced female fertility "reduced ability of female to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

 MP:0001924 infertility "inability to produce live offspring" [J:47225]
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Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

 MP:0001925 male infertility "inability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

 MP:0002066 abnormal motor capabilities/coordination/movement "altered ability to coordinate voluntary movement or repetitive, compulsive movements" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 MP:0002082 postnatal lethality "premature death anytime after postnatal day 1 to weaning age (3 weeks)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Igf2rtm1Arge/Igf2r+
Genetic Background: involves: 129/Sv * 129P2/OlaHsd * 129S/SvEv

 MP:0002083 premature death "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Klf2tm1Jml/Klf2tm1Jml
Genetic Background: either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * C57BL/6 * CD-1)

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relnrl-7J/Relnrl-7J
Genetic Background: C57BL/6J-Relnrl-7J/GrsrJ

Allelic Composition: Relnrl-8J/Relnrl-8J
Genetic Background: STOCK Relnrl-8J/J

 MP:0002566 abnormal sexual interaction "altered initiation, failure of initiation or incomplete mating behavior" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Agtpbp1pcd/Agtpbp1pcd
Genetic Background: involves: C57BR/cdJ

 MP:0003088 abnormal prepulse inhibition "increase or decrease in the ability of a relatively mild stimulus to suppress the response to a strong, startle-eliciting stimulus" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:91131]
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Allelic Composition: Meis1tm1Mtor/Meis1tm1Mtor
Genetic Background: Not Specified

 MP:0003651 abnormal axon outgrowth "defect/abnormality in the ability of an axon to extend from a neuron cell body" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator, J:96121]
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Allelic Composition: Hspa5baffled/Hspa5baffled,Tg(Mbp-MAPT/lacZ)#aCaw/Tg(Mbp-MAPT/lacZ)#aCaw
Genetic Background: involves: BALB/c * C57BL/6 * C57BL/6J * FVB/N

 MP:0003733 abnormal inner nuclear layer morphology "malformation/anomalous structure of the retinal layer which contains the cell bodies of bipolar, horizontal, and amacrine cells" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Nudt1tm1Tts/Nudt1tm1Tts
Genetic Background: B6.129S-Nudt1tm1Tts

 MP:0004021 abnormal rod electrophysiology "anomaly in the function of dark adapted vision mediated by the rods" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Nudt1tm1Tts/Nudt1tm1Tts
Genetic Background: B6.129S-Nudt1tm1Tts

 MP:0004022 abnormal cone electrophysiology "anomaly in the function of light adapted vision mediated by the cones" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Nudt1tm1Tts/Nudt1tm1Tts
Genetic Background: B6.129S-Nudt1tm1Tts

 MP:0004097 abnormal cerebellar cortex morphology "any structural anomaly of the thin mantle of gray matter that covers the surface of each cerebral hemisphere, including the six layers of nerve cells and the nerve pathways that connect them; together, these regions are responsible for the processes of conscious thought, perception, emotion and memory as well as advanced motor function" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

Allelic Composition: Relnrl-8J/Relnrl-8J
Genetic Background: STOCK Relnrl-8J/J

Allelic Composition: Relnrl-tg/Relnrl-tg
Genetic Background: involves: C3H * C57BL/6 * DBA/2

 MP:0004103 abnormal ventral striatum morphology "any structural abnormality of the regions of the nucleus accumbens and some nuclei of the olfactory tubercule that lie ventral to the anterior commissure" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Adcy4tm1.1Dek/Adcy4tm1.1Dek,Tg(AQP2-cre)2Dek/0
Genetic Background: involves: C57BL/6 * CBA

 MP:0004275 abnormal postnatal subventricular zone morphology "any structural anomaly of the mitotically active layer of cells surrounding the brain ventricles in the adult that consists of migrating neuroblasts, astrocytes and transitory amplifying progenitor cells" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:12637172]
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Allelic Composition: Dab1tm1Cpr/Dab1tm1Cpr
Genetic Background: either: (involves: 129S4/SvJaeSor * BALB/c) or (involves: 129S4/SvJaeSor * C57BL/6)

 MP:0004279 abnormal rostral migratory stream morphology "any structural anomaly of the transient structure formed by neurons migrating from the subventricular zone into the olfactory bulbs" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Dab1tm1Cpr/Dab1tm1Cpr
Genetic Background: either: (involves: 129S4/SvJaeSor * BALB/c) or (involves: 129S4/SvJaeSor * C57BL/6)

 MP:0005036 diarrhea "abnormally frequent discharge of semi-solid or fluid fecal matter from the bowel" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

 MP:0005267 abnormal olfactory cortex morphology "anomalous structure of piriform cortex, part of the olfactory tract, which receives its major afferents from the olfactory bulb, and is primarily responsible for the identification of odors" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83884]
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Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

 MP:0006009 abnormal neuronal migration "defective or impaired movement of immature neurons from germinal zones to specific positions where they will reside as they mature" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

 MP:0006074 abnormal retinal rod bipolar cell morphology "anomalous structure of the bipolar cells that function in low light and transmit signals only through amacrine cells" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:92623]
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Allelic Composition: Nudt1tm1Tts/Nudt1tm1Tts
Genetic Background: B6.129S-Nudt1tm1Tts

 MP:0006300 abnormal entorhinal cortex morphology "any structural anomaly of the structure in the anterior parahippocampus that lies forward of the parahippocampal cortex and immediately medial to the perirhinal cortex, bounded superiorly by the hippocampus and inferiorly by the collateral sulcus" [brs:Beverly Richards-Smith_IMSR Curator]
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Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

 MP:0008031 decreased Cajal-Retzius cell number "reduced number of the distinct population of large, bipolar cells, distributed in a continuous band along the marginal zone of the cortex extending to the molecular layer of the dentate gyrus" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"]
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Allelic Composition: Gt(ROSA)26Sortm1(DTA)Riet/Gt(ROSA)26Sor+,Relnrl/Reln+,Trp73tm1(cre)Agof/Trp73+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ

Allelic Composition: Gt(ROSA)26Sortm1(DTA)Riet/Gt(ROSA)26Sor+,Relnrl/Reln+,Wnt3atm1(cre)Eag/Wnt3a+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ

Allelic Composition: Gt(ROSA)26Sortm1(DTA)Riet/Gt(ROSA)26Sor+,Relnrl/Reln+,Trp73tm1(cre)Agof/Trp73+,Wnt3atm1(cre)Eag/Wnt3a+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ

 MP:0008263 abnormal hippocampus CA1 region morphology 
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Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

Allelic Composition: Relntm1.1Mhat/Relntm1.1Mhat
Genetic Background: B6NSlc.B6(Cg)-Relntm1.1Mhat

 MP:0008265 abnormal hippocampus CA2 region morphology 
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Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

Allelic Composition: Relnrl/Relnrl
Genetic Background: B6.Cg-Relnrl

 MP:0008284 abnormal hippocampus pyramidal cell layer 
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Allelic Composition: Rag2tm1.1Cgn/Rag2tm1.1Cgn
Genetic Background: C57BL/6-Rag2tm1.1Cgn

Allelic Composition: Relnrl-tg/Relnrl-tg
Genetic Background: involves: C3H * C57BL/6 * DBA/2

 MP:0008285 abnormal hippocampus granule cell layer 
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Allelic Composition: Relnrl-tg/Relnrl-tg
Genetic Background: involves: C3H * C57BL/6 * DBA/2

 MP:0008431 abnormal short-term spatial reference memory "anomaly in the short-term memory for spatial location information that is established during the first few minutes after training or an encouter at that location" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Meis1tm1Mtor/Meis1tm1Mtor
Genetic Background: Not Specified

 MP:0008489 postnatal slow weight gain "the weight gain over a span of postnatal developmental time is slower than controls, with or without ever attaining a similar weight to controls as adults" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Relnrl/Relnrl
Genetic Background: C3.Cg-Relnrl

 MP:0008770 decreased survivor rate "a smaller percentage of organisms than expected survive to adulthood and have a lifespan similar to controls" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Relnrl-Alb/Relnrl-Alb
Genetic Background: involves: 101 * C3Hf/Rl

 MP:0009937 abnormal neuron differentiation "abnormal growth or development of the cells of the nervous system that receive, conduct, and transmit impulses" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Cxcr2tm1Mwm/Cxcr2tm1Mwm
Genetic Background: C.129S2(B6)-Cxcr2tm1Mwm/J

 MP:0009949 abnormal olfactory bulb granule cell layer morphology 
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Allelic Composition: Dab1tm1Cpr/Dab1tm1Cpr
Genetic Background: either: (involves: 129S4/SvJaeSor * BALB/c) or (involves: 129S4/SvJaeSor * C57BL/6)

 MP:0011083 complete lethality at weaning "premature death at weaning age of all organisms of a given genotype in a population, often due to the inability to make the transition to solid food" [MGI:csmith]
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Allelic Composition: Psen1tm1Vln/Psen1tm1Vln,Tg(Thy1-APPLon)2Vln/0,Tg(Thy1-cre)1Vln/0
Genetic Background: involves: FVB/N

 MP:0011086 partial postnatal 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 anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
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Allelic Composition: Relnrl-4J/Relnrl-4J
Genetic Background: B6.Cg-Relnrl-4J/GrsrJ

 MP:0011448 decreased dopaminergic neuron number "fewer than normal numbers of the neurons that utilize dopamine as a neurotransmitter" [MGI:smb]
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Allelic Composition: Adcy4tm1.1Dek/Adcy4tm1.1Dek,Tg(AQP2-cre)2Dek/0
Genetic Background: involves: C57BL/6 * CBA

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000024924 Vldlr / P98156 / very low density lipoprotein receptor / P98155*  / reaction / complex
 ENSMUSG00000028519 Dab1 / P97318 / Disabled homolog 1 / O75553* / DAB1, reelin adaptor protein*  / complex / reaction
 ENSMUSG00000019843 Fyn / P39688 / Tyrosine-protein kinase Fyn / P06241* / FYN proto-oncogene, Src family tyrosine kinase*  / reaction
 ENSMUSG00000040990 Q8R550 / Sh3kbp1 / SH3 domain-containing kinase-binding protein 1 / Q96B97*  / complex / reaction






 

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