ENSMUSG00000025278


Mus musculus

Features
Gene ID: ENSMUSG00000025278
  
Biological name :Flnb
  
Synonyms : Filamin-B / Flnb / Q80X90
  
Possible biological names infered from orthology : O75369
  
Species: Mus musculus
  
Chr. number: 14
Strand: 1
Band: A1
Gene start: 7817957
Gene end: 7951588
  
Corresponding Affymetrix probe sets: 10412562 (MoGene1.0st)   1426750_at (Mouse Genome 430 2.0 Array)   1442107_at (Mouse Genome 430 2.0 Array)   1458226_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000052020
NCBI entrez gene - 286940     See in Manteia.
MGI - MGI:2446089
RefSeq - XM_006518050
RefSeq - NM_001081427
RefSeq - NM_134080
RefSeq Peptide - NP_598841
RefSeq Peptide - NP_001074896
swissprot - Q80X90
Ensembl - ENSMUSG00000025278
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 FP325130.1ENSDARG00000112527Danio rerio
 FLNBENSGALG00000005678Gallus gallus
 FLNBENSG00000136068Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Flnc / Q8VHX6 / Filamin-C / Q14315*ENSMUSG0000006869970
Flna / Q8BTM8 / Filamin-A / P21333*ENSMUSG0000003132869
Syne2 / Q6ZWQ0 / spectrin repeat containing, nuclear envelope 2 / Q8WXH0* / spectrin repeat containing nuclear envelope protein 2*ENSMUSG0000006345016
Clmn / Q8C5W0 / Calmin / Q96JQ2*ENSMUSG000000210977
Syne1 / Q6ZWR6 / Mus musculus spectrin repeat containing, nuclear envelope 1 (Syne1), transcript variant 5, mRNA. / Q8NF91* / spectrin repeat containing nuclear envelope protein 1*ENSMUSG000000960546


Protein motifs (from Interpro)
Interpro ID Name
 IPR001298  Filamin/ABP280 repeat
 IPR001589  Actinin-type actin-binding domain, conserved site
 IPR001715  Calponin homology domain
 IPR013783  Immunoglobulin-like fold
 IPR014756  Immunoglobulin E-set
 IPR017868  Filamin/ABP280 repeat-like
 IPR029874  Filamin-B
 IPR036872  CH domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0003334 keratinocyte development IMP
 biological_processGO:0003382 epithelial cell morphogenesis IMP
 biological_processGO:0007519 skeletal muscle tissue development IDA
 biological_processGO:0030036 actin cytoskeleton organization IMP
 biological_processGO:0030154 cell differentiation IEA
 biological_processGO:0071346 cellular response to interferon-gamma IDA
 cellular_componentGO:0001725 stress fiber IDA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol IEA
 cellular_componentGO:0005856 cytoskeleton IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0005903 brush border IDA
 cellular_componentGO:0005925 focal adhesion IDA
 cellular_componentGO:0005938 cell cortex IEA
 cellular_componentGO:0030018 Z disc IEA
 cellular_componentGO:0031012 extracellular matrix ISO
 cellular_componentGO:0043005 neuron projection IEA
 cellular_componentGO:0043025 neuronal cell body IEA
 cellular_componentGO:0045335 phagocytic vesicle IDA
 molecular_functionGO:0003779 actin binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0042802 identical protein binding IEA
 molecular_functionGO:0045296 cadherin binding IEA


Pathways (from Reactome)
Pathway description
ISG15 antiviral mechanism


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000060 delayed bone ossification "late onset of the formation of bone" [J:40203]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000063 reduced bone density "decreased mineral content of bone; indicator of bone strength" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:57315]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000069 kyphoscoliosis "kyphosis combined with scoliosis" [MGI:CML, J:66943]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0000074 abnormal neurocranium morphology "malformed bones of the skull enclosing the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:55583]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000109 abnormal parietal bone morphology "malformed curved bone forming part of the vault of the cranium" [J:17489]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000135 reduced cortical bone thickness "thinner than normal superficial layer of compact bone " [J:61509]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0000154 rib fusion "appearance of one or more ribs as a single structure" [J:62022, J:62023]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000157 abnormal sternum morphology "malformed long flat bone of the chest; articulates with clavicle and first seven rib pairs" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:19212]
Show

Allelic Composition: FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Flnbskm2/Flnbskm2
Genetic Background: involves: 129S1/SvImJ * 129X1/SvJ * DBA/2J

 MP:0000160 kyphosis "forward curvature of the spine, characterized by extensive flexion. " [J:62023, J:66943, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
Show

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000161 scoliosis "lateral and rotational curvature of the spine" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:53770, J:66943]
Show

Allelic Composition: FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Flnbskm2/Flnbskm2
Genetic Background: involves: 129S1/SvImJ * 129X1/SvJ * DBA/2J

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000162 lordosis "anteriorly convex curvature of the spine, "saddle back" " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:62022]
Show

Allelic Composition: Flnbskm2/Flnbskm2
Genetic Background: involves: 129S1/SvImJ * 129X1/SvJ * DBA/2J

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000166 abnormal chondrocyte morphology "anomalous structure, organization, or differentiation of nondividing cartilage cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:40203]
Show

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000260 abnormal angiogenesis "aberrant process of blood vessel formation and the subsequent remodeling process; does not refer to the initial establishment of the vascular network" [J:67296, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0000547 short limbs "reduced average length of the extremities" [MGI:CLS, J:61509]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0000552 abnormal radius morphology "malformation of the short bone of the lateral forearm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0001255 decreased body height "decreased shoulder to floor distance compared to controls" [dlb:Donna Burkart, Mouse Genome Informatics Curator]
Show

Allelic Composition: Hmox1tm1.1Hes/Hmox1tm1.1Hes,Lyz2tm1(cre)Ifo/Lyz2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

Allelic Composition: FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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]
Show

Allelic Composition: Cftrtm1Unc/Cftr+
Genetic Background: involves: BALB/cJ * C57BL/6J

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001406 abnormal gait "unusual or distinctive way of walking" [J:65038]
Show

Allelic Composition: Hmox1tm1.1Hes/Hmox1tm1.1Hes,Lyz2tm1(cre)Ifo/Lyz2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N

 MP:0001429 dehydration "excessive water loss from the body or from an organ or bodily part" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:50053]
Show

Allelic Composition: Hmox1tm1.1Hes/Hmox1tm1.1Hes,Lyz2tm1(cre)Ifo/Lyz2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N

 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]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001732 postnatal growth retardation "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 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]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0002083 premature death "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0002113 abnormal skeleton development "anomalous differentiation or remodeling of bone tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: IL-23RIl23rtm1.1Ngh/IL-23RIl23rtm1.1Ngh,Rag2tm1Fwa/Rag2tm1Fwa
Genetic Background: involves: 129S/SvEv * C57BL/6

 MP:0002115 abnormal skeleton extremities morphology "abnormal development of limb, foot or tail bones resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: IL-23RIl23rtm1.1Ngh/IL-23RIl23rtm1.1Ngh,Rag2tm1Fwa/Rag2tm1Fwa
Genetic Background: involves: 129S/SvEv * C57BL/6

 MP:0002543 brachyphalangia "abnormally short phalanges" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0002764 short tibia " reduced length of the medial and larger bone of the lower leg" [J:12736, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0002896 abnormal bone mineralization "defect in the process by which minerals are deposited into bone" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003055 abnormal epiphyseal plate morphology "malformed or absent cartilagenous center of ossification on the long bones permitting growth of the bone in both directions during development" [MeSH:National Library of Medicine - Medical Subject Headings, 2003]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0003345 decreased number of ribs "fewer than normal numbers of the pairs of bony structures that make up the body wall" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request]
Show

Allelic Composition: Flnbskm2/Flnbskm2
Genetic Background: involves: 129S1/SvImJ * 129X1/SvJ * DBA/2J

 MP:0003408 increased width of hypertrophic chondrocyte zone "increased width of cartilage cell matrix layer " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0003409 decreased width of hypertrophic chondrocyte zone "decreased width of cartilage cell matrix layer " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0003410 abnormal artery development "anomaly in the process of forming the blood vessels that carry blood away from the heart" [J:94740, smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0003419 delayed endochondral bone ossification "late onset of bone formation in bones that form from cartilage" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94631]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0003420 delayed intramembranous bone ossification "late onset of bone formation in bones that form without a cartilagenous intermediate including the cranium and clavicle" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94631]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0003566 abnormal cell adhesion "altered ability of a cell to adhere to another cell or to a non-cellular component of the environment" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0003662 abnormal proliferative zone "germinal layer of the epiphyseal plate where cells are actively dividing as well as producing extracellular matrix" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:96254]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0003961 decreased lean body mass "less than average fat-free physical bulk or volume of the body including all its components except adipose tissue" [honda:Hiraoki Onda, Mouse GEnome Informatics Curator]
Show

Allelic Composition: Fgf9tm1b(KOMP)Wtsi/Fgf9tm1b(KOMP)Wtsi
Genetic Background: C57BL/6N-Fgf9tm1b(KOMP)Wtsi/H

 MP:0004322 abnormal sternebra morphology "any structural anomaly of one segments of the primordial sternum of the embryo; these segments fuse to form the body of the adult vertebrate sternum" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg,Runx2tm1Mjo/Runx2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004355 short radius "reduced length of the short bone of the lateral forearm" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0004441 small occipital bone "reduced size of the bone at the lower, posterior part of the skull" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg,Runx2tm1Mjo/Runx2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004609 vertebral fusion "the union of one or more vertebrae into a single structure" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

Allelic Composition: FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0004620 cervical vertebral fusion "the union of one or more cervical vertebrae into a single structure" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0004623 thoracic vertebral fusion "the union of one or more thoracic vertebrae into a single structure" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbskm2/Flnbskm2
Genetic Background: involves: 129S1/SvImJ * 129X1/SvJ * DBA/2J

 MP:0004624 abnormal thoracic cage "any structural anomaly of the bony and cartilaginous structure enclosing the thoracic cavity, consisting of the thoracic vertebrae, ribs, costal cartilages, and sternum" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbskm2/Flnbskm2
Genetic Background: involves: 129S1/SvImJ * 129X1/SvJ * DBA/2J

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0004674 thin ribs "a more slender appearance of the bones forming the bony wall of the chest" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0004683 absent intervertebral disk "absence of the cartilaginous and gelatinous structure found between vertebrae" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0004686 decreased length of long bones "reduced end-to-end length of the several elongated bones of the extremities" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0004703 abnormal vertebral column "any structural anomaly of the complete structure forming the rostral-caudal axis of the skeleton formed from the alternating segments of vertebra and intervertebral discs which support the spinal cord" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0004950 abnormal brain vasculature "any structural anomaly of the blood vessel network of the brain" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0005108 abnormal ulna morphology "malformation of the medial and larger of the two bones of the forearm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83132]
Show

Allelic Composition: FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0005269 abnormal occipital bone morphology "anomalous structure of the bone at the lower, posterior part of the skull" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0005274 abnormal viscerocranium morphology "anomalous structure or formation of the part of the skull that comprises the facial bones " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0005353 abnormal patella morphology "anomalous structure of the large sesamoid bone that covers the anterior surface of the knee" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:47316]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0005426 tachypnea "rapid breathing" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Flnbskm2/Flnbskm2
Genetic Background: involves: 129S1/SvImJ * 129X1/SvJ * DBA/2J

 MP:0005621 abnormal cell physiology "aberration in the vital processes of the cell " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, hdene:Howard Dene , Mouse Genome Informatics Curator]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0006322 abnormal perichondrium morphology "any structural anomaly of the fibrous connective tissue that surrounds all non-joint end cartilage" [ISBN:0-8036-0655-99 "Taber s Cyclopedic Medical Dictionary, 19th edition", J:117033, MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0006396 decreased long bone epiphyseal plate size "reduced size of the cartilaginous center of ossification on the long bones permitting growth of the bone in both directions during development" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0006429 abnormal hyaline cartilage morphology "any structural anomaly of the bluish-white, glassy, translucent nonvascular, resilient, flexible connective tissue; found primarily in articular cartilage, costal cartilages, the nasal septum, the larynx, and the trachea" [ISBN:0-8036-0655-9 "Taber s Cyclopedic Medical Dictionary", MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0008069 abnormal joint mobility "anomaly in the ability to move joints in a full range of motion and with ease" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0008155 decreased diameter of radius "reduced width of the cross-sectional distance that extends from one lateral edge of the radius, through its center and to the opposite lateral edge" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0008157 decreased diameter of ulna "reduced width of the cross-sectional distance that extends from one lateral edge of the ulna, through its center and to the opposite lateral edge" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0008271 abnormal bone ossification "any anomaly in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance" [GO:0001503]
Show

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 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"]
Show

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0008915 fused carpal bones "anomaly of the nine nodular bones of the joint between the forelimb bones and the front paws/hands resulting in some or all the bones being joined together" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0009780 abnormal chondrocyte physiology "any functional anomaly of nondividing cartilage cells" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0010103 small thoracic cage "reduced size of the bony and cartilaginous structure enclosing the thoracic cavity, consisting of the thoracic vertebrae, ribs, costal cartilages, and sternum" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0010124 decreased bone mineral content "reduction in the amount (usually in grams/cm) of bone mineral divided by a bone-scanned area" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Fgf9tm1b(KOMP)Wtsi/Fgf9tm1b(KOMP)Wtsi
Genetic Background: C57BL/6N-Fgf9tm1b(KOMP)Wtsi/H

 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]
Show

Allelic Composition: FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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]
Show

Allelic Composition: FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0011090 partial perinatal 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 perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0011100 complete preweaning lethality "death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Fgf9tm1b(KOMP)Wtsi/Fgf9tm1b(KOMP)Wtsi
Genetic Background: C57BL/6N-Fgf9tm1b(KOMP)Wtsi/H

 MP:0011108 partial embryonic lethality during organogenesis "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 embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0011110 partial preweaning 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 weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Flnbskm2/Flnbskm2
Genetic Background: involves: 129S1/SvImJ * 129X1/SvJ * DBA/2J

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0011708 decreased fibroblast cell migration "reduced frequency of or less rapid cell migration that is accomplished by extension and retraction of a fibroblast pseudopodium" [MGI:csmith]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0013258 abnormal extracellular matrix morphology "any structural anomaly of the structure lying external to one or more cells, which provides structural support for cells or tissues; in mammals, the extracellular matrix is completely external to the cell " [GO:0031012]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0020040 decreased bone ossification "decrease in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance" [ORCID: orcid.org/0000-0003-4606-0597]
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0020137 decreased bone mineralization "decrease in the rate at which minerals are deposited into bone" []
Show

Allelic Composition: Flnbtm1Vshn/Flnbtm1Vshn
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0020487 abnormal middle cerebral artery morphology "any structural anomaly of the major paired arteries that arise from the internal carotid artery and supply blood to a portion of the frontal lobe and the lateral surface of the temporal and parietal lobes" [http://www.strokecenter.org/professionals/brain-anatomy/blood-vessels-of-the-brain/, https://radiopaedia.org/articles/middle-cerebral-artery]
Show

Allelic Composition: Foxo3tm1.1Rdp/Foxo3tm1.1Rdp,Foxo4tm1.1Rdp/Foxo4tm1.1Rdp
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * FVB/N

 MP:0030029 wide cranial sutures "an abnormally increased width of one or more cranial sutures for age-related norms, generally resulting from delayed suture closure" [HP:0010537]
Show

Allelic Composition: FlnbGt(XD076)Byg/FlnbGt(XD076)Byg,Runx2tm1Mjo/Runx2+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000025234 Arih1 / Q9Z1K5 / E3 ubiquitin-protein ligase ARIH1 / Q9Y4X5* / ariadne RBR E3 ubiquitin protein ligase 1*  / reaction
 ENSMUSG00000035692 Isg15 / Q64339 / Ubiquitin-like protein ISG15 / P05161* / ISG15 ubiquitin-like modifier*  / complex / reaction
 ENSMUSG00000027078 Q9QZU9 / Ube2l6 / ubiquitin-conjugating enzyme E2L 6 / O14933*  / reaction






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2025
contact: otassy@igbmc.fr