ENSMUSG00000074622


Mus musculus

Features
Gene ID: ENSMUSG00000074622
  
Biological name :Mafb
  
Synonyms : Mafb / P54841 / Transcription factor MafB
  
Possible biological names infered from orthology : MAF bZIP transcription factor B / Q9Y5Q3
  
Species: Mus musculus
  
Chr. number: 2
Strand: -1
Band: H2
Gene start: 160363703
Gene end: 160367065
  
Corresponding Affymetrix probe sets: 10489246 (MoGene1.0st)   1451715_at (Mouse Genome 430 2.0 Array)   1451716_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000096728
NCBI entrez gene - 16658     See in Manteia.
MGI - MGI:104555
RefSeq - NM_010658
RefSeq Peptide - NP_034788
swissprot - P54841
Ensembl - ENSMUSG00000074622
  

This gene has been taged as a transcription factor by TFT
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 mafbaENSDARG00000017121Danio rerio
 mafbbENSDARG00000070542Danio rerio
 MAFBENSGALG00000003670Gallus gallus
 MAFBENSG00000204103Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Maf / P54843 / Transcription factor Maf / O75444* / MAF bZIP transcription factor*ENSMUSG0000005543559
Mafa / Q8CF90 / Transcription factor MafA / Q8NHW3* / MAF bZIP transcription factor A*ENSMUSG0000004759157
Nrl / P54846 / Neural retina-specific leucine zipper protein / P54845* / neural retina leucine zipper*ENSMUSG0000004063238
Mafk / Q61827 / v-maf musculoaponeurotic fibrosarcoma oncogene family, protein K (avian) / O60675* / MAF bZIP transcription factor K*ENSMUSG0000001814323
Mafg / O54790 / Transcription factor MafG / O15525* / MAF bZIP transcription factor G*ENSMUSG0000005151020
Maff / O54791 / Transcription factor MafF / Q9ULX9* / MAF bZIP transcription factor F*ENSMUSG0000004262220


Protein motifs (from Interpro)
Interpro ID Name
 IPR004826  Basic leucine zipper domain, Maf-type
 IPR004827  Basic-leucine zipper domain
 IPR008917  Transcription factor, Skn-1-like, DNA-binding domain superfamily
 IPR013592  Maf transcription factor, N-terminal
 IPR024874  Transcription factor Maf family
 IPR028571  Transcription factor MafB


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated ISO
 biological_processGO:0006357 regulation of transcription by RNA polymerase II IDA
 biological_processGO:0006366 transcription by RNA polymerase II IEA
 biological_processGO:0007379 segment specification IMP
 biological_processGO:0007585 respiratory gaseous exchange IMP
 biological_processGO:0021571 rhombomere 5 development IMP
 biological_processGO:0021572 rhombomere 6 development IMP
 biological_processGO:0021599 abducens nerve formation IMP
 biological_processGO:0033077 T cell differentiation in thymus IMP
 biological_processGO:0035284 brain segmentation IMP
 biological_processGO:0042472 inner ear morphogenesis IMP
 biological_processGO:0045647 negative regulation of erythrocyte differentiation IEA
 biological_processGO:0045671 negative regulation of osteoclast differentiation IDA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IEA
 biological_processGO:0048538 thymus development IMP
 cellular_componentGO:0005634 nucleus IDA
 cellular_componentGO:0005654 nucleoplasm TAS
 cellular_componentGO:0005667 transcription factor complex IDA
 molecular_functionGO:0000978 RNA polymerase II proximal promoter sequence-specific DNA binding IMP
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding IEA
 molecular_functionGO:0001077 transcriptional activator activity, RNA polymerase II proximal promoter sequence-specific DNA binding IMP
 molecular_functionGO:0003677 DNA binding IDA
 molecular_functionGO:0003700 DNA-binding transcription factor activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008134 transcription factor binding IEA
 molecular_functionGO:0042803 protein homodimerization activity IEA
 molecular_functionGO:0046982 protein heterodimerization activity IEA
 molecular_functionGO:1990837 sequence-specific double-stranded DNA binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000026 abnormal inner ear morphology "malformation or malfunction of any components of the labyrinth, including the semicircular canals, vestibule and cochlea" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0000035 abnormal membranous labyrinth "malformations in the complex arrangement of communicating canaliculi and sacs suspended within the cavity of the bony labyrinth of the inner ear" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23837]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0000041 absent endolymphatic duct "missing small membranous canal of the inner ear; connecting membranous labyrinth with the endolymphatic sac" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
Show

Allelic Composition: Usp18ity9/Usp18tm1Dez
Genetic Background: involves: 129 * C57BL/6 * FVB/N

 MP:0000522 cysts in kidney cortex "abnormal membranous sacs appearing in the renal lobules, tubules and glomeruli" [J:50844]
Show

Allelic Composition: S1pr2tm1Ajml/S1pr2tm1Ajml
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0000527 abnormal kidney development "anomalous differentiation of the paired organs responsible for urine secretion" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Apptm1Ck/Apptm1Ck,Psen1tm1Mpm/Psen1tm1Mpm,Tg(MAPT)8cPdav/0
Genetic Background: B6.Cg-Psen1tm1Mpm Apptm1Ck Tg(MAPT)8cPdav

 MP:0000533 kidney hemorrhage "bleeding in the organ of excretion" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator]
Show

Allelic Composition: S1pr2tm1Ajml/S1pr2tm1Ajml
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0000933 abnormal rhombomere morphology "malformation of the transverse segments in the hindbrain region of the developing neural tube" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
Show

Allelic Composition: Recktm1Ito/Recktm1Ito
Genetic Background: involves: 129P2/OlaHsd

 MP:0001394 circling "repeated, compulsive movement in a circle; often associated with inner ear defects" [MGI:CLS, J:61295]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0001399 hyperactivity "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 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: CoblC101/CoblC101,Vangl2Lp/Vangl2+
Genetic Background: involves: 129S2/SvPas * LPT/LeJ

Allelic Composition: Mafbtm1.2Good/Mafbtm1.2Good
Genetic Background: involves: 129S4/SvJae * C57BL/6 * SJL

 MP:0001922 reduced male fertility "reduced ability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61340]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0001923 reduced female fertility "reduced ability of female to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0001943 abnormal respiration "anomaly in the movement of gases into and out of the lung " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: CoblC101/CoblC101,Vangl2Lp/Vangl2+
Genetic Background: involves: 129S2/SvPas * LPT/LeJ

 MP:0001951 abnormal breathing "irregular or atypical breathing pattern " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:17489]
Show

Allelic Composition: CoblC101/CoblC101,Vangl2Lp/Vangl2+
Genetic Background: involves: 129S2/SvPas * LPT/LeJ

 MP:0001953 respiratory failure "cessation of or failure to commence breathing" [MGI:cls, J:60159]
Show

Allelic Composition: CoblC101/CoblC101,Vangl2Lp/Vangl2+
Genetic Background: involves: 129S2/SvPas * LPT/LeJ

 MP:0001954 respiratory distress "physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931]
Show

Allelic Composition: CoblC101/CoblC101,Vangl2Lp/Vangl2+
Genetic Background: involves: 129S2/SvPas * LPT/LeJ

Allelic Composition: Mafbtm1.2Good/Mafbtm1.2Good
Genetic Background: involves: 129S4/SvJae * C57BL/6 * SJL

 MP:0001957 apnea "absence of breathing; sometimes episodic" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17384]
Show

Allelic Composition: CoblC101/CoblC101,Vangl2Lp/Vangl2+
Genetic Background: involves: 129S2/SvPas * LPT/LeJ

Allelic Composition: Mafbtm1.1Good/Mafbtm1Jeng,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * SJL

 MP:0002135 abnormal kidney morphology "abnormal development of the kidney resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: S1pr2tm1Ajml/S1pr2tm1Ajml
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

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

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Apptm1Ck/Apptm1Ck,Psen1tm1Mpm/Psen1tm1Mpm,Tg(MAPT)8cPdav/0
Genetic Background: B6.Cg-Psen1tm1Mpm Apptm1Ck Tg(MAPT)8cPdav

 MP:0002428 abnormal semicircular canal "anomaly of the organ of balance composed of three long bony tubes of the labyrinth" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Usp18ity9/Usp18tm1Dez
Genetic Background: involves: 129 * C57BL/6 * FVB/N

 MP:0002703 abnormal renal tubules "anomalous structure or development of the loops of Henle and collecting ducts in the kidney" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: S1pr2tm1Ajml/S1pr2tm1Ajml
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0002855 abnormal cochlear ganglion morphology "malformation, malfunction or absence of the group of nerve cell bodies that conveys auditory sensation from the organ of Corti to the hindbrain and resides on the cochlear part of the vestibulocochlear nerve (eighth cranial nerve)" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Mafbtm1.1Good/Mafbtm1Jeng,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * SJL

 MP:0003077 abnormal cell cycle "failure to progress or abnormal progression through the stages of of the cell cycle" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:91266]
Show

Allelic Composition: Usp18ity9/Usp18tm1Dez
Genetic Background: involves: 129 * C57BL/6 * FVB/N

 MP:0003308 abnormal cochlear sensory epithelium 
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0003624 anuria "inability to form or excrete urine" [ncbi:Matthew Mailman, NCBI request]
Show

Allelic Composition: S1pr2tm1Ajml/S1pr2tm1Ajml
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0003633 abnormal nervous system physiology 
Show

Allelic Composition: CoblC101/CoblC101,Vangl2Lp/Vangl2+
Genetic Background: involves: 129S2/SvPas * LPT/LeJ

 MP:0004045 abnormal cell cycle checkpoint function "anomaly in the amount of time spent at the points in the cell cycle (end of G1 phase, end of G2 phase, and during metaphase) which prevent the cell from progressing to the next phase when conditions are unfavorable" [smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Mafbkr/Mafbkr
Genetic Background: CBA.Cg-Mafbkr

 MP:0004153 increased renal tubule apoptosis "increase in the number of renal tubule cells undergoing programmed cell death" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: S1pr2tm1Ajml/S1pr2tm1Ajml
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0004289 abnormal bony labyrinth "any structural abnormality in the series of cavities (cochlea, vestibule, and semicircular canals) contained within the otic capsule of the petrous portion of the temporal bone; the bony labyrinth is filled with perilymph, in which the delicate, endolymph-filled membranous labyrinth is suspended" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0004505 decreased renal glomerulus number "reduced number of the capillary loops of the kidney that normally function as a filtration unit" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Mafbtm1Jeng/Mafbtm1Jeng
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0004562 abnormal inner hair cell synaptic ribbon morphology "any structural abnormality in the presynaptic active zone of mature cochlear IHCs which usually contain a single synaptic ribbon, i.e. a submicrometer, electron-dense structure tethering synaptic vesicles; each spiral ganglion neuron receives input from only one IHC synapse" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Mafbtm1.1Good/Mafbtm1Jeng,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * SJL

 MP:0005277 abnormal brainstem morphology "anomalous structure of the midbrain, pons, or medulla" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:82670]
Show

Allelic Composition: CoblC101/CoblC101,Vangl2Lp/Vangl2+
Genetic Background: involves: 129S2/SvPas * LPT/LeJ

 MP:0005307 head tossing "compulsive flailing of the head in multiple directions" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0005553 increased circulating creatinine level "greater than the normal blood concentration of this product of creatine catabolism; abnormal levels indicative of renal dysfunction" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, RGD:Rat Genome Database submission]
Show

Allelic Composition: S1pr2tm1Ajml/S1pr2tm1Ajml
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0006011 abnormal endolymphatic duct morphology "any structural alteration in the small membranous canal, connecting with both saccule and utricle of the membranous labyrinth, passing through the aqueduct of vestibule, and terminating in the endolymphatic sac." [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Usp18ity9/Usp18tm1Dez
Genetic Background: involves: 129 * C57BL/6 * FVB/N

 MP:0006030 abnormal otic vesicle formation "anomalous formation of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:57313:]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: Mafbkr/Mafbkr
Genetic Background: CBA.Cg-Mafbkr

 MP:0006108 abnormal hindbrain development "anomaly in the formation or pattering of the caudal region of the brain" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:93573]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0006287 inner ear cysts "abnormal membranous sacs in any component of the labyrinth, including the semicircular canals, vestibule and cochlea" [J:111415, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: Mafbtm1Jeng/Mafbtm1Jeng
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Mafbkr/Mafbkr
Genetic Background: CBA.Cg-Mafbkr

Allelic Composition: Mafbtm1.2Good/Mafbtm1.2Good
Genetic Background: involves: 129S4/SvJae * C57BL/6 * SJL

 MP:0008139 fused podocyte foot processes "coalescence of the footlike extension of podocytes that interdigitate with one another to form the walls of the glomerular capillaries " [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Mafbtm1Jeng/Mafbtm1Jeng
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0009913 abnormal hyoid bone greater horn morphology "any structural anomaly of the larger and more lateral of the paired processes on either side of the hyoid bone" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Recktm1Ito/Recktm1Ito
Genetic Background: involves: 129P2/OlaHsd

 MP:0010395 abnormal branchial arch development "abnormal formation of the of the transient structures of the embryo that develop into regions of the head, neck and ears" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Recktm1Ito/Recktm1Ito
Genetic Background: involves: 129P2/OlaHsd

 MP:0010396 ectopic branchial arch "abnormal location of any of the transient structures of the embryo resulting in misplaced regions of the head, neck and/or ears" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Recktm1Ito/Recktm1Ito
Genetic Background: involves: 129P2/OlaHsd

 MP:0010397 abnormal otic capsule development "any anomaly in the embryonic cartilage covering that surrounds the inner ear mechanism and develops into bone" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 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]
Show

Allelic Composition: Mafbtm1Jeng/Mafbtm1Jeng
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Mafbtm1.2Good/Mafbtm1.2Good
Genetic Background: involves: 129S4/SvJae * C57BL/6 * SJL

Allelic Composition: Mafbtm1.1Good/Mafbtm1Jeng,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * SJL

 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: CoblC101/CoblC101,Vangl2Lp/Vangl2+
Genetic Background: involves: 129S2/SvPas * LPT/LeJ

 MP:0011932 abnormal endocrine pancreas development 
Show

Allelic Composition: X/SryAKR/J,Tht/Tht+
Genetic Background: involves: AKR/J * C57BL/6J

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
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Allelic Composition: Mafbtm1.1Good/Mafbtm1Jeng,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * SJL

 MP:0012796 abnormal rhombomere 4 morphology "any structural anomaly of the fourth transiently divided segment of the developing rhombencephalon; rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates; rhombomeres are numbered in caudal to rostral order" [MGI:anna, MGI:csmith, UBERON:0005511]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0012800 abnormal rhombomere 5 morphology "any structural anomaly of the fifth transiently divided segment of the developing rhombencephalon; rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates; rhombomeres are numbered in caudal to rostral order" [MGI:anna, MGI:csmith, UBERON:0005515]
Show

Allelic Composition: Dlx5tm1Jlr/Dlx5+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0014167 ectopic bone "the appearance of an extra bone structure at an atypical location" [MGI:csmith]
Show

Allelic Composition: Recktm1Ito/Recktm1Ito
Genetic Background: involves: 129P2/OlaHsd

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000052684 Jun / P05627 / jun proto-oncogene / P05412* / Jun proto-oncogene, AP-1 transcription factor subunit*  / complex






 

1 s.

 
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