ENSMUSG00000041540


Mus musculus

Features
Gene ID: ENSMUSG00000041540
  
Biological name :Sox5
  
Synonyms : P35710 / Sox5 / SRY (sex determining region Y)-box 5
  
Possible biological names infered from orthology : P35711 / SRY-box 5
  
Species: Mus musculus
  
Chr. number: 6
Strand: -1
Band: G3
Gene start: 143828425
Gene end: 144781977
  
Corresponding Affymetrix probe sets: 10549200 (MoGene1.0st)   1423500_a_at (Mouse Genome 430 2.0 Array)   1432189_a_at (Mouse Genome 430 2.0 Array)   1432190_at (Mouse Genome 430 2.0 Array)   1440827_x_at (Mouse Genome 430 2.0 Array)   1452511_at (Mouse Genome 430 2.0 Array)   1455535_at (Mouse Genome 430 2.0 Array)   1459261_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000107377
Ensembl peptide - ENSMUSP00000076403
Ensembl peptide - ENSMUSP00000107378
Ensembl peptide - ENSMUSP00000133041
Ensembl peptide - ENSMUSP00000122786
Ensembl peptide - ENSMUSP00000114602
Ensembl peptide - ENSMUSP00000047567
NCBI entrez gene - 20678     See in Manteia.
MGI - MGI:98367
RefSeq - XM_017321477
RefSeq - XM_006506944
RefSeq - XM_006506945
RefSeq - XM_006506946
RefSeq - XM_011241577
RefSeq - XM_011241578
RefSeq - XM_011241579
RefSeq - XM_011241580
RefSeq - XM_011241581
RefSeq - XM_011241582
RefSeq - XM_017321474
RefSeq - XM_017321475
RefSeq - XM_017321476
RefSeq - NM_001113559
RefSeq - NM_001243163
RefSeq - NM_011444
RefSeq - XM_006506931
RefSeq - XM_006506932
RefSeq - XM_006506933
RefSeq - XM_006506934
RefSeq - XM_006506935
RefSeq - XM_006506936
RefSeq - XM_006506937
RefSeq - XM_006506938
RefSeq - XM_006506939
RefSeq - XM_006506940
RefSeq - XM_006506941
RefSeq - XM_006506942
RefSeq Peptide - NP_001230092
RefSeq Peptide - NP_001334435
RefSeq Peptide - NP_035574
RefSeq Peptide - NP_001107031
swissprot - Q2TBA9
swissprot - Q3TVF9
swissprot - B2KFM4
swissprot - E9PVR0
swissprot - P35710
swissprot - B2KFM9
swissprot - B2KFM8
swissprot - B2KFM7
Ensembl - ENSMUSG00000041540
  

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
 sox5ENSDARG00000011582Danio rerio
 SOX5ENSGALG00000032768Gallus gallus
 SOX5ENSG00000134532Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Sox6 / P40645 / SRY (sex determining region Y)-box 6 / P35712* / SRY-box 6*ENSMUSG0000005191061
Sox13 / Q04891 / Transcription factor SOX-13 / Q9UN79* / SRY-box 13*ENSMUSG0000007064337
Sox30 / Q8CGW4 / Transcription factor SOX-30 / O94993* / SRY-box 30*ENSMUSG0000004048916


Protein motifs (from Interpro)
Interpro ID Name
 IPR009071  High mobility group box domain
 IPR036910  High mobility group box domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001701 in utero embryonic development IMP
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0021953 central nervous system neuron differentiation IGI
 biological_processGO:0032332 positive regulation of chondrocyte differentiation IDA
 biological_processGO:0045165 cell fate commitment IGI
 biological_processGO:0045892 negative regulation of transcription, DNA-templated IDA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IGI
 biological_processGO:0048709 oligodendrocyte differentiation IMP
 biological_processGO:0051216 cartilage development IGI
 biological_processGO:0055059 asymmetric neuroblast division ISO
 biological_processGO:0060164 regulation of timing of neuron differentiation IMP
 biological_processGO:0061036 positive regulation of cartilage development ISO
 biological_processGO:0071560 cellular response to transforming growth factor beta stimulus ISO
 biological_processGO:2000741 positive regulation of mesenchymal stem cell differentiation ISO
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0044798 nuclear transcription factor complex IDA
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding IDA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0003700 DNA-binding transcription factor activity IGI
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0044212 transcription regulatory region DNA binding IDA
 molecular_functionGO:0046982 protein heterodimerization activity IPI


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 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: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 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: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 MP:0000163 abnormal cartilage morphology "anomalous structure or development of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the throax, and tubular structures, but which also comprises most of the skeleton in early fetal life " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 MP:0000164 abnormal cartilage development "anomalous formation of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the throax, and tubular structures, but which also comprises most of the skeleton in early fetal life " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Sox6tm2.2Vlf/Sox6tm2.2Vlf
Genetic Background: involves: 129 * C57BL/6J

 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: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 MP:0000445 short snout "reduced length of the anterior facial part of the muzzle" [J:53370]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

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

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

Allelic Composition: Sox5tm2Vlf/Sox5tm2Vlf,Sox6tm2.1Vlf/Sox6tm2.1Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

 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: Sox5tm2Vlf/Sox5tm2Vlf,Sox6tm2.1Vlf/Sox6tm2.1Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

 MP:0000558 abnormal tibia morphology "atructural anomaly of the medial and larger of the two bones of the lower leg" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Sox5tm2Vlf/Sox5tm2Vlf,Sox6tm2.1Vlf/Sox6tm2.1Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

 MP:0000572 abnormal autopod morphology "malformation of the hand or foot" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Sox5tm2Vlf/Sox5tm2Vlf,Sox6tm2.1Vlf/Sox6tm2.1Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

 MP:0000592 short tail "reduced length of tail compared to control " [J:55583]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 MP:0001258 decreased body length "decreased crown to tail distance compared to controls" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 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: Sox5tm1Vlf/Sox5+,Sox6tm1Vlf/Sox6+
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Sox5tm2Vlf/Sox5tm2Vlf,Sox6tm2.1Vlf/Sox6tm2.1Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

 MP:0001270 distended abdomen "abdomen appears curved outward or swollen; can be due to skeletal axial defects, enlarged visceral organs or megacolon" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 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: Mdm2tm1.1Ypz/Mdm2+,Tg(IghMyc)22Bri/0
Genetic Background: B6.Cg-Mdm2tm1.1Ypz Tg(IghMyc)22Bri

 MP:0001785 edema "an accumulation of an excessive amount of watery fluid in cells or intercellular tissues" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54065]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

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

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

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

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

Allelic Composition: Sox5Tn(sb-lacZ,GFP)IF2.1Jtak/Sox5Tn(sb-lacZ,GFP)IF2.1Jtak
Genetic Background: involves: C3H * C57BL/6 * DBA/2 * ICR

 MP:0002109 abnormal limb morphology "abnormal development of limbs resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Sox5tm2Vlf/Sox5tm2Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

 MP:0002128 abnormal blood circulation "failure or atypical movement in the flow of blood from the heart to the vasculature and back to the heart" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 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: Sox5tm2.1Vlf/Sox5tm2.1Vlf
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J * SJL

Allelic Composition: Sox5tm2Vlf/Sox5tm2Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

Allelic Composition: Sox5tm1.1Tlu/Sox5tm1.1Tlu
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ * FVB/N) or (involves: 129S1/Sv * 129X1/SvJ * CD-1 * FVB/N)

 MP:0002187 abnormal fibula morphology "malformation of the lateral and smaller bone of the lower limb" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Sox5tm2Vlf/Sox5tm2Vlf,Sox6tm2.1Vlf/Sox6tm2.1Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

 MP:0002657 chondrodystrophy "abnormal development of the cartilage primordia of long bones, resulting in abnormally short extremities but normal head and trunk" [il:Ira Lu , Mouse Genome Informatics Curator]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 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: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

Allelic Composition: Sox5tm1Vlf/Sox5+,Sox6tm1Vlf/Sox6+
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0002898 absent cartilage "absence of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the thorax, and tubular structures, but which also comprises most of the skeleton in early fetal life " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 MP:0003048 abnormal cervical vertebrae morphology "malformation of any or all of the seven bony segments of the spine located anterior to the thoracic vertebrae" [MeSH:National Library of Medicine - Medical Subject Headings, 2003, csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Faslpr/Faslpr
Genetic Background: MRL.Cg-Tnfrsf9tm1Byk Faslpr

 MP:0004321 short sternum "reduced length of the long flat bone of the chest which articulates with clavicle and first seven rib pairs" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

Allelic Composition: Sox5tm1Vlf/Sox5+,Sox6tm1Vlf/Sox6+
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Sox5tm2Vlf/Sox5tm2Vlf,Sox6tm2.1Vlf/Sox6tm2.1Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

 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: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 MP:0004672 short ribs "reduced length of the bones forming the bony wall of the chest" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 MP:0004704 short vertebral column "decreased rostral-caudal length 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: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 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: Sox5tm2Vlf/Sox5tm2Vlf,Sox6tm2.1Vlf/Sox6tm2.1Vlf,Tg(Prrx1-cre)1Cjt/?
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL

 MP:0008277 abnormal sternum ossification "anomaly in the process of the formation of the sternum bone by the replacement of cartilage tissue with mineralized bone" [GO:0001958, MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Faslpr/Faslpr
Genetic Background: MRL.Cg-Tnfrsf9tm1Byk Faslpr

 MP:0009886 failure of palatal shelf elevation "the palatal shelves fail to move from a vertical position in the orofacial cavity to a horizontal apposition above the developing tongue" [PMID:16680722]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

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

Allelic Composition: Faslpr/Faslpr
Genetic Background: MRL.Cg-Tnfrsf9tm1Byk Faslpr

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

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

Allelic Composition: Sox5tm2.1Vlf/Sox5tm2.1Vlf
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J * SJL

 MP:0010099 abnormal thoracic cage shape "anomaly in the overall regular dome shape of the ribcage" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

Allelic Composition: Sox5tm2.1Vlf/Sox5tm2.1Vlf
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J * SJL

 MP:0011087 complete neonatal lethality "death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

Allelic Composition: Sox5tm2.1Vlf/Sox5tm2.1Vlf
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J * SJL

Allelic Composition: Sox5Tn(sb-lacZ,GFP)IF2.1Jtak/Sox5Tn(sb-lacZ,GFP)IF2.1Jtak
Genetic Background: involves: C3H * C57BL/6 * DBA/2 * ICR

 MP:0011099 complete lethality throughout fetal growth and development "death of all organisms of a given genotype in a population between the completion of organogenesis and birth (Mus: E14 to approximately E18.5)" [MGI:csmith]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

 MP:0012514 pectus excavatum "a caved-in or sunken appearance of the anterior chest wall; the congenital deformity can either be present at birth or may not be visible until puberty" [MGI:anna]
Show

Allelic Composition: Cdkn2atm1Rdp/Cdkn2atm1Rdp,Tg(Mt1-HGFSF)19Lmb/0
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N * SJL

  


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






 

0 s.

 
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