ENSMUSG00000021136


Mus musculus

Features
Gene ID: ENSMUSG00000021136
  
Biological name :Smoc1
  
Synonyms : Smoc1 / SPARC related modular calcium binding 1
  
Possible biological names infered from orthology : Q9H4F8
  
Species: Mus musculus
  
Chr. number: 12
Strand: 1
Band: D1
Gene start: 81026808
Gene end: 81186414
  
Corresponding Affymetrix probe sets: 10396936 (MoGene1.0st)   1448321_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000021564
Ensembl peptide - ENSMUSP00000122858
Ensembl peptide - ENSMUSP00000105976
NCBI entrez gene - 64075     See in Manteia.
MGI - MGI:1929878
RefSeq - XM_006516135
RefSeq - NM_001146217
RefSeq - NM_022316
RefSeq Peptide - NP_071711
RefSeq Peptide - NP_001139689
swissprot - E9QKW2
swissprot - A0A0R4J1E4
swissprot - D3Z3A3
Ensembl - ENSMUSG00000021136
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 smoc1ENSDARG00000088255Danio rerio
 SMOC1ENSGALG00000009415Gallus gallus
 SMOC1ENSG00000198732Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Smoc2 / Q8CD91 / SPARC related modular calcium binding 2 / Q9H3U7*ENSMUSG0000002388649


Protein motifs (from Interpro)
Interpro ID Name
 IPR000716  Thyroglobulin type-1
 IPR002350  Kazal domain
 IPR011992  EF-hand domain pair
 IPR018247  EF-Hand 1, calcium-binding site
 IPR019577  SPARC/Testican, calcium-binding domain
 IPR036058  Kazal domain superfamily
 IPR036857  Thyroglobulin type-1 superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001654 eye development IEA
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0045667 regulation of osteoblast differentiation IEA
 biological_processGO:0060173 limb development IEA
 molecular_functionGO:0005509 calcium ion binding IEA
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0050840 extracellular matrix binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000111 cleft palate "congenital fissure of the tissues normally uniting to form the palate" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

 MP:0000433 microcephaly "an abnormally small head" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Slc6a3tm1b(KOMP)Wtsi/Slc6a3+
Genetic Background: C57BL/6N-Slc6a3tm1b(KOMP)Wtsi/J

 MP:0000438 abnormal skull morphology "anomalous structure or development of the cranium" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Slc6a3tm1b(KOMP)Wtsi/Slc6a3+
Genetic Background: C57BL/6N-Slc6a3tm1b(KOMP)Wtsi/J

 MP:0000443 abnormal snout morphology "anomalous structure or development of the anterior facial part of the muzzle" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Slc6a3tm1b(KOMP)Wtsi/Slc6a3+
Genetic Background: C57BL/6N-Slc6a3tm1b(KOMP)Wtsi/J

 MP:0000455 abnormal maxilla morphology "malformation of the upper bony framework of the mouth where the superior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Slc6a3tm1b(KOMP)Wtsi/Slc6a3+
Genetic Background: C57BL/6N-Slc6a3tm1b(KOMP)Wtsi/J

 MP:0000556 abnormal hindlimb morphology "malformation of the entire posterior extremities" [MGI:tc]
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Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0000564 syndactyly "any degree of webbing or fusion of the digits, may involve only soft tissues or also can include bone" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

Allelic Composition: Smoc1Tn(sb-lacZ,GFP)IR3.1Jtak/Smoc1Tn(sb-lacZ,GFP)IR3.1Jtak
Genetic Background: involves: C3H * C57BL/6 * DBA/2 * ICR

Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

Allelic Composition: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

 MP:0000565 oligodactyly "congenital condition in which some digits or parts of digits are missing" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:53370]
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Allelic Composition: Slc6a3tm1b(KOMP)Wtsi/Slc6a3+
Genetic Background: C57BL/6N-Slc6a3tm1b(KOMP)Wtsi/J

 MP:0000566 synostosis "osseous union of two bones that are not normally connected" [J:13049]
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Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0000571 interdigital webbing "fold of skin, or web, between the toes that is not normally present" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
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Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0000572 abnormal autopod morphology "malformation of the hand or foot" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0000576 clubbed feet "congenital deformation of the feet; foot is plantarflexed, inverted and adducted" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61295]
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Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

Allelic Composition: Smoc1Tn(sb-lacZ,GFP)IR3.1Jtak/Smoc1Tn(sb-lacZ,GFP)IR3.1Jtak
Genetic Background: involves: C3H * C57BL/6 * DBA/2 * ICR

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

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1+
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi/H

 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: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

 MP:0001297 microphthalmia "reduced average size of the eyes" [J:18048]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0001325 abnormal retina morphology "structural or developmental anomaly of the thin layer of neural tissue lining the back of the eyeball which contains visual receptors " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

Allelic Composition: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

 MP:0001326 retinal degeneration "pathological change in the thin layer of neural tissue lining the back of the eyeball, which contains visual receptors and can result in the impairment or cessation of retinal neural function" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, NMF:Stephanie Pretel, Neuroscience Mutagenesis Facility Curator]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0001333 absent optic nerve "absence of the second cranial nerve which is responsible for conveying visual information from the retina to the brain" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

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

Allelic Composition: Slc6a3tm1b(KOMP)Wtsi/Slc6a3+
Genetic Background: C57BL/6N-Slc6a3tm1b(KOMP)Wtsi/J

 MP:0001698 reduced embryo size "smaller proportions of embryo compared to littermates" [J:61790]
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Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

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

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0002075 abnormal coat color "irregular or unusual pigmentation pattern of the hair in relation to control animals" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Slc38a10tm2a(EUCOMM)Wtsi/Slc38a10tm2a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Slc38a10tm2a(EUCOMM)Wtsi/H

 MP:0002110 abnormal digit morphology "abnormal development of the digits resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Slc6a3tm1b(KOMP)Wtsi/Slc6a3+
Genetic Background: C57BL/6N-Slc6a3tm1b(KOMP)Wtsi/J

 MP:0002546 mydriasis "dilation of one or both pupils" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Slc6a3tm1b(KOMP)Wtsi/Slc6a3+
Genetic Background: C57BL/6N-Slc6a3tm1b(KOMP)Wtsi/J

 MP:0002765 short fibula "reduced length of the lateral and smaller of bone of the lower leg" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:12736]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0002792 abnormal retinal vascularization "malformation or disorganization of the blood vessels supplying the retina" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
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Allelic Composition: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

 MP:0002875 decreased erythrocyte count "reduced number of the cells in the blood that carry oxygen, red blood cells, per unit" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Scribtm1b(NCOM)Mfgc/Scribtm1b(NCOM)Mfgc
Genetic Background: C57BL/6N-Scribtm1a(NCOM)Mfgc/Tcp

 MP:0002932 abnormal joint "defect in the articulation point of two or more bones" [RGD:Rat Genome Database submission, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 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: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

 MP:0003757 high palate "greater distance upward to the roof of the oral cavity than usual" [ncbi:Matthew Mailman, NCBI request]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0004358 bowed tibia "increased curvature of the medial and larger of the two bones of the lower leg" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0004509 abnormal pelvic girdle bone morphology "any structural anomaly of the bones of the pelvis by which the limbs attach to the axial skeleton " [MGI:cwg "Carroll-Ann W. Goldsmith, Mouse Genome Informatics Curator"]
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Allelic Composition: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

 MP:0004642 fused metatarsal bones "improper union of the five bones of the hindpaws/feet that articulate proximally with the cuneiform and cuboid bones of the tarsus and distally with the phalanges" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0004924 abnormal behavior "anomalies in the actions, reactions, or performance of an organism in response to external or internal stimuli compared to controls" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Scribtm1b(NCOM)Mfgc/Scribtm1b(NCOM)Mfgc
Genetic Background: C57BL/6N-Scribtm1a(NCOM)Mfgc/Tcp

 MP:0005201 abnormal retinal pigment epithelium morphology "anomaly in the epithelial layer of the retina composed of cells containing pigment granules " [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

 MP:0005287 narrow eye opening "less than the normal distance from one eyelid to the other " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, J:71350]
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Allelic Composition: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

 MP:0005430 absent fibula "missing the lateral and shorter of the two bones of the lower leg" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:86196]
Show

Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

 MP:0006221 optic nerve hypoplasia "less than the normal number of fibers in the optic nerve" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

 MP:0006243 abnormal pupil dilation reaction to light "the pupil fails to constrict fully when exposed to bright light" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

 MP:0006309 decreased retinal ganglion cell number "reduced number of ganglion neurons located in the innermost nuclear layer of the retina of that receive visual information from photoreceptors via various intermediate cells such as bipolar cells, amacrine cells, and horizontal cells; axons from these cells form the optic nerve and connect mainly to the lateral geniculate nucleus (LGN) and to the suprachiasmatic nucleus in the brain" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0008259 abnormal optic disc morphology "any structural anomaly of the area in the retina where all of the axons of the ganglion cells exit the retina to form the optic nerve" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

 MP:0009874 abnormal interdigital cell death "change in the expected number of cells undergoing programmed cell death (apoptosis) in the autopod during development, precluding the sculpting of normal digits" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0010097 abnormal retinal blood vessel morphology "any structural anomaly of the blood vessels supplying the retina" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

 MP:0010714 coloboma of the iris "congenital defect of the iris in which some part of the structure is absent" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

 MP:0010715 coloboma of the retina "congenital defect of the retina in which some part of the structure is absent" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

 MP:0010772 abnormal pollex morphology "any structural anomaly of the first or primary digit on the radial side of the hand" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL

 MP:0011085 complete postnatal lethality "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
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Allelic Composition: Ptentm1Hwu/Ptentm1Hwu,Tg(Vil1-cre)997Gum/0
Genetic Background: involves: 129S4/SvJae * BALB/c * 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]
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Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi

 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]
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Allelic Composition: Smoc1tm1b(EUCOMM)Wtsi/Smoc1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smoc1tm1b(EUCOMM)Wtsi/H

  


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






 

0 s.

 
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