ENSMUSG00000028173


Mus musculus

Features
Gene ID: ENSMUSG00000028173
  
Biological name :Wls
  
Synonyms : Q6DID7 / Wls / wntless WNT ligand secretion mediator
  
Possible biological names infered from orthology : Q5T9L3
  
Species: Mus musculus
  
Chr. number: 3
Strand: 1
Band: H4
Gene start: 159839672
Gene end: 159938664
  
Corresponding Affymetrix probe sets: 10497149 (MoGene1.0st)   1423824_at (Mouse Genome 430 2.0 Array)   1423825_at (Mouse Genome 430 2.0 Array)   1437434_a_at (Mouse Genome 430 2.0 Array)   1458319_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000067898
Ensembl peptide - ENSMUSP00000142774
Ensembl peptide - ENSMUSP00000143475
NCBI entrez gene - 68151     See in Manteia.
MGI - MGI:1915401
RefSeq - XM_006501964
RefSeq - NM_001356350
RefSeq - NM_026582
RefSeq Peptide - NP_001343279
RefSeq Peptide - NP_080858
swissprot - Q6DID7
swissprot - A0A0G2JEH4
Ensembl - ENSMUSG00000028173
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 wlsENSDARG00000009534Danio rerio
 WLSENSGALG00000011238Gallus gallus
 WLSENSG00000116729Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR009551  Protein wntless


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001707 mesoderm formation IMP
 biological_processGO:0006886 intracellular protein transport ISO
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0009948 anterior/posterior axis specification IMP
 biological_processGO:0016055 Wnt signaling pathway IMP
 biological_processGO:0030177 positive regulation of Wnt signaling pathway ISS
 biological_processGO:0030901 midbrain development IMP
 biological_processGO:0030902 hindbrain development IMP
 biological_processGO:0031017 exocrine pancreas development IMP
 biological_processGO:0061355 Wnt protein secretion ISO
 biological_processGO:0061357 positive regulation of Wnt protein secretion ISS
 biological_processGO:0090263 positive regulation of canonical Wnt signaling pathway IMP
 cellular_componentGO:0000139 Golgi membrane ISO
 cellular_componentGO:0005768 endosome IEA
 cellular_componentGO:0005769 early endosome ISO
 cellular_componentGO:0005783 endoplasmic reticulum IEA
 cellular_componentGO:0005789 endoplasmic reticulum membrane ISO
 cellular_componentGO:0005794 Golgi apparatus ISO
 cellular_componentGO:0005802 trans-Golgi network ISO
 cellular_componentGO:0005886 plasma membrane ISO
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0030659 cytoplasmic vesicle membrane IEA
 cellular_componentGO:0031410 cytoplasmic vesicle ISO
 cellular_componentGO:0031901 early endosome membrane IEA
 cellular_componentGO:0032590 dendrite membrane IEA
 cellular_componentGO:0032839 dendrite cytoplasm IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0017147 Wnt-protein binding ISO
 molecular_functionGO:0031852 mu-type opioid receptor binding IEA


Pathways (from Reactome)
Pathway description
WNT ligand biogenesis and trafficking


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000060 delayed bone ossification "late onset of the formation of bone" [J:40203]
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Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0000074 abnormal neurocranium morphology "malformed bones of the skull enclosing the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:55583]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 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]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0000219 increased neutrophil count "greater than normal neutrophil numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000324 increased mast cell number "greater than expected number of the granulated cells found in most tissues and which contain large amounts of histamine and heparin in granules" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Ctnnb1tm2Kem/Ctnnb1tm2Kem,Tg(Krt1-15-cre/PGR)22Cot/0
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL

Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000352 decreased cell proliferation "less than the normal growth and reproduction of similar cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0000377 abnormal hair follicle "malformed invagination of the epidermis from which the hair shaft develops" [J:65031]
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Allelic Composition: Ctnnb1tm2Kem/Ctnnb1tm2Kem,Tg(Krt1-15-cre/PGR)22Cot/0
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL

 MP:0000379 reduced hair follicle number "fewer number of the epidermal invaginations from which the hair shaft develops" [J:15108]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000416 sparse fur "fur that is significantly less dense" [J:46854]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Tg(Foxn1-cre)1Tbo/0
Genetic Background: involves: C57BL/6

 MP:0000428 abnormal craniofacial morphology "anomalous structure or development of the face and/or cranium" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Wlstm1.2Whsu/Wlstm1.2Whsu
Genetic Background: involves: 129S6/SvEvTac

 MP:0000547 short limbs "reduced average length of the extremities" [MGI:CLS, J:61509]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0000550 abnormal forelimb morphology "malformation of the entire anterior extremities" [MGI:tc]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0000556 abnormal hindlimb morphology "malformation of the entire posterior extremities" [MGI:tc]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 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: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 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: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0000613 abnormal salivary gland morphology "malformed saliva-secreting glands of the oral cavity" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:63764]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0000733 abnormal muscle development "anomalous differentiation of muscle tissue" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0000847 abnormal metencephalon morphology "any malformation or absence of the anterior part of the rhombencephalon" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA/J * SJL

 MP:0000850 absent cerebellum "missing the part of the metencephalon that lies in the posterior cranial fossa dorsal to the pons and medulla that is concerned with the coordination of movement" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:19212, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA/J * SJL

Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0001056 abnormal cranial nerve morphology "any anomaly, deformity, or malformation of any of the twelve nerves that emerge from the cranium as opposed to the spinal nerves" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:45302]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0001190 reddish skin "skin has a more intense ruddy appearance than normal, often due to capillary congestion" [J:65038]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001192 scaly skin "skin covered with shedding scales or flakes" [J:65146]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001195 flaky skin "shedding scales on the skin " [J:56641]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001199 thin skin "reduced thickness of the outer protective layer of the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49471]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001216 abnormal epidermal layer morphology "anomalous structure or development of the superficial epithelial portion of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ctnnb1tm2Kem/Ctnnb1tm2Kem,Tg(Krt1-15-cre/PGR)22Cot/0
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL

 MP:0001243 abnormal dermal layer morphology "malformed or atypical condition of the dermal layer of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:56777]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0001244 thin dermal layer "reduced thickness of the dermis" [J:65030]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
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]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001428 adipsia "absence of thirst or lack of desire to drink " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:30404]
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Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0001674 abnormal triploblastic development "abnormal development of the three primary germ layers" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator]
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Allelic Composition: Hsd11b1tm1.1Ggla/Hsd11b1tm1.1Ggla
Genetic Background: involves: 129P2/OlaHsd

 MP:0001675 abnormal ectoderm development "failure or abnormality in the formation of the ectoderm during gastrulation" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Hsd11b1tm1.1Ggla/Hsd11b1tm1.1Ggla
Genetic Background: involves: 129P2/OlaHsd

 MP:0001676 abnormal apical ectodermal ridge "malformation of the multilayered ectodermal region at the tip of a limb bud necessary for the proper development of the underlying mesenchyme" [MGI:tc]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0001679 thin apical ectodermal ridge "decrease in the thickness of the multilayered ectodermal region at the tip of a limb bud necessary for the proper development of the underlying mesenchyme" [MGI:tc]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0001683 absent mesoderm "missing or failure to differentiate the middle primary germ layer " [J:40594]
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Allelic Composition: Hsd11b1tm1.1Ggla/Hsd11b1tm1.1Ggla
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Wlstm1.2Whsu/Wlstm1.2Whsu
Genetic Background: involves: 129S6/SvEvTac

 MP:0001685 abnormal endoderm development "failure or abnormality in the formation of the endoderm during gastrulation" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Hsd11b1tm1.1Ggla/Hsd11b1tm1.1Ggla
Genetic Background: involves: 129P2/OlaHsd

 MP:0001693 failure of primitive streak formation "inability to form the epiblast ridge from which arises the germ layers of the embryo" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:33880]
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Allelic Composition: Hsd11b1tm1.1Ggla/Hsd11b1tm1.1Ggla
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,Tg(EIIa-cre)C5379Lmgd/0
Genetic Background: involves: 129S/SvEv * FVB/N * SJL

Allelic Composition: Wlstm1.2Whsu/Wlstm1.2Whsu
Genetic Background: involves: 129S6/SvEvTac

 MP:0001730 embryonic growth arrest "the cessation of development beyond a particular stage" [J:17509]
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Allelic Composition: KitlSl-10H/Kitl+
Genetic Background: involves: 101/H * C3H/HeH

Allelic Composition: Wlstm1.2Whsu/Wlstm1.2Whsu
Genetic Background: involves: 129S6/SvEvTac

 MP:0001732 postnatal growth retardation "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001823 thymus hypoplasia "small size due to reduced cell number in the thymus" [J:23255]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0002073 abnormal hair growth "absence or reduced amount of hair or abnormal onset of hair growth cycle or development" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Prdm4tm1b(EUCOMM)Liz/Prdm4tm1b(EUCOMM)Liz
Genetic Background: involves: 129S/SvEv * C57BL/6 * CBA

 MP:0002081 perinatal lethality "death anytime between E18.5 and postnatal day 1 " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,Tg(EIIa-cre)C5379Lmgd/0
Genetic Background: involves: 129S/SvEv * FVB/N * SJL

 MP:0002083 premature death "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0002084 abnormal developmental patterning "abnormal systematic arrangement of the developing body along an axis" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Hsd11b1tm1.1Ggla/Hsd11b1tm1.1Ggla
Genetic Background: involves: 129P2/OlaHsd

 MP:0002092 abnormal eye morphology "abnormal development of the eye tissues resulting in morphological abnormality or abnormal structure of the visual system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0002100 abnormal tooth morphology "atypical size, shape or hard tissue structure of the teeth " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0002102 abnormal ear morphology "structural or developmental anomaly of any of the structures involved in the ear or vestibular system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Prdm4tm1b(EUCOMM)Liz/Prdm4tm1b(EUCOMM)Liz
Genetic Background: involves: 129S/SvEv * C57BL/6 * CBA

 MP:0002145 abnormal T lymphocyte development "atypical production of or inability to produce mature T cells, and/or accumulation of T cell precursors" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * 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]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA/J * SJL

 MP:0002152 abnormal brain morphology "anomalous structure of or abnormal development of the brain, one of the two components of the central nervous system and the center of thought and emotion; controls coordination, bodily activities and the interpretation of information from the senses (sight, hearing, smell, etc.)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, http://cancerweb.ncl.ac.uk]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0002233 abnormal nose morphology "any structural anomaly of the organ that is specialized for smell and is part of the respiratory system " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0002444 abnormal T cell physiology "anomalous response of T lymphocytes" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0002655 abnormal keratinocyte morphology "structural or developmental anomaly of the cells of the epidermis that produce keratin in the process of differentiating into the dead and fully keratinized cells of the stratum corneum" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ctnnb1tm2Kem/Ctnnb1tm2Kem,Tg(Krt1-15-cre/PGR)22Cot/0
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * 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]
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Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 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]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 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]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0002796 impaired skin barrier function "impaired ability of the skin to regulate water loss; frequently leads to dehydration" [J:56641]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003413 hair follicle degeneration "a retrogressive impairment of function or destruction of the hair follicle" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator, J:94517]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003644 thymus atrophy "wasting of the thymus resulting in reduced size " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003704 abnormal hair follicle development "anomalous development of the epidermis from which the hair shaft develops " [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0003854 abnormal forelimb stylopod morphology 
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0003857 abnormal hindlimb zeugopod morphology 
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0003864 abnormal midbrain development "anomaly in the formation of or the patterning of the part of the brainstem developing from the middle of the three primary cerebral vesicles of the embryo" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0003935 abnormal craniofacial development "anomaly in the process of forming the face and/or cranium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0003944 abnormal T cell subpopulation ratio "deviation from the standard ratios of T cell subpopulations (e.g. double positive to single positive ratio) compared to control samples" [mberry:Melissa Berry, Genetics Resources Curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004096 abnormal midbrain-hindbrain boundary development "anomaly in the formation of the midbrain-hindbrain domain, comprised of the mesencephalic vesicle and the first rhombencephalic vesicle at early somitogenesis stages; an organizing center at the boundary patterns the midbrain and hindbrain primordia of the neural plate" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0004126 thin hypodermis "reduced thickness of the innermost and thickest layer of the skin composed of loose connective tissue containing adipoctyes" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004947 skin inflammation "local accumulation of fluid, plasma proteins, and leukocytes in the skin" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004956 decreased thymus weight "reduction in the average weight of the primary lymphoid organ that is required for maturation of T cells" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005018 decreased T cell number "fewer than normal T cell numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005090 increased double-negative T cells count "greater than expected numbers of the subset of T cells found in the thymus that express neither CD4 nor CD8" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005092 decreased double-positive T cell count "less than the expected number of the subset of T cells found in the thymus that express both CD4 and CD8" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005221 abnormal rostral-caudal axis patterning "anomaly in the development or formation of the axis that runs from the head to the tail of the body" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Wlstm1.2Whsu/Wlstm1.2Whsu
Genetic Background: involves: 129S6/SvEvTac

 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]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0005348 increased T cell proliferation "increased clonal expansion of naive T cells in response to stimuli" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005425 increased macrophage count "greater than the normal numbers of macrophages" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, J:73418]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005501 abnormal skin physiology "atypical function of the membranous protective covering of the body" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005503 abnormal tendon morphology "structural anomaly of the fibrous bands or cords of connective tissue at the ends of muscle fibers that attach muscles to bones and other structures" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, J:45509]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0005504 abnormal ligament morphology "structural anomaly of the flexible bands of fibrous tissue that connect the articular extremities of bones " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, J:45509]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0005508 abnormal skeleton morphology "malformation of the bony framework of the body in vertebrates" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0005666 abnormal adipose tissue physiology "functional anomaly of the connective tissue composed of fat cells enmeshed in areolar tissue" [cwg:Carroll-Ann W. Goldsmith, Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings, 2003]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0006042 increased apoptosis "greater than normal programmed cell death" [RGD:Rat Genome Database submission, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0006101 absent tegmentum "absence or loss of the floor of the midbrain which extends from the substantia nigra to the level of the cerebral aqueduct" [smb:Susan M Bello, Mouse Genome Informatics Curator, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0006106 absent tectum "absence or loss of the rostral part of the midbrain roof" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 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]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0006279 abnormal limb development "anomaly in the formation of the limbs" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0006280 abnormal digit development "anomaly in the formation of the digits" [J:70592, MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0008052 abnormal serous gland morphology "any structural anomaly of glands that secrete watery albuminous material that often contains enzymes" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0008347 decreased gamma-delta T cell number "reduced number of immature or mature T cells expressing an gamma-delta T cell receptor complex" [CL:0000798, ISBN:0781735149]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0008859 abnormal hair cycle catagen phase "anomaly in the phase of the hair growth cycle during which cell proliferation ceases, the hair follicle shortens, and an anchored hair is produced" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Ctnnb1tm2Kem/Ctnnb1tm2Kem,Tg(Krt1-15-cre/PGR)22Cot/0
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL

 MP:0008934 absent choroid plexus "absence of the fringe of the tela choroidea of the brain ventricles" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA/J * SJL

Allelic Composition: Wlstm1.1Whsu/Wlstm1.1Whsu,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * CBA/J

 MP:0009111 pancreas hypoplasia "underdevelopment or reduced size of the pancreas, usually due to a reduced number of cells" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA/J * SJL

 MP:0009583 increased keratinocyte proliferation "increase in the expansion rate of keratinocytes by cell division" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0009795 epidermal spongiosis "intercellular edema within the epidermis" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0009931 abnormal skin appearance "skin that looks different from the usual state" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0010743 delayed suture closure "late onset of the fusion of the bones of the skull" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Rgs11tm1Lex/Rgs11tm1Lex,Rgs7tm1Cjch/Rgs7tm1Cjch
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6

 MP:0011015 decreased body surface temperature "reduced degree of heat natural to skin-environment interface of a living being" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0011084 partial lethality at weaning "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms at weaning age" [MGI:csmith]
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Allelic Composition: Wlstm1Xzg/Wlstm1Xzg,Tg(Prrx1-cre)1Cjt/0
Genetic Background: involves: C57BL/6J * SJL/J

 MP:0011092 complete embryonic lethality "death of all organisms of a given genotype in a population within the embryonic period prior to organogenesis (Mus: prior to E14)" [MGI:csmith]
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Allelic Composition: Gt(ROSA)26Sortm1.1(Wls/YFP)Mbtr/Gt(ROSA)26Sor+
Genetic Background: involves: C57BL/6

 MP:0011098 complete embryonic lethality during organogenesis "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
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Allelic Composition: Hsd11b1tm1.1Ggla/Hsd11b1tm1.1Ggla
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Wlstm1.2Whsu/Wlstm1.2Whsu
Genetic Background: involves: 129S6/SvEvTac

 MP:0011106 partial embryonic lethality before somite formation "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 the point of implantation and somite formation (Mus: E4.5 to less than E8)" [MGI:csmith]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,Tg(EIIa-cre)C5379Lmgd/0
Genetic Background: involves: 129S/SvEv * FVB/N * SJL

 MP:0012087 absent midbrain "absence of the brain region derived from the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions in the adult, including eye movement and coordination of auditory and visual reflexes" [MGI:anna]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA/J * SJL

 MP:0012133 absent midbrain-hindbrain boundary "absence of the midbrain-hindbrain domain of the embryonic brain that is comprised of the mesencephalic vesicle and the first rhombencephalic vesicle at early somitogenesis stages; normally, an organizing center located at the boundary patterns the midbrain and hindbrain primordia of the neural plate" [MGI:anna]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA/J * SJL

 MP:0012138 decreased forebrain size "size reduction or truncation of the anterior of the three primary divisions of the developing chordate brain or the corresponding part of the adult brain (in vertebrates, includes especially the cerebral hemispheres, the thalamus, and the hypothalamus and especially in higher vertebrates is the main control center for sensory and associative information processing, visceral functions, and voluntary motor functions)" [GO:0048853]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA/J * SJL

 MP:0012173 short rostral-caudal axis "length reduction or truncation of the axis that runs from the head to the tail of the body" [MGI:anna]
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Allelic Composition: Wlstm1.1Lan/Wlstm1.1Lan,H2afvTg(Wnt1-cre)11Rth/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA/J * SJL

 MP:0013588 small thymus medulla "decreased size of the inner area of thymus lobules" [MGI:Anna]
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Allelic Composition: Wlstm1.1Arte/Wlstm1.1Arte,Krt14tm1(cre)Wbm/Krt14+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000029462 Vps29 / Q9QZ88 / VPS29 retromer complex component / Q9UBQ0*  / reaction / complex
 ENSMUSG00000019804 Snx3 / sorting nexin 3 / O60493*  / complex / reaction
 ENSMUSG00000031696 Vps35 / Q9EQH3 / VPS35 retromer complex component / Q96QK1*  / reaction / complex
 ENSMUSG00000020078 P40336 / Vps26a / VPS26 retromer complex component A / O75436*  / reaction / complex






 

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