ENSMUSG00000021464


Mus musculus

Features
Gene ID: ENSMUSG00000021464
  
Biological name :Ror2
  
Synonyms : Q9Z138 / receptor tyrosine kinase-like orphan receptor 2 / Ror2
  
Possible biological names infered from orthology : Q01974
  
Species: Mus musculus
  
Chr. number: 13
Strand: -1
Band: B1
Gene start: 53109312
Gene end: 53286124
  
Corresponding Affymetrix probe sets: 10409282 (MoGene1.0st)   1423428_at (Mouse Genome 430 2.0 Array)   1457128_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000123362
Ensembl peptide - ENSMUSP00000021918
NCBI entrez gene - 26564     See in Manteia.
MGI - MGI:1347521
RefSeq - NM_013846
RefSeq Peptide - NP_038874
swissprot - E9PUN5
swissprot - Q9Z138
Ensembl - ENSMUSG00000021464
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 ror2ENSDARG00000076227Danio rerio
 ROR2ENSGALG00000015208Gallus gallus
 ROR2ENSG00000169071Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Ror1 / Q9Z139 / Inactive tyrosine-protein kinase transmembrane receptor ROR1 / Q01973* / receptor tyrosine kinase like orphan receptor 1*ENSMUSG0000003530557
Igf1r / insulin like growth factor 1 receptor / P08069*ENSMUSG0000000553319
Musk / Q61006 / Muscle, skeletal receptor tyrosine-protein kinase / O15146* / muscle associated receptor tyrosine kinase*ENSMUSG0000005728019
Ntrk2 / P15209 / BDNF/NT-3 growth factors receptor / Q16620* / neurotrophic receptor tyrosine kinase 2*ENSMUSG0000005525419
Ntrk3 / Q6VNS1 / NT-3 growth factor receptor / Q16288* / neurotrophic receptor tyrosine kinase 3*ENSMUSG0000005914618
Ntrk1 / Q3UFB7 / High affinity nerve growth factor receptor / P04629* / neurotrophic receptor tyrosine kinase 1*ENSMUSG0000002807218
Insr / P15208 / Insulin receptor Insulin receptor subunit alpha Insulin receptor subunit beta / P06213* / insulin receptor*ENSMUSG0000000553418
Ros1 / Q78DX7 / Proto-onco tyrosine-protein kinase ROS / P08922* / ROS proto-oncogene 1, receptor tyrosine kinase*ENSMUSG0000001989318
Alk / P97793 / ALK tyrosine kinase receptor / Q9UM73* / ALK receptor tyrosine kinase*ENSMUSG0000005547117
Insrr / Q9WTL4 / Insulin receptor-related protein Insulin receptor-related protein alpha chain Insulin receptor-related protein beta chain / P14616* / insulin receptor related receptor*ENSMUSG0000000564017
Ddr2 / Q62371 / Discoidin domain-containing receptor 2 / Q16832* / discoidin domain receptor tyrosine kinase 2*ENSMUSG0000002667416
Ltk / P08923 / Leukocyte tyrosine kinase receptor / P29376* / leukocyte receptor tyrosine kinase*ENSMUSG0000002729715
Ddr1 / Q03146 / Epithelial discoidin domain-containing receptor 1 / Q08345* / discoidin domain receptor tyrosine kinase 1*ENSMUSG0000000353415
Ptk7 / Q8BKG3 / Inactive tyrosine-protein kinase 7 / Q13308* / protein tyrosine kinase 7 (inactive)*ENSMUSG0000002397214


Protein motifs (from Interpro)
Interpro ID Name
 IPR000001  Kringle
 IPR000719  Protein kinase domain
 IPR001245  Serine-threonine/tyrosine-protein kinase, catalytic domain
 IPR003598  Immunoglobulin subtype 2
 IPR003599  Immunoglobulin subtype
 IPR007110  Immunoglobulin-like domain
 IPR008266  Tyrosine-protein kinase, active site
 IPR011009  Protein kinase-like domain superfamily
 IPR013098  Immunoglobulin I-set
 IPR013783  Immunoglobulin-like fold
 IPR013806  Kringle-like fold
 IPR016247  Tyrosine-protein kinase, receptor ROR
 IPR018056  Kringle, conserved site
 IPR020067  Frizzled domain
 IPR036179  Immunoglobulin-like domain superfamily
 IPR036790  Frizzled cysteine-rich domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001501 skeletal system development IMP
 biological_processGO:0001502 cartilage condensation IMP
 biological_processGO:0001756 somitogenesis IMP
 biological_processGO:0006468 protein phosphorylation IEA
 biological_processGO:0007169 transmembrane receptor protein tyrosine kinase signaling pathway IEA
 biological_processGO:0007223 Wnt signaling pathway, calcium modulating pathway IPI
 biological_processGO:0007224 smoothened signaling pathway IMP
 biological_processGO:0007254 JNK cascade IDA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0008285 negative regulation of cell proliferation IEA
 biological_processGO:0014002 astrocyte development IEA
 biological_processGO:0016055 Wnt signaling pathway IEA
 biological_processGO:0016310 phosphorylation IEA
 biological_processGO:0018108 peptidyl-tyrosine phosphorylation IEA
 biological_processGO:0030154 cell differentiation IMP
 biological_processGO:0030282 bone mineralization IEA
 biological_processGO:0030335 positive regulation of cell migration IEA
 biological_processGO:0030509 BMP signaling pathway IMP
 biological_processGO:0030538 embryonic genitalia morphogenesis IMP
 biological_processGO:0030539 male genitalia development IEA
 biological_processGO:0042472 inner ear morphogenesis IMP
 biological_processGO:0042733 embryonic digit morphogenesis IMP
 biological_processGO:0043507 positive regulation of JUN kinase activity IEA
 biological_processGO:0045165 cell fate commitment IMP
 biological_processGO:0045651 positive regulation of macrophage differentiation IEA
 biological_processGO:0045893 positive regulation of transcription, DNA-templated IDA
 biological_processGO:0051968 positive regulation of synaptic transmission, glutamatergic IEA
 biological_processGO:0060071 Wnt signaling pathway, planar cell polarity pathway IMP
 biological_processGO:0060395 SMAD protein signal transduction IMP
 biological_processGO:0060828 regulation of canonical Wnt signaling pathway IMP
 biological_processGO:0090090 negative regulation of canonical Wnt signaling pathway IGI
 biological_processGO:0090263 positive regulation of canonical Wnt signaling pathway IDA
 biological_processGO:1900020 positive regulation of protein kinase C activity IEA
 biological_processGO:1905517 macrophage migration IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005874 microtubule IEA
 cellular_componentGO:0005886 plasma membrane TAS
 cellular_componentGO:0005887 integral component of plasma membrane ISS
 cellular_componentGO:0009986 cell surface IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0030425 dendrite IEA
 cellular_componentGO:0043025 neuronal cell body IEA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0004672 protein kinase activity IEA
 molecular_functionGO:0004714 transmembrane receptor protein tyrosine kinase activity TAS
 molecular_functionGO:0005109 frizzled binding IPI
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0016301 kinase activity IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0017147 Wnt-protein binding IEA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
WNT5A-dependent internalization of FZD2, FZD5 and ROR2


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000029 abnormal malleus morphology "structural anomaly in the largest of the three auditory ossicles, which resembles a club or hammer " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000042 abnormal organ of Corti "abnormalities associated with the highly specialized epithelium in the floor of the ductus cochlearis; also referred to a spiral organ (organum spirale), or acoustic papilla" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd

 MP:0000060 delayed bone ossification "late onset of the formation of bone" [J:40203]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000088 short mandible "reduced length of the lower bony framework of the mouth where the inferior teeth are held" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0000102 abnormal nasal bone morphology "malformed elongated rectangular bone that forms part of the nasal bridge" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17489]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0000137 abnormal vertebrae morphology "malformed bony segment of the spinal column" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0000150 abnormal rib morphology "malformed bones forming the bony wall of the chest" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:50311]
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Allelic Composition: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

 MP:0000154 rib fusion "appearance of one or more ribs as a single structure" [J:62022, J:62023]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0000158 absent sternum "missing long flat bone of the chest; articulates with clavicle and first seven rib pairs" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:62577]
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Allelic Composition: Ror1tm1Ymi/Ror1tm1Ymi,Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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]
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Allelic Composition: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

Allelic Composition: Ror1tm1Ymi/Ror1tm1Ymi,Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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]
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Allelic Composition: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

Allelic Composition: Ror1tm1Ymi/Ror1tm1Ymi,Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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]
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Allelic Composition: Ror1tm1Ymi/Ror1tm1Ymi,Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

 MP:0000441 wide skull 
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Allelic Composition: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

 MP:0000445 short snout "reduced length of the anterior facial part of the muzzle" [J:53370]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0000454 abnormal jaw morphology "malformation of the bony framework of the mouth where the teeth are held" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

 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: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

 MP:0000458 abnormal mandible morphology "malformation of the lower bony framework of the mouth where the inferior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

 MP:0000547 short limbs "reduced average length of the extremities" [MGI:CLS, J:61509]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2Tn(pb-ZG-s)1.1Mrc/Ror2Tn(pb-ZG-s)1.1Mrc
Genetic Background: involves: C57BL/6J

Allelic Composition: Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

Allelic Composition: Ror1tm1.2Meg/Ror1tm1.2Meg,Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

 MP:0000552 abnormal radius morphology "malformation of the short bone of the lateral forearm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 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]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0000559 abnormal femur morphology "structural anomaly of the long bone of the thigh" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0000562 polydactyly "greater than 5 digits on one or more autopods" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * 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: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

 MP:0000585 kinked tail "a sharp bend or zig-zag in the tail" [J:61295]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0000592 short tail "reduced length of tail compared to control " [J:55583]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror2Tn(pb-ZG-s)1.1Mrc/Ror2Tn(pb-ZG-s)1.1Mrc
Genetic Background: involves: C57BL/6J

 MP:0000914 exencephaly "neurocranial defects resulting in exposure or extrusion of the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
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Allelic Composition: Ror1tm1.2Meg/Ror1tm1.2Meg,Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

 MP:0001153 small seminiferous tubules "reduced diameter of the tubules in the testes where spermatogenesis occurs" [J:50844]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0001258 decreased body length "decreased crown to tail distance compared to controls" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0001300 ocular hypertelorism "increased distance between the eyes " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001349 excessive tearing "an unusually high amount of fluid secreted by the lacrimal glands, often resulting in overflow of fluid from the eye" [hdene:Howard Dene, Mouse Genome Informatics Curator, J:38104]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001688 abnormal somite development "anomalous formation of any of the paired, metamerically arranged cell masses formed in the embryonic paraxial mesoderm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001691 abnormal somite shape "atypical characteristic surface configuration of a segmental mass along the notochord of the developing embryo" [J:37888]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001698 reduced embryo size "smaller proportions of embryo compared to littermates" [J:61790]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001919 abnormal reproductive system physiology "anomaly in the function of the organs associated with producing offspring " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+,Tacc3tm1.1Tno/Tacc3+,Trp53tm1Tyj/Trp53tm1Tyj
Genetic Background: involves: 129S2/SvPas * 129S4/SvJae * C57BL/6

 MP:0001922 reduced male fertility "reduced ability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61340]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0001923 reduced female fertility "reduced ability of female to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409]
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Allelic Composition: Pgrtm2(cre)Lyd/Pgr+,Ror1tm1.1Meg/Ror1tm1.1Meg,Ror2tm1.1Meg/Ror2tm1.1Meg
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ

 MP:0001935 reduced litter size "fewer live born pups in a litter compared to average" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Hcfc1tm1Lwh/Hcfc1tm1Lwh,Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic Background: involves: C57BL/6 * CBA

 MP:0001954 respiratory distress "physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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: Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+,Tacc3tm1.1Tno/Tacc3+,Trp53tm1Tyj/Trp53tm1Tyj
Genetic Background: involves: 129S2/SvPas * 129S4/SvJae * C57BL/6

 MP:0002109 abnormal limb morphology "abnormal development of limbs resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Igf1rtm1Arge/Igf1rtm2Arge,Tg(Camk2a-cre)2Szi/0
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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: Rpl38Ts/Rpl38+
Genetic Background: BALB/c-Rpl38Ts

 MP:0002111 abnormal tail morphology "abnormal development of the tail resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0002113 abnormal skeleton development "anomalous differentiation or remodeling of bone tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0002114 abnormal axial skeleton morphology "abnormal development of vertebral, spinal or sternal bones resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0002192 hydrops fetalis "an abnormal accumulation of serous fluid in fetal tissues" [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: Ror1tm1.2Meg/Ror1tm1.2Meg,Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

 MP:0002216 abnormal seminiferous tubule morphology "malformation of the tubules in the testes where spermatogenesis occurs" [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: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0002270 abnormal alveoli morphology "any structural anomaly of the outpouching of the respiratory system where gas exchange occurs" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

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

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd

 MP:0002544 brachydactyly "abnormally short digits" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0002622 abnormal cochlear hair cell morphology "malformation of the sensory epithelial cells of the cochlea; these cells are in synaptic contact with the auditory nerve" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd

 MP:0002687 oligozoospermia "reduced concentration of spermatozoa " [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:57312]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0002759 abnormal caudal vertebrae morphology "malformed bony segments of the tail, usually 27-30 present" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:82849]
Show

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/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]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0002896 abnormal bone mineralization "defect in the process by which minerals are deposited into bone" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0002982 abnormal germ cell migration "defects in the orderly movement of a germ cell, a cell specialized to produce haploid gametes, from one site to another during development" [ava:Anna V. Anagnostopoulos , Mouse Genome Informatics Curator]
Show

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror2Y324C/Ror2Y324C
Genetic Background: involves: C57BL/6J

Allelic Composition: Baxtm1Sjk/Baxtm1Sjk,Ror2Y324C/Ror2Y324C
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0003047 abnormal thoracic vertebrae morphology "malformation of any or all of the thirteen bony segments of the spine located anterior to the lumbar vertebrae and posterior to the cervical vertebrae" [MeSH:National Library of Medicine - Medical Subject Headings, 2003, csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0003050 abnormal sacral vertebrae morphology "malformation of any or all of the four bony segments of the spine located posterior to the lumbar vertebrae and anterior to the caudal vertebrae" [MeSH:National Library of Medicine - Medical Subject Headings, 2003, csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003055 abnormal epiphyseal plate morphology "malformed or absent cartilagenous center of ossification on the long bones permitting growth of the bone in both directions during development" [MeSH:National Library of Medicine - Medical Subject Headings, 2003]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0003109 short femur "reduced length of the long bone of the thigh" [ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator, Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

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

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0003409 decreased width of hypertrophic chondrocyte zone "decreased width of cartilage cell matrix layer " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

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

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

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

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003723 abnormal long bone morphology "malformation of any of the several elongated bones of the extremities " [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror1tm1Ymi/Ror1tm1Ymi,Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003743 abnormal facial morphology "anomalous structure or development of the face" [ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

Allelic Composition: Ror1tm1.2Meg/Ror1tm1.2Meg,Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

 MP:0003854 abnormal forelimb stylopod morphology 
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003855 abnormal forelimb zeugopod morphology 
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003856 abnormal hindlimb stylopod morphology 
Show

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003857 abnormal hindlimb zeugopod morphology 
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003935 abnormal craniofacial development "anomaly in the process of forming the face and/or cranium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003960 increased lean body mass "more than average fat-free physical bulk or volume of the body including all its components except adipose tissue" [honda:Hiraoki Onda, Mouse GEnome Informatics Curator]
Show

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0004073 caudal body truncation "caudal part of body truncated with anterior portion relatively normal" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

Allelic Composition: Ror1tm1.2Meg/Ror1tm1.2Meg,Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

 MP:0004110 transposition of great arteries "cardiovascular malformation in which the aorta arises from the right ventricle while the pulmonary artery arises from the left ventricle" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
Show

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror1tm1Ymi/Ror1tm1Ymi,Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004173 abnormal intervertebral disk morphology "malformation of the cartilagenous and gelatinous structure found between vertebrae" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0004256 abnormal maternal decidual layer morphology "anomaly in the structure of the maternal uterine-derived portion of the placenta" [PMID:11433360]
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Allelic Composition: Pgrtm2(cre)Lyd/Pgr+,Ror1tm1.1Meg/Ror1tm1.1Meg,Ror2tm1.1Meg/Ror2tm1.1Meg
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ

 MP:0004351 short humerus "reduced length of one or both of the bones of the forelimb that articulates with the scapula above and the radius and ulna below" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

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

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004359 short ulna "reduced length of the medial and larger of the two bones of the forearm" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004399 abnormal cochlear outer hair cell morphology "any structural abnormality in the sensory cells of the organ of Corti which are in synaptic contact with sensory as well as efferent fibers of the auditory nerve; there are three rows of columnar outer hair cells largely surrounded by cortilymph and supporting phalangeal cells; the apical end of each cell is anchored to the cuticular plate and about 100 stereocilia arranged in a V-shaped pattern extend from the cell s surface through the cuticular plate into the tectorial membrane" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd

 MP:0004471 short nasal bone "reduced length of either of two rectangular bone plates forming the bridge of the nose" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0004472 broad nasal bone "increased width of either of two rectangular bone plates forming the bridge of the nose" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0004506 abnormal pubic bone morphology "any structural anomaly in the forward portion of either of the hipbones, at the juncture forming the front arch of the pelvis" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror1tm1Ymi/Ror1tm1Ymi,Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004595 abnormal mandibular condyloid process morphology "any structural anomaly of the round bump of bone and constricted neck portion that arises from the upper surface of the mandibular ramus (perpendicular portion) and articulates with the articular disk of the temporomandibular joint" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004596 abnormal mandibular angle morphology "any structural anomaly of the portion of the mandible where the body of the mandible (horizontal portion) and the rami (perpendicular portions) meet; these normally unite nearly at right angles" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004619 caudal vertebral fusion "the union of one or more caudal vertebrae into a single structure in species where this does not normally occur" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0004622 sacral vertebral fusion "the union of one or more sacral vertebrae into a single structure in species where this does not normally occur" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004634 short metacarpal bones "reduced length of the five bones of the forepaws that articulate proximally with the carpal bones and distally with the phalanges" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0004652 small caudal vertebrae "reduced size of the bony segments of the coccyx or tail; there are usually 27-30 present in rodents and only 3-5 fused vertebrae in human" [MESH:National Library of Medicine_Medical Subject Headings]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0004657 small sacral vertebrae "reduced size of any or all of the four bony segments of the spine located posterior to the lumbar vertebrae and anterior to the caudal vertebrae" [MESH:National Library of Medicine_Medical Subject Headings]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004667 vertebral body hypoplasia "underdevelopment or reduced size, usually due to a reduced number of cells, of the main cylindrical portion of the vertebra ventral to the vertebral canal" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0004686 decreased length of long bones "reduced end-to-end length of the several elongated bones of the extremities" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004703 abnormal vertebral column "any structural anomaly of the complete structure forming the rostral-caudal axis of the skeleton formed from the alternating segments of vertebra and intervertebral discs which support the spinal cord" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0004708 short lumbar vertebrae "reduced length of any or all of the six bony segments of the spine located anterior to the sacral vertebrae and posterior to the thoracic vertebrae" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0004726 abnormal nasal capsule morphology "any structural abnormality in the cartilage around the developing nasal cavity of the embryo" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004852 decreased testis weight "reduced average weight of the male reproductive glands" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0005105 abnormal middle ear ossicle morphology "anomalous structure or development of the three small bones of the middle ear" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0005222 abnormal somite size "atypical size of any of the segmental masses along the notochord of the developing embryo" [J:72325]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005225 abnormal vertebrae development "anomalous formation of the vertebrae from the sclerotome" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0005296 abnormal humerus morphology "malformation of the bone of the forelimb that articulates with the scapula above and the radius and ulna below" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0005306 abnormal phalanx morphology "aberrant structure of any of the long bones of the digits" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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: Ror2Tn(pb-ZG-s)1.1Mrc/Ror2Tn(pb-ZG-s)1.1Mrc
Genetic Background: involves: C57BL/6J

 MP:0005587 abnormal Meckel s cartilage morphology "structural anomaly of this cartilage bar in the mandibular arch that forms a temporary supporting structure in the embryonic mandible; gives rise to middle ear bones and sphenomandibular and anterior malleolar ligaments" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17694]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0006165 entropion "abnormal inward rolling of the eyelid, most commonly the lower lid" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0006212 large orbits "increased size of the orbits" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0006281 abnormal tail development "anomaly in the formation of the tail" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2Y324C/Ror2Y324C
Genetic Background: involves: C57BL/6J

 MP:0008272 abnormal endochondral bone ossification "anomaly in the process of the formation of bone by the replacement of cartilage tissue with mineralized bone" [GO:0001958]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0008391 abnormal primordial germ cell morphology "any structural anomaly of a mesodermally-derived, most primitive undifferentiated sex cell, that originates in the allantois and migrates through the hindgut and into the gonadal ridge" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Baxtm1Sjk/Baxtm1Sjk,Ror2Y324C/Ror2Y324C
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0008392 decreased primordial germ cell number "reduced number of a mesodermally-derived, most primitive undifferentiated sex cell, that originates in the allantois and migrates through the hindgut and into the gonadal ridge" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Ror2Y324C/Ror2Y324C
Genetic Background: involves: C57BL/6J

Allelic Composition: Baxtm1Sjk/Baxtm1Sjk,Ror2Y324C/Ror2Y324C
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0008786 abnormal hindgut morphology "any structural anomaly of the caudal portion of the primitive digestive tube of the embryo" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2Y324C/Ror2Y324C
Genetic Background: involves: C57BL/6J

 MP:0009284 abnormal sympathetic neuron innervation "defective or incomplete supply of nerve fibers to sympathetic termini" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror1tm1.2Meg/Ror1tm1.2Meg,Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

 MP:0009642 abnormal blood homeostasis "anomaly in the processes involved in the maintenance of an internal equilibrium of various functions or chemical or protein composition of the blood" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0009666 abnormal embryo attachment "any anomaly in the process whereby the blastocyst anchors to the uterine luminal epithelium and cannot be dislodged by flushing" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator", PMID:10882512 "Carson DD, et al, Embryo implantation Dev Biol. 2000 Jul 15;223(2):217-37."]
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Allelic Composition: Pgrtm2(cre)Lyd/Pgr+,Ror1tm1.1Meg/Ror1tm1.1Meg,Ror2tm1.1Meg/Ror2tm1.1Meg
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ

 MP:0009703 decreased birth body size "reduction in average body size at birth compared to controls" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2Tn(pb-ZG-s)1.1Mrc/Ror2Tn(pb-ZG-s)1.1Mrc
Genetic Background: involves: C57BL/6J

 MP:0009768 impaired somite development "atypical process of somite formation with the result of fewer or none of these cell masses being formed" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2Y324C/Ror2Y324C
Genetic Background: involves: C57BL/6J

 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]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0009890 cleft secondary palate "congenital fissure of the tissues normally uniting to form the secondary palate" [PMID:16680722]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0010025 decreased total body fat amount "less than the normal total amount of connective tissue composed of fat cells within the entire body" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0010402 ventricular septal defect "abnormal communications between the two lower chambers of the heart, including such defects in the perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular regions" [MESH:C14.240.400.560.540]
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Allelic Composition: Ror1tm1Ymi/Ror1tm1Ymi,Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0010418 perimembraneous ventricular septal defect "abnormal communications between the two lower chambers of the heart, occurring in the membranous septum with defects in the adjacent muscular portion of the septum; it is generally located in the LV outflow tract just below the aortic valve, associated with pouches or aneurysms of the septal leaflet of the tricuspid valve, which may partially or completely close the defect; an LV-to-RA shunt may also be associated with this defect" [http://emedicine.medscape.com]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0010869 decreased bone trabecula number "decreased number of intersecting plates and spicules in cancellous bone which form a meshwork of intercommunicating spaces filled with blood vessels and marrow; in mature bone, the trabeculae are aligned in parallel with the lines of major compressive or tensile force" [http://www.dorlands.com/ "Dorland s Illustrated Medical Dictionary, 31st edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 MP:0010879 decreased trabecular bone volume "decrease in the amount of space occupied by trabecular bone tissue in the skeleton" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Ror2tm1Anec/Ror2tm1Anec
Genetic Background: B6.129S1-Ror2tm1Anec

 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: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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]
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Allelic Composition: Leprdb/Leprdb
Genetic Background: involves: C57BLKS/J

 MP:0011090 partial perinatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith]
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Allelic Composition: Ror1tm1Ymi/Ror1tm1Ymi,Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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]
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Allelic Composition: Ror1tm1.2Meg/Ror1tm1.2Meg,Ror2tm1.2Meg/Ror2tm1.2Meg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * FVB/N

 MP:0011610 abnormal primordial germ cell apoptosis "change in the timing or the number of primordial germ cells undergoing programmed cell death" [MGI:smb]
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Allelic Composition: Ror2Y324C/Ror2Y324C
Genetic Background: involves: C57BL/6J

 MP:0011772 genital tubercle hypoplasia "underdevelopment or reduced size of the embryonic anlage of the external genitalia, usually due to a reduced number of cells" [MGI:anna]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0012062 small tail bud "decreased size or area of the primordial region of the embryo that arises to form the tail of the adult" [MGI:anna]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0012085 midface hypoplasia "underdevelopment of the midfacial region comprising the nasal, maxillary, and zygomatic bones, leading to a concave-looking face" [MGI:anna]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0013933 short Meckel s cartilage 
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0014106 delayed chondrocyte differentiation "delay in the process in which a chondroblast acquires specialized structural and/or functional features of a chondrocyte" [GO:0002062]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0030321 abnormal tegmen tympani morphology "any structural anomaly of the thin plate of bone which separates the middle ear (tympanic) cavity from the dura of the middle cranial fossa and forms the roof of the middle ear cavity; it is formed in part by the petrous portion of the temporal bone, and the squamous portion of the temporal bone" [http://www.drtbalu.com/anat_middleear.html, https://medical-dictionary.thefreedictionary.com/tegmen+tympani]
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Allelic Composition: Ror2tm1Ymi/Ror2tm1Ymi
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000021994 Wnt5a / P22725 / wingless-type MMTV integration site family, member 5A / P41221* / Wnt family member 5A*  / reaction / complex
 ENSMUSG00000026556 Q91ZD4 / Vangl2 / VANGL planar cell polarity 2 / Q9ULK5* / VANGL planar cell polarity protein 2*  / reaction / complex






 

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