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Integrated Animals is a virtual database currently indexing available animal strains and mutants from: AGSC (Ambystoma), BCBC (mice), BDSC (flies), European Xenopus Resource Center (frog), The National Xenopus Resource (frog), Xenopus Express (frog), CWRU Cystic Fibrosis Mouse Models (mice), DGGR (flies), FlyBase (flies), IMSR (mice), MGI (mice), MMRRC (mice), NSRRC (pig), RGD (rats), Sperm Stem Cell Libraries for Biological Research (rats), Tetrahymena Stock Center (Tetrahymena), WormBase (worms), XGSC (Xiphophorus), ZFIN (zebrafish), and ZIRC (zebrafish). Note, the IMSR data is linked, but users may need to re-execute the search if the top mouse is not returned properly.
Note: BCBC is no longer in service, so the links may not be functional.

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  • Background:involves: 129s1/sv * 129x1/svj (facet)

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1,297 Results - per page

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Organism Name Proper Citation Species Synonyms Notes Phenotype Affected Gene Genomic Alteration Catalog Number Background Database Database Abbreviation Availability Source References Alternate IDs Record Last Update Mentions Count
Ica1tm1Mdos/Ica1tm1Mdos
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3831658 Mus musculus Allele Detail: Targeted This is a legacy resource. reproductive system phenotype, no abnormal phenotype detected Ica1 tm1Mdos 3831658 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:26306493
PMID:11751995
2024-01-30 12:18:55 0
Ctnnb1tm2Kem/Ctnnb1tm2.1Kem; Kdrtm1(cre)Sato/Kdr+
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3831190 Mus musculus Allele Detail: Targeted This is a legacy resource. abnormal vasculogenesis, embryonic lethality during organogenesis, complete penetrance, intracranial hemorrhage, spinal hemorrhage, abnormal blood-brain barrier function Kdr, Ctnnb1 tm2Kem, tm1(cre)Sato, tm2.1Kem 3831190 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:19023080 2024-01-30 12:19:41 0
Slc39a13tm1Thir/Slc39a13tm1Thir
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3829897 Mus musculus Allele Detail: Targeted This is a legacy resource. thickened long bone epiphysis, malocclusion, abnormal jaw morphology, abnormal long bone hypertrophic chondrocyte zone, small mandible, abnormal alveolar process morphology, brittle teeth, abnormal molar root morphology, abnormal bone structure, abnormal long bone epiphysis morphology, abnormal dermal layer morphology, abnormal epiphyseal plate morphology, abnormal long bone epiphyseal plate proliferative zone, kyphosis, abnormal eyelid aperture, decreased cornea thickness, abnormal trabecular bone morphology, decreased length of long bones, enophthalmos, abnormal tooth morphology, abnormal osteoblast physiology, abnormal incisor morphology, small maxilla, abnormal long bone morphology, abnormal long bone metaphysis morphology, decreased bone mineral density, decreased compact bone thickness, postnatal growth retardation Slc39a13 tm1Thir 3829897 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:18985159 2024-01-30 12:19:42 0
Cdh1tm2Kem/Cdh1tm2Kem; Tg(Krt14-RNAi:Cdh3)1Efu; Tg(KRT14-cre)1Efu
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3830547 Mus musculus Allele Detail: Transgenic, Targeted This is a legacy resource. neonatal lethality, complete penetrance, abnormal epidermis stratum basale morphology, abnormal epidermal layer morphology, abnormal skin condition, impaired skin barrier function, shiny skin, decreased birth body size, abnormal skin physiology, abnormal epidermis stratum spinosum morphology, tight skin, abnormal epidermis suprabasal layer morphology, blistering, thick epidermis, decreased hair follicle number, flaky skin Cdh1 tm2Kem, Tg(Krt14-RNAi:Cdh3)1Efu, Tg(KRT14-cre)1Efu 3830547 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:18809908 2024-01-30 12:19:42 0
Fgfr2tm1Moon/Fgfr2+
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3829043 Mus musculus Allele Detail: Targeted This is a legacy resource. no phenotypic analysis Fgfr2 tm1Moon 3829043 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:18832392 2024-01-30 12:18:57 0
Fermt1tm1Ref/Fermt1tm1Ref
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3828513 Mus musculus Allele Detail: Targeted This is a legacy resource. thin epidermis, large intestinal inflammation, increased urine osmolality, renal/urinary system phenotype, increased urine protein level, postnatal lethality, complete penetrance, distended ileum, skin atrophy, abnormal colon morphology, abnormal ileum morphology, abnormal intestine morphology, ileum inflammation, decreased keratinocyte adhesion, distended stomach, dehydration, decreased keratinocyte proliferation, postnatal growth retardation Fermt1 tm1Ref 3828513 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:19057668 2024-01-30 12:18:57 0
Tspan33tm1Stsa/Tspan33tm1Stsa
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3826392 Mus musculus Allele Detail: Targeted This is a legacy resource. enlarged spleen, increased liver tumor incidence, decreased hematocrit, thrombocytopenia, abnormal splenic cell ratio, extramedullary hematopoiesis, abnormal erythrocyte morphology, leptocytosis, decreased erythrocyte cell number, macrocytosis, increased monocyte cell number, abnormal spleen morphology, anemia, reticulocytosis Tspan33 tm1Stsa 3826392 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:17158226 2024-01-30 12:18:57 0
Lama5tm3Jhm/Lama5tm3Jhm
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3823250 Mus musculus Allele Detail: Targeted This is a legacy resource. polycystic kidney, enlarged kidney, increased blood urea nitrogen level, increased urine protein level, renal interstitial fibrosis, increased kidney apoptosis, dilated renal tubules, decreased body size, abnormal renal glomerulus basement membrane morphology, kidney failure, premature death Lama5 tm3Jhm 3823250 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:16790509 2024-01-30 12:18:57 0
Prkg2tm1Pfe/Prkg2+
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3826804 Mus musculus Allele Detail: Targeted This is a legacy resource. Prkg2 tm1Pfe 3826804 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center 2024-01-30 12:18:57 0
Pdgfctm1Nagy/Pdgfctm1Nagy
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3511132 Mus musculus Allele Detail: Targeted This is a legacy resource. neonatal lethality, incomplete penetrance, short nasal septum, blistering, edema, postnatal lethality, complete penetrance, cleft secondary palate, abnormal palate bone morphology, palatal shelf hypoplasia, failure of palatal shelf elevation, abnormal palatal shelf fusion at midline, spina bifida occulta Pdgfc tm1Nagy 3511132 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:15361870 2024-01-30 12:20:31 0
Pdgfatm1Cbet/Pdgfatm1Cbet; Pdgfctm1Nagy/Pdgfctm1Nagy
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3511133 Mus musculus Allele Detail: Targeted This is a legacy resource. rib bifurcation, spina bifida, short sternum, blistering, abnormal somite development, abnormal myotome development, abnormal axial skeleton morphology, decreased embryo size, midline facial cleft, wavy neural tube, embryonic lethality during organogenesis, complete penetrance, pericardial effusion, abnormal craniofacial bone morphology, abnormal kidney cortex morphology, hydrops fetalis, common atrium, abnormal scapula morphology, rib fusion Pdgfc, Pdgfa tm1Nagy, tm1Cbet 3511133 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:15361870 2024-01-30 12:20:31 0
Slc1a3tm1Wst/Slc1a3tm1Wst
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3056590 Mus musculus Allele Detail: Targeted This is a legacy resource. abnormal excitatory postsynaptic currents Slc1a3 tm1Wst 3056590 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:15363892 2024-01-30 12:20:32 0
Miatm1Rbu/Miatm1Rbu
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3055025 Mus musculus Allele Detail: Targeted This is a legacy resource. abnormal chondrocyte morphology, integument phenotype, skeleton phenotype, endocrine/exocrine gland phenotype Mia tm1Rbu 3055025 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:11839810 2024-01-30 12:20:33 0
Adora1tm1Jgsc/Adora1tm1Jgsc
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3055093 Mus musculus Allele Detail: Targeted This is a legacy resource. abnormal response/metabolism to endogenous compounds Adora1 tm1Jgsc 3055093 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:15343381 2024-01-30 12:20:33 0
Sox11tm1Weg/Sox11tm1Weg
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3053114 Mus musculus Allele Detail: Targeted This is a legacy resource. decreased pulmonary respiratory rate, cyanosis, decreased birth weight, abnormal rib morphology, abnormal caudal vertebrae morphology, abnormal lumbar vertebrae morphology, asymmetric sternocostal joints, increased rib number, abnormal phalanx morphology, abnormal talus morphology, abnormal calcaneum morphology, curly tail, abnormal pancreas morphology, abnormal stomach pyloric region morphology, abnormal sternum ossification, omphalocele, small stomach, abnormal truncus arteriosus septation, palatal shelves fail to meet at midline, barrel chest, neonatal lethality, complete penetrance, absent spleen, maxilla hypoplasia, abnormal bone ossification, abnormal sternebra morphology, cleft palate, cleft upper lip, abnormal pterygoid process morphology, ventricular septal defect, persistent truncus arteriosis, abnormal eyelid morphology, abnormal bronchus morphology, pulmonary hypoplasia Sox11 tm1Weg 3053114 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:15254231 2024-01-30 12:20:34 0
Ptch1tm1Mps/Ptch1+; Disp1tm1Amc/Disp1tm1Amc
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3052724 Mus musculus Allele Detail: Targeted This is a legacy resource. no abnormal phenotype detected, nervous system phenotype Ptch1, Disp1 tm1Mps, tm1Amc 3052724 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:15269168 2024-01-30 12:20:34 0
Inatm1Jpj/Inatm1Jpj
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3052818 Mus musculus Allele Detail: Targeted This is a legacy resource. no abnormal phenotype detected Ina tm1Jpj 3052818 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:10350642 2024-01-30 12:20:34 0
Vegfatm1Pec/Vegfatm1Pec
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3047228 Mus musculus Allele Detail: Targeted This is a legacy resource. enlarged myocardial fiber, decreased neuron number, increased neuron apoptosis, abnormal blood vessel morphology, myocardial fiber degeneration, abnormal T wave, decreased capillary density, increased capillary tortuosity, abnormal neuronal migration, abnormal facial motor nucleus morphology, lethargy, dilated capillary, irregular heartbeat, hemorrhage, enlarged heart, decreased left ventricle systolic pressure, decreased heart rate, decreased cardiac muscle contractility, decreased body weight, decreased angiogenesis, cardiac ischemia, renal glomerulus hypertrophy, abnormal venule morphology, dilated capillary, neonatal lethality, incomplete penetrance, abnormal arteriole morphology, abnormal artery morphology, abnormal glomerular capillary endothelium morphology, abnormal sarcomere morphology, abnormal retinal vasculature morphology, pulmonary trunk hypoplasia, abnormal third pharyngeal arch artery morphology, abnormal capillary morphology, decreased lymphocyte cell number, abnormal thymus morphology, aorta pulmonary collateral arteries, thymus hypoplasia, abnormal vascular regression, short mandible, right aortic arch, abnormal blood vessel morphology, ventricular septal defect, absent incisors, persistent right dorsal aorta, absent parathyroid glands, athymia, interrupted aortic arch, ectopic thymus, abnormal capillary morphology, abnormal coronary artery morphology, retroesophageal right subclavian artery, persistent truncus arteriosis, cervical aortic arch, overriding aortic valve, double aortic arch, cleft palate, abnormal coronal suture morphology, cyanosis, abnormal heart morphology, abnormal mandible morphology, abnormal fourth pharyngeal arch artery morphology, abnormal pharyngeal arch artery morphology, abnormal coronary vessel morphology, abnormal carotid artery morphology, abnormal artery morphology, persistent ductus caroticus, abnormal kidney blood vessel morphology, abnormal retinal vasculature morphology, abnormal sixth pharyngeal arch artery morphology, persistence of hyaloid vascular system, retinal hemorrhage, small kidney, abnormal mesangial cell morphology, abnormal kidney interlobular artery morphology, increased circulating creatinine level, abnormal loop of Henle morphology, abnormal kidney arterial blood vessel morphology, abnormal renal glomerulus basement membrane thickness, abnormal myocardial fiber morphology, increased blood urea nitrogen level, renal ischemia, abnormal glomerular capillary morphology, glomerulosclerosis, expanded mesangial matrix, abnormal kidney afferent arteriole morphology, abnormal renal glomerulus basement membrane morphology, abnormal proximal convoluted tubule morphology, decreased glomerular capillary number, decreased renal glomerular filtration rate, abnormal peritubular capillary morphology, abnormal pericyte morphology, dilated proximal convoluted tubules, pale kidney, prolonged QRS complex duration, abnormal kidney efferent arteriole morphology, decreased renal glomerulus number, abnormal kidney blood vessel morphology, abnormal impulse conducting system conduction, abnormal coronary artery morphology, abnormal cardiac muscle relaxation, abnormal capillary morphology, abnormal ST segment, abnormal nephrogenic zone morphology, thick pulmonary interalveolar septum, respiratory distress, atelectasis, prolonged QT interval, postnatal lethality, complete penetrance, abnormal heart morphology, neonatal lethality, incomplete penetrance, abnormal lung development, abnormal cardiovascular system physiology Vegfa tm1Pec 3047228 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:15545635
PMID:11827992
PMID:21828096
PMID:12039984
PMID:12539040
PMID:12053176
PMID:10229225
2024-01-30 12:20:36 0
Nox1tm1Cyn
 
Resource Report

The record is no longer available at this source.
RRID:MGI:3695722 Mus musculus Allele Detail: Targeted This is a legacy resource. abnormal redox activity, decreased systemic arterial blood pressure, abnormal vasodilation, abnormal cytokine secretion, impaired wound healing, decreased cell migration Nox1 tm1Cyn 3695722 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:23749776
PMID:16246966
2024-01-30 12:19:50 0
Ptf1atm1.1(cre)Cvw/Ptf1atm1.1(cre)Cvw
 
Resource Report

1+ mentions
The record is no longer available at this source.
RRID:MGI:3695166 Mus musculus Allele Detail: Targeted This is a legacy resource. thick retinal ganglion layer, absent horizontal cells, increased retinal ganglion cell number, abnormal retina morphology, absent amacrine cells, absent retinal inner plexiform layer, abnormal eye development, absent pancreas, neonatal lethality, complete penetrance Ptf1a tm1.1(cre)Cvw 3695166 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:17075007
PMID:18198335
2024-01-30 12:19:51 1

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