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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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1,221,723 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
Hprttm5Detl/Hprttm5Detl
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668526 Mus musculus Allele Detail: Targeted This is a legacy resource. behavior/neurological phenotype Hprt tm5Detl 2668526 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12812988 2024-01-30 12:20:58 0
Gli3TgBR/Gli3+
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668574 Mus musculus Allele Detail: Transgenic This is a legacy resource. preaxial polydactyly, hydrocephaly Gli3 TgBR 2668574 involves: C57BL/6J MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12112872 2024-01-30 12:20:58 0
Ring1tm1Mvi/Ring1+
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668212 Mus musculus Allele Detail: Targeted This is a legacy resource. vertebral transformation, abnormal cervical atlas morphology, abnormal vertebrae morphology, abnormal cervical axis morphology Ring1 tm1Mvi 2668212 involves: 129P2/OlaHsd * BALB/c MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:11060235 2024-01-30 12:21:29 0
Npm2tm1Zuk/Npm2tm1Zuk
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668732 Mus musculus Allele Detail: Targeted This is a legacy resource. decreased litter size, abnormal oocyte morphology, reduced female fertility, abnormal embryonic tissue morphology Npm2 tm1Zuk 2668732 involves: 129 * C57BL/6J MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12714744 2024-01-30 12:20:58 0
Prdx2tm1Yu/Prdx2tm1Yu
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668457 Mus musculus Allele Detail: Targeted This is a legacy resource. increased spleen red pulp amount, increased cellular sensitivity to hydrogen peroxide, echinocytosis, decreased hemoglobin content, decreased hematocrit, abnormal erythropoiesis, reticulocytosis, increased spleen weight, hemolytic anemia, abnormal proerythroblast morphology, abnormal bone marrow cell morphology/development, increased cellular sensitivity to oxidative stress, increased number of Heinz bodies, schistocytosis, enlarged spleen, abnormal erythrocyte morphology, hemosiderosis, spherocytosis Prdx2 tm1Yu 2668457 involves: 129S4/SvJae MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12586629 2024-01-30 12:20:58 0
Map4Gt(pGT1.8geo)2Pgr/Map4Gt(pGT1.8geo)2Pgr
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668612 Mus musculus Allele Detail: Gene trapped This is a legacy resource. no abnormal phenotype detected Map4 Gt(pGT1.8geo)2Pgr 2668612 involves: 129 MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:9626500 2024-01-30 12:21:45 0
Tgfb2tm1Doe/Tgfb2tm1Doe
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668213 Mus musculus Allele Detail: Targeted This is a legacy resource. atelectasis, decreased corneal stroma thickness, neonatal lethality, complete penetrance, abnormal eye anterior chamber morphology, persistence of hyaloid vascular system, abnormal iris stroma morphology, abnormal cornea posterior stroma morphology, inlet ventricular septal defect, small temporal bone, abnormal semilunar valve morphology, small parietal bone, large fontanelles, patent aortic valve, increased urine protein level, abnormal renal tubule epithelium morphology, abnormal macrophage physiology, small olecranon, small mandibular condyloid process, ascending aorta hypoplasia, absent deltoid tuberosity, absent Rosenthal canal, absent spiral limbus, absent interdental cells, abnormal scala vestibuli morphology, abnormal cochlear ganglion morphology, abnormal kidney morphology, dilated renal tubules, absent kidney, abnormal cochlea morphology, ectopic adrenal gland, abnormal uterine horn morphology, patent pulmonary valve, abnormal thoracic cage shape, absent mandibular angle, abnormal semilunar valve morphology, persistent right dorsal aorta, abnormal heart ventricle outflow tract morphology, absent occipital bone, abnormal mandible morphology, failure of heart looping, abnormal heart septum morphology, heart valve hyperplasia, dilated heart right ventricle, abnormal atrioventricular cushion morphology, ostium primum atrial septal defect, failure of atrioventricular cushion closure, abnormal myocardium layer morphology, abnormal atrioventricular valve morphology, abnormal craniofacial bone morphology, absent pterygoid process, absent alisphenoid bone, trabecula carnea hypoplasia, double outlet right ventricle, failure of palatal shelf elevation, double inlet heart left ventricle, dilated heart right ventricle, absent Descemet membrane, abnormal corneal stroma morphology, absent corneal endothelium, decreased cornea thickness, abnormal retinal neuronal layer morphology, fused cornea and lens, vitreous body deposition, rib fusion, decreased corneal stroma thickness, abnormal eye posterior chamber morphology, retina hyperplasia, perinatal lethality, incomplete penetrance, ascending aorta hypoplasia, abnormal cardiac outflow tract development, complete atrioventricular septal defect, abnormal aorta morphology, aortic arch hypoplasia, thick aortic valve cusps, ectopic testis, testis hypoplasia, hydronephrosis, atrioventricular septal defect, abnormal cardiovascular development, thick mitral valve, thick tricuspid valve, aberrant origin of the right subclavian artery, thick pulmonary valve cusps, pulmonary artery hypoplasia, neonatal lethality, complete penetrance, abnormal truncus arteriosus septation, interrupted aortic arch, double outlet right ventricle, small mandibular coronoid process, abnormal limb morphology, abnormal trochanter morphology, abnormal femur morphology, short mandible, abnormal humerus morphology, inlet ventricular septal defect, cleft secondary palate, retrognathia, small interparietal bone, small frontal bone, abnormal myocardium layer morphology, abnormal neurocranium morphology, absent maxillary shelf, abnormal atrioventricular valve morphology, short ulna, cyanosis, decreased body weight, short radius, spina bifida occulta, abnormal rib morphology, abnormal sternum morphology, dilated respiratory conducting tubes, respiratory distress, abnormal clavicle morphology, abnormal xiphoid process morphology, perimembraneous ventricular septal defect Tgfb2 tm1Doe 2668213 involves: 129P2/OlaHsd * Black Swiss MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:11390347
PMID:9217007
PMID:11784073
2024-01-30 12:20:58 0
Tgfb3tm1Jhg/Tgfb3tm1Jhg
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668698 Mus musculus Allele Detail: Targeted This is a legacy resource. cleft secondary palate, abnormal lung development, hemothorax, cyanosis, abnormal lung development, decreased type II pneumocyte number, abnormal pulmonary interalveolar septum morphology, decreased type II pneumocyte number, thick lung-associated mesenchyme, abnormal lung saccule morphology, atelectasis, abnormal pulmonary vein morphology, abnormal lung vasculature morphology, persistence of medial edge epithelium during palatal shelf fusion, abnormal pulmonary alveolus morphology, abnormal lung vasculature morphology, lung hemorrhage, impaired lung alveolus development, abnormal pulmonary elastic fiber morphology, abnormal suckling behavior, dilated respiratory conducting tubes, respiratory distress, thick lung-associated mesenchyme, absent gastric milk in neonates, neonatal lethality, complete penetrance, pulmonary hypoplasia Tgfb3 tm1Jhg 2668698 either: (involves: 129S1/Sv * 129X1/SvJ * Black Swiss) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:7493022
PMID:10600892
2024-01-30 12:20:58 0
Tgfb2tm1Doe/Tgfb2+
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668214 Mus musculus Allele Detail: Targeted This is a legacy resource. abnormal spermatogenesis, oligozoospermia, bulbourethral gland hyperplasia, abnormal bulbourethral gland morphology, teratozoospermia, prostate gland anterior lobe hyperplasia, abnormal bulbourethral gland physiology, cystic bulbourethral gland Tgfb2 tm1Doe 2668214 involves: 129P2/OlaHsd * Black Swiss MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12220125 2024-01-30 12:20:58 0
Il7tm1Hms/Il7tm1Hms
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668582 Mus musculus Allele Detail: Targeted This is a legacy resource. thymus hypoplasia, decreased bone marrow cell number, spleen hypoplasia Il7 tm1Hms 2668582 involves: 129S6/SvEvTac MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:9486111 2024-01-30 12:20:58 0
Sc5dtm1Fdp/Sc5dtm1Fdp
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668465 Mus musculus Allele Detail: Targeted This is a legacy resource. decreased birth weight, abnormal phalanx morphology, fetal growth retardation, perinatal lethality, complete penetrance, abnormal cholesterol homeostasis, interparietal bone hypoplasia, abnormal limb development, lysosomal protein accumulation, mandible hypoplasia, increased liver weight, decreased cholesterol level, skin edema, decreased glycogen level, abnormal brown adipose tissue morphology, abnormal pancreatic acinar cell zymogen granule morphology, atelectasis, decreased brain cholesterol level, abnormal mandibular dental arch morphology, narrow frontonasal prominence, polydactyly, thin ribs, bowed radius, bowed tibia, bowed ulna, cleft palate, kinked tail, micrognathia, short limbs, abnormal neurocranium morphology, abnormal autopod morphology Sc5d tm1Fdp 2668465 involves: 129S1/Sv * 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12812989 2024-01-30 12:20:58 0
Celsr1Crsh/Celsr1Crsh
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668349 Mus musculus Allele Detail: Chemically induced (ENU) This is a legacy resource. abnormal outer hair cell kinocilium location or orientation, craniorachischisis, incomplete rostral neuropore closure, absent eyelids, abnormal orientation of outer hair cell stereociliary bundles, perinatal lethality, complete penetrance, abnormal cochlear sensory epithelium morphology, craniorachischisis Celsr1 Crsh 2668349 involves: 101/H * BALB/c * C3H/HeH MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12842012
PMID:25128525
2024-01-30 12:20:58 0
Cnmdtm1Ref/Cnmdtm1Ref
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668196 Mus musculus Allele Detail: Targeted This is a legacy resource. no abnormal phenotype detected Cnmd tm1Ref 2668196 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12192060 2024-01-30 12:20:58 0
Engtm1Mle/Eng+
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2669003 Mus musculus Allele Detail: Targeted This is a legacy resource. hemorrhage, ruffled hair, ear telangiectases, weight loss, neck telangiectases, respiratory distress, internal hemorrhage, tail telangiectases Eng tm1Mle 2669003 involves: 129P2/OlaHsd * C57BL/6 MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:10562296 2024-01-30 12:20:58 0
Ccr8tm1Gma/Ccr8tm1Gma
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668550 Mus musculus Allele Detail: Targeted This is a legacy resource. no abnormal phenotype detected Ccr8 tm1Gma 2668550 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12574386 2024-01-30 12:20:58 0
Rasgrf1tm1Esn/Rasgrf1tm1Esn
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2669007 Mus musculus Allele Detail: Targeted This is a legacy resource. decreased body weight, impaired glucose tolerance, small pancreatic islets, decreased circulating insulin level, decreased total body fat amount, decreased pancreatic beta cell number, enhanced lipolysis Rasgrf1 tm1Esn 2669007 involves: 129/Sv * C57BL/6N MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12805218 2024-01-30 12:20:58 0
Cd33tm1Avrk/Cd33tm1Avrk
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668832 Mus musculus Allele Detail: Targeted This is a legacy resource. increased circulating aspartate transaminase level, decreased inflammatory response, abnormal erythrocyte cell number Cd33 tm1Avrk 2668832 involves: 129X1/SvJ * C57BL/6 MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12773563 2024-01-30 12:20:58 0
Akap12Gt(ble-lacZ)15Brr/Akap12Gt(ble-lacZ)15Brr
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668554 Mus musculus Allele Detail: Gene trapped This is a legacy resource. no abnormal phenotype detected Akap12 Gt(ble-lacZ)15Brr 2668554 involves: 129S2/SvPas MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:11429284 2024-01-30 12:20:58 0
Wt1tm1Jae/Wt1tm1Jae
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2669009 Mus musculus Allele Detail: Targeted This is a legacy resource. absent adrenal gland, abnormal spleen development, absent spleen, pulmonary hypoplasia, increased splenocyte apoptosis, abnormal diaphragm development, diaphragmatic hernia, perinatal lethality, complete penetrance, prenatal lethality, incomplete penetrance Wt1 tm1Jae 2669009 involves: 129S4/SvJae * C57BL/6 * MF1 MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:10469569
PMID:17071579
2024-01-30 12:20:58 0
Fn1tm1Feb/Fn1tm1Feb
 
Resource Report

The record is no longer available at this source.
RRID:MGI:2668713 Mus musculus Allele Detail: Targeted This is a legacy resource. reproductive system phenotype, homeostasis/metabolism phenotype, premature death, abnormal protein level Fn1 tm1Feb 2668713 involves: 129X1/SvJ MGI, Mouse Genome Informatics MGI MGI Availability unknown check source stock center PMID:12847088 2024-01-30 12:20:58 0

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