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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.
| Organism Name | Proper Citation | Species | Synonyms |
Notes |
Phenotype | Affected Gene | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
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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