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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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  • Database:MMRRC (facet)

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60,860 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 Authority Record Last Update Mentions Count
C57BL/6N-Cenpltm1(EUCOMM)Wtsi/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_041167-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: BaSH EUCOMM Cenpl 041167-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_41167-UCD, MMRRC_041167, MMRRC_41167 MMRRC 2026-10-24 06:38:22 0
B6N.A-Mycbp2m7Bei/Mmmh
 
Resource Report
Resource Website
RRID:MMRRC_041201-MU Mus musculus Research areas: Developmental Biology, Neurobiology; Mutation Type: chemically induced mutation ; Collection: clubfoot [MP:0000576]| abnormal corpus callosum morphology [MP:0000780]| abnormal striatum morphology [MP:0004077]| abnormal ventral striatum morphology [MP:0004103]| absent brain internal capsule [MP:0008129]| absent anterior commissure [MP:0008227]| abnormal cortical ventricular zone morphology [MP:0008458]| enlarged lateral ventricles [MP:0008535] Mycbp2 041201-MU chemically induced mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:23968836 MMRRC_41201-MU, MMRRC_041201, MMRRC_4121 MMRRC 2026-10-24 06:38:23 0
B6J.B10ScSn-Dmdmdx/Mmjax
 
Resource Report
Resource Website
RRID:MMRRC_041196-JAX Mus musculus Research areas: Cardiovascular, Cell Biology, Developmental Biology, Models for Human Disease; Mutation Type: Spontaneous Mutation ; Collection: kyphosis [MP:0000160]| increased monocyte cell number [MP:0000220]| decreased neutrophil cell number [MP:0000222]| enlarged heart [MP:0000274]| abnormal myocardial fiber morphology [MP:0000278]| decreased granulocyte number [MP:0000334]| abnormal hindlimb morphology [MP:0000556]| absent CD8-positive [MP:0000727]| alpha-beta T cells [MP:0000729]| abnormal myogenesis [MP:0000733]| abnormal muscle development [MP:0000745]| tremors [MP:0000746]| weakness [MP:0000747]| muscle weakness [MP:0000748]| progressive muscle weakness [MP:0000749]| muscle degeneration [MP:0000750]| abnormal muscle regeneration [MP:0000751]| myopathy [MP:0000752]| dystrophic muscle [MP:0000759]| abnormal skeletal muscle morphology [MP:0000761]| thin diaphragm muscle [MP:0001053]| abnormal neuromuscular synapse morphology [MP:0001262]| decreased body weight [MP:0001263]| weight loss [MP:0001264]| increased body size [MP:0001265]| decreased body size [MP:0001402]| hypoactivity [MP:0001405]| impaired coordination [MP:0001406]| abnormal gait [MP:0001407]| short stride length [MP:0001504]| abnormal posture [MP:0001515]| abnormal grip strength [MP:0001732]| postnatal growth retardation [MP:0001853]| heart inflammation [MP:0001921]| reduced fertility [MP:0001923]| reduced female fertility [MP:0001951]| abnormal breathing pattern [MP:0001953]| respiratory failure [MP:0002066]| abnormal motor capabilities/coordination/movement [MP:0002083]| premature death [MP:0002106]| abnormal muscle physiology [MP:0002108]| abnormal muscle morphology [MP:0002109]| abnormal limb morphology [MP:0002269]| muscular atrophy [MP:0002279]| abnormal diaphragm morphology [MP:0002280]| abnormal intercostal muscle morphology [MP:0002795]| dilated cardiomyopathy [MP:0002833]| increased heart weight [MP:0002837]| dystrophic cardiac calcinosis [MP:0002841]| impaired skeletal muscle contractility [MP:0002899]| fatigue [MP:0002953]| thick ventricular wall [MP:0003061]| decreased aerobic running capacity [MP:0003084]| abnormal skeletal muscle fiber morphology [MP:0003105]| abnormal heart atrium morphology [MP:0003141]| cardiac fibrosis [MP:0003155]| abnormal telomere length [MP:0003157]| impaired muscle relaxation [MP:0003199]| calcified muscle [MP:0003358]| abnormal hypaxial muscle morphology [MP:0003393]| decreased cardiac output [MP:0003790]| absent CD4-positive [MP:0003833]| alpha beta T cells [MP:0003851]| decreased satellite cell number [MP:0003852]| skeletal muscle interstitial fibrosis [MP:0003884]| skeletal muscle necrosis [MP:0004036]| decreased macrophage cell number [MP:0004087]| abnormal muscle relaxation [MP:0004089]| abnormal muscle fiber morphology [MP:0004121]| dilated sarcoplasmic reticulum [MP:0004142]| abnormal sarcolemma morphology [MP:0004145]| abnormal muscle tone [MP:0004174]| abnormal muscle electrophysiology [MP:0004232]| abnormal spine curvature [MP:0004248]| decreased muscle weight [MP:0004262]| abnormal epaxial muscle morphology [MP:0004510]| abnormal physical strength [MP:0004564]| myositis [MP:0004566]| enlarged myocardial fiber [MP:0004597]| myocardial fiber degeneration [MP:0004703]| increased susceptibility to noise-induced hearing loss [MP:0004818]| abnormal vertebral column morphology [MP:0004819]| increased skeletal muscle mass [MP:0004973]| decreased skeletal muscle mass [MP:0005015]| increased regulatory T cell number [MP:0005017]| increased T cell number [MP:0005018]| decreased B cell number [MP:0005137]| decreased T cell number [MP:0005140]| increased growth hormone level [MP:0005165]| decreased cardiac muscle contractility [MP:0005294]| increased susceptibility to injury [MP:0005330]| abnormal heart ventricle morphology [MP:0005425]| cardiomyopathy [MP:0005608]| increased macrophage cell number [MP:0005620]| cardiac interstitial fibrosis [MP:0006085]| abnormal muscle contractility [MP:0008327]| myocardial necrosis [MP:0008416]| abnormal corticotroph morphology [MP:0008560]| increased somatotroph cell size [MP:0008566]| increased tumor necrosis factor secretion [MP:0008663]| increased interferon-gamma secretion [MP:0008687]| increased interleukin-12 secretion [MP:0008699]| increased interleukin-2 secretion [MP:0008705]| increased interleukin-4 secretion [MP:0008837]| increased interleukin-6 secretion [MP:0008838]| increased transforming growth factor level [MP:0008866]| decreased transforming growth factor level [MP:0008874]| chromosomal instability [MP:0009398]| decreased physiological sensitivity to xenobiotic [MP:0009399]| abnormal skeletal muscle fiber size [MP:0009400]| increased skeletal muscle fiber size [MP:0009401]| decreased skeletal muscle fiber size [MP:0009402]| increased skeletal muscle fiber diameter [MP:0009403]| decreased skeletal muscle fiber diameter [MP:0009404]| increased variability of skeletal muscle fiber size [MP:0009405]| centrally nucleated skeletal muscle fibers [MP:0009406]| increased skeletal muscle fiber number [MP:0009410]| decreased skeletal muscle fiber number [MP:0009412]| abnormal skeletal muscle satellite cell proliferation [MP:0009413]| skeletal muscle fiber degeneration [MP:0009414]| skeletal muscle fiber atrophy [MP:0009415]| skeletal muscle fiber necrosis [MP:0009416]| skeletal muscle degeneration [MP:0009417]| cardiac muscle degeneration [MP:0009419]| skeletal muscle atrophy [MP:0009420]| skeletal muscle fibrosis [MP:0009461]| skeletal muscle endomysial fibrosis [MP:0010024]| skeletal muscle hypertrophy [MP:0010053]| increased total body fat amount [MP:0010090]| decreased grip strength [MP:0010106]| increased circulating creatine kinase level [MP:0010226]| abnormal circulating pyruvate kinase level [MP:0010227]| increased quadriceps weight [MP:0010238]| decreased quadriceps weight [MP:0010239]| increased skeletal muscle weight [MP:0010252]| decreased skeletal muscle weight [MP:0010254]| anterior subcapsular cataracts [MP:0010581]| nuclear cataracts [MP:0010632]| abnormal atrium myocardial trabeculae morphology [MP:0011086]| cardiac muscle necrosis [MP:0011952]| postnatal lethality [MP:0011966]| incomplete penetrance [MP:0011967]| decreased cardiac stroke volume [MP:0012106]| abnormal auditory brainstem response waveform shape [MP:0013237]| increased or absent threshold for auditory brainstem response [MP:0013467]| impaired exercise endurance [MP:0014143]| abnormal skeletal muscle regeneration [MP:0020309]| diaphragmitis [MP:0030428] Dmd 041196-JAX Spontaneous Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:6583703 MMRRC_41196-JAX, MMRRC_041196, MMRRC_41196 MMRRC 2026-10-24 06:38:25 0
C57BL/6N-Tnikm1Anu/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_041316-UCD Mus musculus Research areas: ; Mutation Type: chemically induced mutation ; Collection: NHMRC Australian PhenomeBank no abnormal phenotype detected [MP:0002169] Tnik 041316-UCD chemically induced mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC MMRRC_41316-UCD, MMRRC_041316, MMRRC_41316 MMRRC 2026-10-24 06:38:27 0
C57BL/6N-Tnpo3m1Anu/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_041296-UCD Mus musculus Research areas: Cell Biology, Developmental Biology, Immunology and Inflammation; Mutation Type: chemically induced mutation ; Collection: NHMRC Australian PhenomeBank embryonic lethality [MP:0008762] Tnpo3 041296-UCD chemically induced mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC MMRRC_41296-UCD, MMRRC_041296, MMRRC_41296 MMRRC 2026-10-24 06:38:24 0
B6;129S-Ropn1Gt(OST21705)Lex/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_041261-UCD Mus musculus Research areas: Cancer, Reproduction; Mutation Type: Gene Trap ; Collection: reduced male fertility [MP:0001922]| male infertility [MP:0001925]| decreased litter size [MP:0001935]| asthenozoospermia [MP:0002675] Ropn1 041261-UCD Gene Trap Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:22021175 MMRRC_41261-UCD, MMRRC_041261, MMRRC_41261 MMRRC 2026-10-24 06:38:10 0
C57BL/6N-Rbp1tm2a(EUCOMM)Hmgu/BayMmucd
 
Resource Report
Resource Website
RRID:MMRRC_041235-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: BaSH EUCOMM Rbp1 041235-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_41235-UCD, MMRRC_041235, MMRRC_41235 MMRRC 2026-10-24 06:38:23 0
C57BL/6N-Srprbtm2a(EUCOMM)Hmgu/BayMmucd
 
Resource Report
Resource Website
RRID:MMRRC_041245-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: BaSH EUCOMM Srprb 041245-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_41245-UCD, MMRRC_041245, MMRRC_41245 MMRRC 2026-10-24 06:38:09 0
C57BL/6N-Trim59tm1a(EUCOMM)Hmgu/BayMmucd
 
Resource Report
Resource Website
RRID:MMRRC_041253-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: BaSH EUCOMM Trim59 041253-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_41253-UCD, MMRRC_041253, MMRRC_41253 MMRRC 2026-10-24 06:38:09 0
C57BL/6JAnu-Hmbsm1Anu/AnuApbMmucd
 
Resource Report
Resource Website
RRID:MMRRC_041271-UCD Mus musculus Research areas: Immunology and Inflammation; Mutation Type: chemically induced mutation ; Collection: NHMRC Australian PhenomeBank Hmbs 041271-UCD chemically induced mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC MMRRC_41271-UCD, MMRRC_041271, MMRRC_41271 MMRRC 2026-10-24 06:38:24 0
B6(CBA)-Zbtb16pnky/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_041288-UCD Mus musculus Research areas: Developmental Biology; Mutation Type: chemically induced mutation ; Collection: NHMRC Australian PhenomeBank abnormal hindlimb morphology [MP:0000556]| polydactyly [MP:0000562]| reduced male fertility [MP:0001922] Zbtb16 041288-UCD chemically induced mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:10835630 MMRRC_41288-UCD, MMRRC_041288, MMRRC_41288 MMRRC 2026-10-24 06:38:24 0
C57BL/6N-Wscd1tm1a(EUCOMM)Hmgu/BayMmucd
 
Resource Report
Resource Website
RRID:MMRRC_041255-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: BaSH EUCOMM Wscd1 041255-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_41255-UCD, MMRRC_041255, MMRRC_41255 MMRRC 2026-10-24 06:38:10 0
C57BL/6N-Rpl7l1tm2a(EUCOMM)Hmgu/BayMmucd
 
Resource Report
Resource Website
RRID:MMRRC_041237-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: BaSH EUCOMM Rpl7l1 041237-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_41237-UCD, MMRRC_041237, MMRRC_41237 MMRRC 2026-10-24 06:38:09 0
C57BL/6N-Slc7a8tm2a(EUCOMM)Hmgu/BayMmucd
 
Resource Report
Resource Website
1+ mentions
RRID:MMRRC_041243-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: BaSH EUCOMM Slc7a8 041243-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_41243-UCD, MMRRC_041243, MMRRC_41243 MMRRC 2026-10-24 06:38:09 1
C57BL/6J-Tlx3m1Anu/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_041266-UCD Mus musculus Research areas: Developmental Biology, Neurobiology; Mutation Type: chemically induced mutation ; Collection: NHMRC Australian PhenomeBank impaired coordination [MP:0001405] Tlx3 041266-UCD chemically induced mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC MMRRC_41266-UCD, MMRRC_041266, MMRRC_41266 MMRRC 2026-10-24 06:38:26 0
C57BL/6N-Tra2atm2a(EUCOMM)Hmgu/BayMmucd
 
Resource Report
Resource Website
RRID:MMRRC_041251-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: BaSH EUCOMM Tra2a 041251-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_41251-UCD, MMRRC_041251, MMRRC_41251 MMRRC 2026-10-24 06:38:09 0
B6;CBA-Clcn1m1Anu/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_041264-UCD Mus musculus Research areas: Neurobiology; Mutation Type: chemically induced mutation ; Collection: NHMRC Australian PhenomeBank ataxia [MP:0001393]| abnormal gait [MP:0001406]| abnormal sensory capabilities/reflexes/nociception [MP:0002067]| muscle hypertonia [MP:0004143]| paraparesis [MP:0009434] Clcn1 041264-UCD chemically induced mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC MMRRC_41264-UCD, MMRRC_041264, MMRRC_41264 MMRRC 2026-10-24 06:38:09 0
C57BL/6N-Btkm2Anu/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_041294-UCD Mus musculus Research areas: Cell Biology, Hematology, Immunology and Inflammation; Mutation Type: chemically induced mutation ; Collection: NHMRC Australian PhenomeBank increased IgM level [MP:0002494] increased immature B cell number [MP:0008214] Btk 041294-UCD chemically induced mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC MMRRC_41294-UCD, MMRRC_041294, MMRRC_41294 MMRRC 2026-10-24 06:38:26 0
C57BL/6J-Fcer2am1AnuAnuApb
 
Resource Report
Resource Website
RRID:MMRRC_041277-UCD Mus musculus Research areas: Immunology and Inflammation; Mutation Type: chemically induced mutation ; Collection: NHMRC Australian PhenomeBank Fcer2a 041277-UCD chemically induced mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC MMRRC_41277-UCD, MMRRC_041277, MMRRC_41277 MMRRC 2026-10-24 06:38:26 0
C57BL/6N-Rbm34tm1a(EUCOMM)Hmgu/BayMmucd
 
Resource Report
Resource Website
RRID:MMRRC_041234-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: BaSH EUCOMM Rbm34 041234-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_41234-UCD, MMRRC_041234, MMRRC_41234 MMRRC 2026-10-24 06:38:26 0

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