Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Preparing word cloud

×

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.

Suggested Search Criteria

Enter extra filters to help narrow your search

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Background:targeted mutation (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

10,847 Results - per page

Show More Columns | Download Top 1000 Results

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
FVB.129S2-Plntm1Egk/Mmmh
 
Resource Report
Resource Website
RRID:MMRRC_000228-MU Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: abnormal heart shape [MP:0000277]| abnormal interventricular septum morphology [MP:0000281]| abnormal eye development [MP:0001286]| cardiac hypertrophy [MP:0001625]| abnormal cardiac output [MP:0001627]| premature death [MP:0002083]| dilated heart left ventricle [MP:0002753]| dilated cardiomyopathy [MP:0002795]| increased heart weight [MP:0002833]| thick ventricular wall [MP:0002953]| abnormal cardiac muscle contractility [MP:0002972]| abnormal locomotor activation [MP:0003313]| abnormal cardiac muscle relaxation [MP:0004084]| abnormal myocardial fiber physiology [MP:0004215]| abnormal calcium ion homeostasis [MP:0004231]| enlarged myocardial fiber [MP:0004564]| decreased cardiac muscle contractility [MP:0005140]| decreased heart rate [MP:0005333]| increased cardiac muscle contractility [MP:0005599]| congestive heart failure [MP:0006138]| atrial fibrillation [MP:0008543]| increased heart left ventricle size [MP:0010579]| abnormal heart left ventricle pressure [MP:0010754]| neonatal lethality [MP:0011087]| complete penetrance [MP:0011952]| decreased cardiac stroke volume [MP:0020346] Pln 000228-MU Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:12504816 MMRRC_228-MU, MMRRC_000228, MMRRC_228 2026-02-14 07:34:00 0
B6.129S6-Il4tm1Rao/Mmnc
 
Resource Report
Resource Website
RRID:MMRRC_000227-UNC Mus musculus Research areas: Cell Biology, Immunology and Inflammation, Models for Human Disease; Mutation Type: Targeted Mutation ; Collection: abnormal mast cell physiology [MP:0002423]| abnormal T-helper 2 physiology [MP:0005466]| decreased interleukin-13 secretion [MP:0008673]| decreased interleukin-4 secretion [MP:0008700] Il4 000227-UNC Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:12150890 MMRRC_227-UNC, MMRRC_000227, MMRRC_227 2026-02-14 07:34:00 0
B6.129-Kif5atm1Gsn/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_000223-UCD Mus musculus Research areas: Apoptosis, Cell Biology, Developmental Biology, Internal/Organ, Models for Human Disease, Neurobiology, Research Tools, Sensorineural; Mutation Type: Targeted Mutation ; Collection: tremors [MP:0000745]| hindlimb paralysis [MP:0000755]| abnormal motor neuron morphology [MP:0000937]| sporadic seizures [MP:0000951]| atelectasis [MP:0001177]| decreased body weight [MP:0001262]| decreased body size [MP:0001265]| impaired coordination [MP:0001405]| abnormal posture [MP:0001504]| cyanosis [MP:0001575]| abnormal breathing pattern [MP:0001951]| premature death [MP:0002083]| abnormal axonal transport [MP:0004768]| axon degeneration [MP:0005405]| abnormal protein level [MP:0008469]| abnormal vesicle-mediated transport [MP:0008546]| lethality at weaning [MP:0011084]| incomplete penetrance [MP:0011087] Kif5a 000223-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:12682084 MMRRC_223-UCD, MMRRC_000223, MMRRC_223 2026-02-14 07:34:00 0
B10.129-Tcrdtm1Mom/Mmnc
 
Resource Report
Resource Website
RRID:MMRRC_000334-UNC Mus musculus Research areas: Cancer, Immunology and Inflammation; Mutation Type: Targeted Mutation ; Collection: enlarged liver [MP:0000599]| enlarged spleen [MP:0000691]| spleen hypoplasia [MP:0000694]| absent CD8-positive [MP:0000727]| alpha-beta T cells [MP:0001191]| abnormal skin condition [MP:0001194]| dermatitis [MP:0001805]| decreased IgG level [MP:0001807]| decreased IgA level [MP:0001823]| thymus hypoplasia [MP:0001825]| arrested T cell differentiation [MP:0002023]| increased B cell derived lymphoma incidence [MP:0002024]| increased T cell derived lymphoma incidence [MP:0002083]| premature death [MP:0002132]| abnormal respiratory system morphology [MP:0002133]| abnormal respiratory system physiology [MP:0002407]| abnormal double-negative T cell morphology [MP:0002492]| decreased IgE level [MP:0002494]| increased IgM level [MP:0002495]| increased IgA level [MP:0002796]| impaired skin barrier function [MP:0002816]| colitis [MP:0003306]| small intestinal inflammation [MP:0003725]| increased autoantibody level [MP:0003726]| decreased autoantibody level [MP:0003790]| absent CD4-positive [MP:0004762]| alpha beta T cells [MP:0004796]| increased anti-double stranded DNA antibody level [MP:0004829]| increased anti-histone antibody level [MP:0005014]| increased anti-chromatin antibody level [MP:0005015]| increased B cell number [MP:0005016]| increased T cell number [MP:0005018]| decreased lymphocyte cell number [MP:0005025]| decreased T cell number [MP:0005092]| abnormal response to infection [MP:0005617]| decreased double-positive T cell number [MP:0006042]| increased susceptibility to type IV hypersensitivity reaction [MP:0008098]| increased apoptosis [MP:0008173]| decreased plasma cell number [MP:0008181]| increased follicular B cell number [MP:0008188]| increased marginal zone B cell number [MP:0008210]| abnormal transitional stage B cell morphology [MP:0008214]| increased mature B cell number [MP:0008348]| increased immature B cell number [MP:0008356]| absent gamma-delta T cells [MP:0008495]| abnormal gamma-delta T cell differentiation [MP:0008757]| decreased IgG1 level [MP:0009925]| abnormal T cell receptor gamma chain V-J recombination [MP:0010229]| increased transitional stage T2 B cell number [MP:0010286]| increased transitional stage T3 B cell number [MP:0011320]| increased plasmacytoma incidence [MP:0011427]| abnormal glomerular capillary morphology [MP:0020519] Tcrd 000334-UNC Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:8361537 MMRRC_334-UNC, MMRRC_000334, MMRRC_334 2026-02-14 07:34:03 0
B6.Cg-Mecp2tm1.1Jae/Mmucd
 
Resource Report
Resource Website
1+ mentions
RRID:MMRRC_000415-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: tremors [MP:0000745]| decreased brain size [MP:0000774]| abnormal olfactory bulb morphology [MP:0000819]| obese [MP:0001261]| decreased body weight [MP:0001262]| decreased anxiety-related response [MP:0001364]| ataxia [MP:0001393]| hypoactivity [MP:0001402]| impaired coordination [MP:0001405]| abnormal gait [MP:0001406]| abnormal pilomotor reflex [MP:0001492]| abnormal respiration [MP:0001943]| abnormal breathing pattern [MP:0001951]| apnea [MP:0001957]| premature death [MP:0002083]| decreased brain weight [MP:0002175]| abnormal motor learning [MP:0002804]| abnormal neuron morphology [MP:0002882]| increased susceptibility to age related obesity [MP:0003212]| abnormal behavior [MP:0004924]| abnormal brain wave pattern [MP:0004994]| cachexia [MP:0005150]| lethargy [MP:0005202]| abnormal action potential [MP:0005402]| tachypnea [MP:0005426]| abnormal body temperature [MP:0005535]| abnormal hippocampus CA2 region morphology [MP:0008265]| increased liver triglyceride level [MP:0009355]| increased brain cholesterol level [MP:0010162] Mecp2 000415-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:11242118
PMID:16439027
MMRRC_415-UCD, MMRRC_000415, MMRRC_415 2026-02-14 07:34:04 6
STOCK Ptf1atm1.1(cre)Cvw/Mmnc
 
Resource Report
Resource Website
1+ mentions
RRID:MMRRC_000435-UNC Mus musculus Research areas: Diabetes, Endocrine Deficiency; Mutation Type: Targeted Mutation ; Collection: BCBC-Beta Cell Biology Consortium jaundice [MP:0000611]| enlarged spleen [MP:0000691]| paralysis [MP:0000753]| abnormal cerebellar molecular layer [MP:0000889]| weight loss [MP:0001263]| distended abdomen [MP:0001270]| increased metastatic potential [MP:0001272]| decreased metastatic potential [MP:0001273]| abnormal eye development [MP:0001286]| abnormal retina morphology [MP:0001325]| ataxia [MP:0001393]| impaired coordination [MP:0001405]| abnormal gait [MP:0001406]| abnormal motor coordination/balance [MP:0001516]| hepatic necrosis [MP:0001654]| abnormal pancreas morphology [MP:0001944]| increased tumor incidence [MP:0002020]| premature death [MP:0002083]| abnormal innervation [MP:0002184]| abnormal brain commissure morphology [MP:0002199]| abnormal inhibitory postsynaptic currents [MP:0002945]| increased retinal ganglion cell number [MP:0002983]| abnormal digestive system development [MP:0003119]| abnormal GABAergic neuron morphology [MP:0003245]| abnormal duodenum morphology [MP:0003271]| pancreas fibrosis [MP:0003334]| pancreas cysts [MP:0003336]| chronic pancreas inflammation [MP:0003341]| enlarged pancreas [MP:0003450]| abnormal nervous system morphology [MP:0003632]| absent pancreas [MP:0003655]| abnormal pancreas development [MP:0003934]| small pancreas [MP:0004247]| abnormal synaptic vesicle number [MP:0004792]| abnormal paired-pulse inhibition [MP:0004807]| abnormal thrombosis [MP:0005048]| increased susceptibility to injury [MP:0005165]| abnormal pancreatic islet morphology [MP:0005215]| abnormal amacrine cell morphology [MP:0005240]| abnormal retinal neuronal layer morphology [MP:0006069]| absent amacrine cells [MP:0006095]| absent horizontal cells [MP:0008107]| thick retinal ganglion layer [MP:0008508]| absent retinal inner plexiform layer [MP:0008514]| abnormal synaptic bouton morphology [MP:0008571]| abnormal Purkinje cell differentiation [MP:0008579]| increased pancreas weight [MP:0009108]| abnormal pancreatic duct morphology [MP:0009143]| dilated pancreatic duct [MP:0009144]| abnormal pancreatic acinar cell morphology [MP:0009146]| increased pancreatic ductal adenocarcinoma incidence [MP:0009151]| increased pancreatic intraepithelial neoplasia incidence [MP:0009152]| increased pancreas tumor incidence [MP:0009153]| absent pancreatic acini [MP:0009156]| dilated gallbladder [MP:0009343]| abnormal hepatic portal vein morphology [MP:0010668]| neonatal lethality [MP:0011087]| complete penetrance [MP:0011270]| decreased excitatory postsynaptic current amplitude [MP:0013184]| hemorrhagic ascites [MP:0013221] crePtf1a 000435-UNC Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:12185368 MMRRC_435-UNC, MMRRC_000435, MMRRC_435 2026-02-14 07:34:03 7
C3H.Cg-Tcrbtm1Mom/Mmnc
 
Resource Report
Resource Website
RRID:MMRRC_000341-UNC Mus musculus Research areas: Cancer, Immunology and Inflammation; Mutation Type: Targeted Mutation ; Collection: enlarged liver [MP:0000599]| enlarged spleen [MP:0000691]| spleen hypoplasia [MP:0000694]| absent CD8-positive [MP:0000727]| alpha-beta T cells [MP:0000938]| motor neuron degeneration [MP:0001219]| thick epidermis [MP:0001243]| abnormal dermal layer morphology [MP:0001263]| weight loss [MP:0001805]| decreased IgG level [MP:0001807]| decreased IgA level [MP:0001823]| thymus hypoplasia [MP:0001825]| arrested T cell differentiation [MP:0002023]| increased B cell derived lymphoma incidence [MP:0002083]| premature death [MP:0002132]| abnormal respiratory system morphology [MP:0002133]| abnormal respiratory system physiology [MP:0002144]| abnormal B cell differentiation [MP:0002492]| decreased IgE level [MP:0002494]| increased IgM level [MP:0002495]| increased IgA level [MP:0002816]| colitis [MP:0003691]| abnormal microglial cell physiology [MP:0003725]| increased autoantibody level [MP:0003726]| decreased autoantibody level [MP:0003790]| absent CD4-positive [MP:0004762]| alpha beta T cells [MP:0004796]| increased anti-double stranded DNA antibody level [MP:0004829]| increased anti-histone antibody level [MP:0004939]| increased anti-chromatin antibody level [MP:0004947]| abnormal B cell morphology [MP:0005014]| skin inflammation [MP:0005015]| increased B cell number [MP:0005016]| increased T cell number [MP:0005017]| decreased lymphocyte cell number [MP:0005018]| decreased B cell number [MP:0005025]| decreased T cell number [MP:0005092]| abnormal response to infection [MP:0008075]| decreased double-positive T cell number [MP:0008079]| decreased CD4-positive [MP:0008098]| alpha beta T cell number [MP:0008173]| decreased CD8-positive [MP:0008181]| alpha-beta T cell number [MP:0008188]| decreased plasma cell number [MP:0008210]| increased follicular B cell number [MP:0008214]| increased marginal zone B cell number [MP:0008495]| abnormal transitional stage B cell morphology [MP:0009925]| increased mature B cell number [MP:0010229]| increased immature B cell number [MP:0010286]| decreased IgG1 level [MP:0011320]| increased transitional stage T2 B cell number [MP:0011427]| increased transitional stage T3 B cell number [MP:0020519] Tcrb 000341-UNC Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:1359428
PMID:2108043
PMID:1730159
PMID:1707404
MMRRC_341-UNC, MMRRC_000341, MMRRC_341 2026-02-14 07:34:02 0
B6.129X1-Prkar1atm1Gsm/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_000413-UCD Mus musculus Research areas: Cancer, Reproduction; Mutation Type: Targeted Mutation ; Collection: abnormal cell morphology [MP:0000358]| abnormal foregut morphology [MP:0000474]| abnormal somite shape [MP:0001691]| abnormal embryo size [MP:0001697]| decreased embryo size [MP:0001698]| pericardial edema [MP:0001787]| reduced male fertility [MP:0001922]| increased tumor incidence [MP:0002020]| increased sarcoma incidence [MP:0002032]| abnormal developmental patterning [MP:0002084]| abnormal embryonic tissue morphology [MP:0002085]| abnormal primitive streak morphology [MP:0002231]| enhanced wound healing [MP:0002724]| increased hepatocellular carcinoma incidence [MP:0003331]| increased hemangiosarcoma incidence [MP:0003667]| decreased heart rate variability [MP:0003929]| embryonic growth retardation [MP:0003984]| failure of initiation of embryo turning [MP:0004180]| increased fibrosarcoma incidence [MP:0010363]| embryonic lethality during organogenesis [MP:0011098]| complete penetrance [MP:0011205]| excessive folding of visceral yolk sac [MP:0011732]| decreased somite size [MP:0012081]| absent heart tube [MP:0012183]| decreased paraxial mesoderm size [MP:0012272]| decreased axial mesoderm size [MP:0012498] Prkar1a 000413-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:12004056
PMID:15371594
MMRRC_413-UCD, MMRRC_000413, MMRRC_413 2026-02-14 07:34:03 0
129S-Prrx1tm1Jfm/Mmmh
 
Resource Report
Resource Website
1+ mentions
RRID:MMRRC_000347-MU Mus musculus Research areas: Developmental Biology; Mutation Type: Targeted Mutation ; Collection: small ears [MP:0000018]| abnormal ear position [MP:0000023]| short mandible [MP:0000088]| cleft palate [MP:0000111]| abnormal tooth development [MP:0000116]| absent incisors [MP:0000125]| abnormal cranium morphology [MP:0000438]| abnormal maxilla morphology [MP:0000455]| abnormal mandible morphology [MP:0000458]| short limbs [MP:0000547]| pulmonary hypoplasia [MP:0001178]| decreased body size [MP:0001265]| eyelids open at birth [MP:0001302]| absent eyelids [MP:0001341]| aphagia [MP:0001438]| cyanosis [MP:0001575]| abnormal respiration [MP:0001943]| respiratory distress [MP:0001954]| neonatal lethality [MP:0002058]| abnormal limb morphology [MP:0002109]| abnormal ameloblast morphology [MP:0002650]| abnormal long bone morphology [MP:0003723]| abnormal lung vasculature morphology [MP:0004007]| growth retardation of incisors [MP:0005359]| abnormal Meckel's cartilage morphology [MP:0005587]| neonatal lethality [MP:0011087] Prrx1 000347-MU Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:9876178 MMRRC_347-MU, MMRRC_000347, MMRRC_347 2026-02-14 07:34:03 2
B6;129-Hgftm1Jmw/Mmnc
 
Resource Report
Resource Website
1+ mentions
RRID:MMRRC_000423-UNC Mus musculus Research areas: Apoptosis, Cancer, Cell Biology, Developmental Biology, Internal/Organ, Metabolism, Models for Human Disease, Research Tools; Mutation Type: Targeted Mutation ; Collection: decreased hepatocyte proliferation [MP:0004001] decreased liver regeneration [MP:0005517] Hgf 000423-UNC Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:15383179 MMRRC_423-UNC, MMRRC_000423, MMRRC_423 2026-02-14 07:34:04 2
STOCK Pdx1tm4Cvw/Mmnc
 
Resource Report
Resource Website
RRID:MMRRC_000440-UNC Mus musculus Research areas: Developmental Biology, Diabetes, Endocrine Deficiency, Research Tools; Mutation Type: Targeted Mutation ; Collection: BCBC-Beta Cell Biology Consortium abnormal pancreas morphology [MP:0001944]| no abnormal phenotype detected [MP:0002169]| decreased circulating insulin level [MP:0002727]| decreased pancreatic beta cell number [MP:0003339]| impaired glucose tolerance [MP:0005293]| increased circulating glucose level [MP:0005559]| increased pancreatic alpha cell number [MP:0009176]| increased pancreatic delta cell number [MP:0009180]| disorganized pancreatic islets [MP:0009254]| decreased pancreatic beta cell proliferation [MP:0011820]| increased pancreatic alpha cell proliferation [MP:0014109] Pdx1 000440-UNC Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC MMRRC_440-UNC, MMRRC_000440, MMRRC_44 2026-02-14 07:34:03 0
C3N.129P2(B6)-Tcrdtm1Mom/Mmnc
 
Resource Report
Resource Website
RRID:MMRRC_000342-UNC Mus musculus Research areas: Cancer, Immunology and Inflammation; Mutation Type: Targeted Mutation ; Collection: enlarged liver [MP:0000599]| enlarged spleen [MP:0000691]| spleen hypoplasia [MP:0000694]| absent CD8-positive [MP:0000727]| alpha-beta T cells [MP:0001191]| abnormal skin condition [MP:0001194]| dermatitis [MP:0001805]| decreased IgG level [MP:0001807]| decreased IgA level [MP:0001823]| thymus hypoplasia [MP:0001825]| arrested T cell differentiation [MP:0002023]| increased B cell derived lymphoma incidence [MP:0002024]| increased T cell derived lymphoma incidence [MP:0002083]| premature death [MP:0002132]| abnormal respiratory system morphology [MP:0002133]| abnormal respiratory system physiology [MP:0002407]| abnormal double-negative T cell morphology [MP:0002492]| decreased IgE level [MP:0002494]| increased IgM level [MP:0002495]| increased IgA level [MP:0002796]| impaired skin barrier function [MP:0002816]| colitis [MP:0003306]| small intestinal inflammation [MP:0003725]| increased autoantibody level [MP:0003726]| decreased autoantibody level [MP:0003790]| absent CD4-positive [MP:0004762]| alpha beta T cells [MP:0004796]| increased anti-double stranded DNA antibody level [MP:0004829]| increased anti-histone antibody level [MP:0005014]| increased anti-chromatin antibody level [MP:0005015]| increased B cell number [MP:0005016]| increased T cell number [MP:0005018]| decreased lymphocyte cell number [MP:0005025]| decreased T cell number [MP:0005092]| abnormal response to infection [MP:0005617]| decreased double-positive T cell number [MP:0006042]| increased susceptibility to type IV hypersensitivity reaction [MP:0008098]| increased apoptosis [MP:0008173]| decreased plasma cell number [MP:0008181]| increased follicular B cell number [MP:0008188]| increased marginal zone B cell number [MP:0008210]| abnormal transitional stage B cell morphology [MP:0008214]| increased mature B cell number [MP:0008348]| increased immature B cell number [MP:0008356]| absent gamma-delta T cells [MP:0008495]| abnormal gamma-delta T cell differentiation [MP:0008757]| decreased IgG1 level [MP:0009925]| abnormal T cell receptor gamma chain V-J recombination [MP:0010229]| increased transitional stage T2 B cell number [MP:0010286]| increased transitional stage T3 B cell number [MP:0011320]| increased plasmacytoma incidence [MP:0011427]| abnormal glomerular capillary morphology [MP:0020519] Tcrd 000342-UNC Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:8361537 MMRRC_342-UNC, MMRRC_000342, MMRRC_342 2026-02-14 07:34:03 0
B6;129S4-Neurod1tm1Jle/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_000367-UCD Mus musculus Research areas: Apoptosis, Cell Biology, Developmental Biology, Diabetes, Endocrine Deficiency, Models for Human Disease, Neurobiology, Sensorineural; Mutation Type: Targeted Mutation ; Collection: BCBC-Beta Cell Biology Consortium absent dentate gyrus [MP:0000814]| small cerebellum [MP:0000852]| abnormal cerebellar foliation [MP:0000857]| thin external granule cell layer [MP:0000873]| abnormal Purkinje cell morphology [MP:0000877]| decreased Purkinje cell number [MP:0000880]| abnormal cerebellar granule layer morphology [MP:0000886]| decreased sensory neuron number [MP:0000966]| abnormal sensory neuron innervation pattern [MP:0000968]| decreased body weight [MP:0001262]| decreased retinal photoreceptor cell number [MP:0001327]| abnormal optic nerve morphology [MP:0001330]| ataxia [MP:0001393]| abnormal motor coordination/balance [MP:0001516]| impaired balance [MP:0001525]| hyperglycemia [MP:0001559]| postnatal growth retardation [MP:0001732]| deafness [MP:0001967]| abnormal vestibular ganglion morphology [MP:0002856]| increased retinal ganglion cell number [MP:0002983]| absent cochlear ganglion [MP:0003146]| abnormal cochlear sensory epithelium morphology [MP:0003308]| reduced modiolus [MP:0003310]| abnormal vestibulocochlear ganglion morphology [MP:0003703]| abnormal retinal layer morphology [MP:0003727]| abnormal retinal photoreceptor layer morphology [MP:0003728]| abnormal retinal outer nuclear layer morphology [MP:0003731]| abnormal retinal inner nuclear layer morphology [MP:0003733]| absent endocochlear potential [MP:0004410]| abnormal amacrine cell morphology [MP:0005240]| abnormal retinal ganglion layer morphology [MP:0005241]| abnormal Muller cell morphology [MP:0005547]| abnormal horizontal cell morphology [MP:0006068]| abnormal retinal neuronal layer morphology [MP:0006069]| abnormal retinal apoptosis [MP:0006072]| abnormal retinal bipolar cell morphology [MP:0006073]| absent amacrine cells [MP:0006095]| decreased retinal ganglion cell number [MP:0006309]| decreased amacrine cell number [MP:0008106]| decreased retinal cone cell number [MP:0008446]| thin retinal inner nuclear layer [MP:0008511]| disorganized retinal outer nuclear layer [MP:0008516]| abnormal neuron differentiation [MP:0009937]| postnatal lethality [MP:0011085]| complete penetrance [MP:0011089]| perinatal lethality [MP:0030005] Neurod1 000367-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:10398678
PMID:11152640
MMRRC_367-UCD, MMRRC_000367, MMRRC_367 2026-02-14 07:34:02 0
B6.129-Sgcdtm1Kcam/Mmmh
 
Resource Report
Resource Website
1+ mentions
RRID:MMRRC_000406-MU Mus musculus Research areas: Cardiovascular, Developmental Biology, Models for Human Disease, Neurobiology; Mutation Type: Targeted Mutation ; Collection: abnormal heart morphology [MP:0000266]| dystrophic muscle [MP:0000752]| abnormal cardiovascular system physiology [MP:0001544]| premature death [MP:0002083]| dilated cardiomyopathy [MP:0002795]| dystrophic cardiac calcinosis [MP:0002837]| coronary artery stenosis [MP:0003024]| cardiac fibrosis [MP:0003141]| skeletal muscle necrosis [MP:0003852]| abnormal heart ventricle morphology [MP:0005294]| cardiomyopathy [MP:0005330]| myocardial necrosis [MP:0006085]| increased sensitivity to induced morbidity/mortality [MP:0009763]| decreased QRS amplitude [MP:0010394] Sgcd 000406-MU Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:10481911
PMID:11160141
MMRRC_406-MU, MMRRC_000406, MMRRC_46 2026-02-14 07:34:03 1
B6.129-Eya1tm1Rilm/Mmucd
 
Resource Report
Resource Website
RRID:MMRRC_000361-UCD Mus musculus Research areas: Developmental Biology; Mutation Type: Targeted Mutation ; Collection: abnormal inner ear morphology [MP:0000026]| abnormal cochlea morphology [MP:0000031]| abnormal lateral semicircular canal morphology [MP:0000037]| absent endolymphatic duct [MP:0000041]| absent premaxilla [MP:0000090]| abnormal basisphenoid bone morphology [MP:0000106]| rib fusion [MP:0000154]| double outlet right ventricle [MP:0000284]| decreased cell proliferation [MP:0000352]| microcephaly [MP:0000433]| abnormal cranium morphology [MP:0000438]| abnormal jaw morphology [MP:0000454]| mandible hypoplasia [MP:0000460]| abnormal pulmonary artery morphology [MP:0000484]| absent kidney [MP:0000520]| absent parathyroid glands [MP:0000680]| athymia [MP:0000705]| abnormal skeletal muscle morphology [MP:0000759]| abnormal facial nerve morphology [MP:0001071]| abnormal vestibulocochlear nerve morphology [MP:0001072]| abnormal geniculate ganglion morphology [MP:0001082]| absent petrosal ganglion [MP:0001086]| eyelids open at birth [MP:0001302]| abnormal thyroid cartilage morphology [MP:0002260]| abnormal semicircular canal morphology [MP:0002428]| persistent truncus arteriosis [MP:0002633]| pituitary gland hypoplasia [MP:0002659]| cochlear ganglion degeneration [MP:0002857]| abnormal posterior semicircular canal morphology [MP:0002858]| abnormal cardiovascular development [MP:0002925]| abnormal hyoid bone morphology [MP:0003056]| absent malleus processus brevis [MP:0003110]| anotia [MP:0003142]| absent cochlea [MP:0003147]| decreased cochlear coiling [MP:0003148]| absent lateral semicircular canal [MP:0003161]| decreased lateral semicircular canal size [MP:0003162]| absent posterior semicircular canal [MP:0003163]| decreased posterior semicircular canal size [MP:0003164]| decreased superior semicircular canal size [MP:0003166]| renal hypoplasia [MP:0003446]| thyroid hypoplasia [MP:0003499]| single kidney [MP:0003604]| small lung [MP:0003641]| absent ureter [MP:0003722]| fusion of middle ear ossicles [MP:0003740]| abnormal craniofacial development [MP:0003935]| abnormal aortic arch morphology [MP:0004113]| interrupted aortic arch [MP:0004157]| right aortic arch [MP:0004158]| retroesophageal right subclavian artery [MP:0004160]| absent stapes [MP:0004204]| abnormal epaxial muscle morphology [MP:0004248]| absent vestibular ganglion [MP:0004299]| small otic vesicle [MP:0004310]| absent inner ear vestibule [MP:0004314]| absent vestibular saccule [MP:0004315]| small vestibular saccule [MP:0004317]| decreased vestibular hair cell number [MP:0004328]| increased cochlear inner hair cell number [MP:0004395]| abnormal vestibular labyrinth morphology [MP:0004427]| abnormal pterygoid process morphology [MP:0004452]| abnormal pubis morphology [MP:0004506]| abnormal ischium morphology [MP:0004507]| abnormal orientation of cochlear hair cell stereociliary bundles [MP:0004522]| decreased outer hair cell stereocilia number [MP:0004529]| absent maxilla [MP:0004539]| cervical vertebral fusion [MP:0004620]| conductive hearing loss [MP:0004739]| impaired branching involved in ureteric bud morphogenesis [MP:0004936]| abnormal cell differentiation [MP:0005076]| abnormal middle ear ossicle morphology [MP:0005105]| abnormal incus morphology [MP:0005106]| abnormal stapes morphology [MP:0005107]| abnormal extraocular muscle morphology [MP:0005247]| abnormal zygomatic bone morphology [MP:0005270]| abnormal temporal bone morphology [MP:0005272]| small cranium [MP:0005352]| small pituitary gland [MP:0005361]| absent outer ear [MP:0005579]| abnormal endolymphatic duct morphology [MP:0006011]| abnormal tympanic membrane morphology [MP:0006018]| decreased tympanic ring size [MP:0006020]| abnormal otic vesicle development [MP:0006030]| abnormal ureteric bud morphology [MP:0006032]| abnormal external auditory canal morphology [MP:0006033]| increased apoptosis [MP:0006042]| abnormal vestibular saccule morphology [MP:0006089]| abnormal utricle morphology [MP:0006090]| abnormal cardiac outflow tract development [MP:0006126]| absent hypaxial muscle [MP:0006284]| absent inner ear [MP:0006285]| abnormal lung epithelium morphology [MP:0006382]| increased otic epithelial cell apoptosis [MP:0008063]| decreased otic epithelial cell proliferation [MP:0008064]| short endolymphatic duct [MP:0008065]| abnormal sternocostal joint morphology [MP:0008148]| abnormal semicircular canal ampulla morphology [MP:0008488]| abnormal palate development [MP:0009653]| absent external auditory canal [MP:0009707]| abnormal mitotic spindle morphology [MP:0009760]| cleft secondary palate [MP:0009890]| decreased palatine bone horizontal plate size [MP:0009895]| decreased maxillary shelf size [MP:0009897]| abnormal hyoid bone lesser horn morphology [MP:0009914]| vascular ring [MP:0010466]| absent ureteric bud [MP:0010978]| neonatal lethality [MP:0011087]| complete penetrance [MP:0011386]| increased metanephric mesenchyme apoptosis [MP:0011967]| increased or absent threshold for auditory brainstem response [MP:0012729]| abnormal common carotid artery morphology [MP:0013163]| absent thyroid gland isthmus [MP:0013222]| abnormal first pharyngeal pouch morphology [MP:0013290]| persistent ultimobranchial bodies [MP:0030097]| preauricular pit [MP:0030155]| absent tympanic cavity [MP:0030161]| absent auditory bulla [MP:0030204]| large nasal septum [MP:0030421]| tongue muscle hypoplasia [MP:0030426] Eya1 000361-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:10471511 MMRRC_361-UCD, MMRRC_000361, MMRRC_361 2026-02-14 07:34:03 0
B6.129S6-Acadltm1Uab/Mmmh
 
Resource Report
Resource Website
RRID:MMRRC_000352-MU Mus musculus Research areas: Cardiovascular, Diabetes, Metabolism, Models for Human Disease, Reproduction; Mutation Type: Targeted Mutation ; Collection: hypoglycemia [MP:0000189]| abnormal heart morphology [MP:0000266]| increased circulating free fatty acid level [MP:0001554]| decreased litter size [MP:0001935]| postnatal lethality [MP:0002082]| premature death [MP:0002083]| abnormal lipid homeostasis [MP:0002118]| hepatic steatosis [MP:0002628]| cardiac fibrosis [MP:0003141]| increased circulating carnitine level [MP:0003979]| abnormal bile composition [MP:0004773]| increased fatty acid level [MP:0005281]| increased unsaturated fatty acid level [MP:0005283]| abnormal enzyme/coenzyme activity [MP:0005584]| lipidosis [MP:0008570]| aciduria [MP:0010028]| abnormal adaptive thermogenesis [MP:0011019]| prenatal lethality [MP:0011101] Acadl 000352-MU Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:9861014
PMID:9802886
PMID:11590124
MMRRC_352-MU, MMRRC_000352, MMRRC_352 2026-02-14 07:34:02 0
B6.129S7-Chrna5tm1Mdb/Mmnc
 
Resource Report
Resource Website
RRID:MMRRC_000421-UNC Mus musculus Research areas: Cardiovascular, Neurobiology, Research Tools; Mutation Type: Targeted Mutation ; Collection: decreased susceptibility to pharmacologically induced seizures [MP:0002887] Chrna5 000421-UNC Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:12695534
PMID:14996991
MMRRC_421-UNC, MMRRC_000421, MMRRC_421 2026-02-14 07:34:04 0
129S-Del(17Hspa1b-Hsp1a)1Dix/Mmucd
 
Resource Report
Resource Website
1+ mentions
RRID:MMRRC_000372-UCD Mus musculus Research areas: Apoptosis, Cancer, Cardiovascular, Cell Biology, Developmental Biology, Immunology and Inflammation, Models for Human Disease, Neurobiology, Reproduction; Mutation Type: Targeted Mutation ; Collection: decreased cell proliferation [MP:0000352]| increased cellular sensitivity to gamma-irradiation [MP:0002007]| increased myocardial infarction size [MP:0003037]| neurofibrillary tangles [MP:0003214]| spontaneous chromosome breakage [MP:0004029]| induced chromosome breakage [MP:0004030]| abnormal cell cycle checkpoint function [MP:0004045]| tau protein deposits [MP:0004250]| decreased mitotic index [MP:0004759]| abnormal enzyme/coenzyme activity [MP:0005584]| abnormal cell physiology [MP:0005621]| abnormal spermatocyte morphology [MP:0006379]| early cellular replicative senescence [MP:0008008]| abnormal DNA repair [MP:0008058]| decreased birth weight [MP:0009674] |Hspa1a|Hspa1b 000372-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:12714332
PMID:14678980
MMRRC_372-UCD, MMRRC_000372, MMRRC_372 2026-02-14 07:34:03 1
B6.129X1-Ntrk3tm1(cre)Lfr/Mmucd
 
Resource Report
Resource Website
1+ mentions
RRID:MMRRC_000364-UCD Mus musculus Research areas: ; Mutation Type: Targeted Mutation ; Collection: creNtrk3 000364-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:15558783 MMRRC_364-UCD, MMRRC_000364, MMRRC_364 2026-02-14 07:34:02 3
KOMP ES cell line Rtn3tm1a(KOMP)Wtsi
 
Resource Report
Resource Website
RRID:MMRRC_061692-UCD Mus musculus |Rtn3| 061692-UCD Targeted Mutation Mutant Mouse Resource and Research Center (MMRRC) MMRRC PMID:21677750 MMRRC_61692-UCD, MMRRC_061692, MMRRC_61692 2026-02-14 07:51:49 0

Can't find your Organism?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. If you want to find a specific organism, it's easier to enter an RRID or a Catalog Number to search. You can refine the search results using Facets on the left side of the search results page. If you are on the table view, you can also search in a specific column by clicking the column title and enter the keywords.

If you still could not find your organism in the search results, please help us by registering it into the system — it's easy. Organisms identifiers are registered through multiple sources depending on the species:

Can't find the RRID you're searching for? X
X
  1. RRID Portal Resources

    Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that RRID has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on RRID then you can log in from here to get additional features in RRID such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.