Searching the RRID Resource Information Network
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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 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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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 | MMRRC | 2026-10-24 06:28:08 | 0 | |||
|
STOCK Tg(Angpt2-EGFP)DJ90Gsat/Mmucd Resource Report Resource Website 1+ mentions |
RRID:MMRRC_000302-UCD | Mus musculus | Research areas: Cell Biology, Developmental Biology, Neurobiology, Research Tools; Mutation Type: Transgenic ; Collection: GENSAT | Angpt2|EGFP|| | 000302-UCD | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:14586460 | MMRRC_302-UCD, MMRRC_000302, MMRRC_32 | MMRRC | 2026-10-24 06:28:05 | 2 | ||||
|
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 | MMRRC | 2026-10-24 06:28:06 | 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 | MMRRC | 2026-10-24 06:28:06 | 0 | |||
|
BayGenomics ES cell line DTM010 Resource Report Resource Website |
RRID:MMRRC_000473-UCD | Mus musculus | Research areas: ; Mutation Type: Gene Trap ; Collection: BayGenomics | Paip2 | 000473-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_473-UCD, MMRRC_000473, MMRRC_473 | MMRRC | 2026-10-24 06:28:07 | 0 | ||||
|
C3;B6-Tg(Prnp-ATN1)150Dbo/Mmmh Resource Report Resource Website 1+ mentions |
RRID:MMRRC_000398-MU | Mus musculus | Research areas: Models for Human Disease, Neurobiology, Sensorineural; Mutation Type: Transgenic ; Collection: | Prnp|Atn1| | 000398-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:10677044 | MMRRC_398-MU, MMRRC_000398, MMRRC_398 | MMRRC | 2026-10-24 06:28:06 | 2 | ||||
|
STOCK Tg(Ins1-EGFP/GH1)14Hara/Mmmh Resource Report Resource Website |
RRID:MMRRC_000438-MU | Mus musculus | Research areas: Developmental Biology, Endocrine Deficiency, Models for Human Disease, Research Tools; Mutation Type: Transgenic ; Collection: BCBC-Beta Cell Biology Consortium | GH1|EGFP|Ins1| | 000438-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12388130 | MMRRC_438-MU, MMRRC_000438, MMRRC_438 | MMRRC | 2026-10-24 06:28:06 | 0 | ||||
|
STOCK Tg(Htr5b-EGFP)BZ265Gsat/Mmmh Resource Report Resource Website 1+ mentions |
RRID:MMRRC_000300-MU | Mus musculus | Research areas: Cell Biology, Developmental Biology, Neurobiology, Research Tools; Mutation Type: Transgenic ; Collection: GENSAT | Htr5b|EGFP|| | 000300-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:14586460 | MMRRC_300-MU, MMRRC_000300, MMRRC_3 | MMRRC | 2026-10-24 06:28:05 | 1 | ||||
|
BayGenomics ES cell line DTM006 Resource Report Resource Website |
RRID:MMRRC_000469-UCD | Mus musculus | Research areas: ; Mutation Type: Gene Trap ; Collection: BayGenomics | 000469-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_469-UCD, MMRRC_000469, MMRRC_469 | MMRRC | 2026-10-24 06:28:07 | 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 | MMRRC | 2026-10-24 06:28:06 | 1 | |||
|
B6.Cg-Tyrp1b-c Tyrc-ch Dctslt/Mmmh Resource Report Resource Website |
RRID:MMRRC_000363-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | diluted coat color [MP:0000371]| mottled coat [MP:0000421]| abnormal locomotor behavior [MP:0001392]| abnormal coat appearance [MP:0001510]| female infertility [MP:0001926]| abnormal coat/hair pigmentation [MP:0002075]| premature death [MP:0002083]| absent coat pigmentation [MP:0005171]| abnormal hair follicle pheomelanosome pheomelanin content [MP:0006370]| absent eye pigmentation [MP:0008480]| diluted coat color [MP:0000371]| abnormal coat/hair pigmentation [MP:0002075] | |||Dct|Tyr|Tyrp1 | 000363-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:2118105 PMID:1537334 |
MMRRC_363-MU, MMRRC_000363, MMRRC_363 | MMRRC | 2026-10-24 06:28:08 | 0 | |||
|
STOCK Tg(Gfap-EGFP)CV94Gsat/Mmmh Resource Report Resource Website 1+ mentions |
RRID:MMRRC_000315-MU | Mus musculus | Research areas: Cell Biology, Developmental Biology, Neurobiology, Research Tools; Mutation Type: Transgenic ; Collection: GENSAT | Gfap|EGFP| | 000315-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:14586460 | MMRRC_315-MU, MMRRC_000315, MMRRC_315 | MMRRC | 2026-10-24 06:28:07 | 3 | ||||
|
BayGenomics ES cell line DTM007 Resource Report Resource Website |
RRID:MMRRC_000470-UCD | Mus musculus | Research areas: ; Mutation Type: Gene Trap ; Collection: BayGenomics | Pvt1 | 000470-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_470-UCD, MMRRC_000470, MMRRC_47 | MMRRC | 2026-10-24 06:28:09 | 0 | ||||
|
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 | MMRRC | 2026-10-24 06:28:06 | 3 | ||||
|
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 | MMRRC | 2026-10-24 06:28:08 | 0 | |||
|
STOCK Tg(Sema3e-EGFP)AY35Gsat/Mmmh Resource Report Resource Website |
RRID:MMRRC_000320-MU | Mus musculus | Research areas: Cell Biology, Developmental Biology, Neurobiology, Research Tools; Mutation Type: Transgenic ; Collection: GENSAT | Sema3e|EGFP| | 000320-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:14586460 | MMRRC_320-MU, MMRRC_000320, MMRRC_32 | MMRRC | 2026-10-24 06:28:07 | 0 | ||||
|
B6;129P2-Sphk2Gt(NPX357)Byg/Mmucd Resource Report Resource Website |
RRID:MMRRC_000402-UCD | Mus musculus | Research areas: Cell Biology; Mutation Type: Gene Trap ; Collection: BayGenomics | Sphk2 | 000402-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_402-UCD, MMRRC_000402, MMRRC_42 | MMRRC | 2026-10-24 06:28:06 | 0 | ||||
|
STOCK Tg(Pdx1-cre)89.1Dam/Mmucd Resource Report Resource Website 1+ mentions |
RRID:MMRRC_000353-UCD | Mus musculus | Research areas: Developmental Biology, Diabetes, Endocrine Deficiency; Mutation Type: Transgenic ; Collection: BCBC-Beta Cell Biology Consortium | cre|Pdx1| | 000353-UCD | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:11973276 | MMRRC_353-UCD, MMRRC_000353, MMRRC_353 | MMRRC | 2026-10-24 06:28:08 | 1 | ||||
|
B6;129P2-Pank4Gt(XB396)Byg/Mmucd Resource Report Resource Website |
RRID:MMRRC_000447-UCD | Mus musculus | Research areas: ; Mutation Type: Gene Trap ; Collection: BayGenomics | Pank4 | 000447-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_447-UCD, MMRRC_000447, MMRRC_447 | MMRRC | 2026-10-24 06:28:07 | 0 | ||||
|
FVB-Tg(ABCA1)1Hgc/Mmmh Resource Report Resource Website |
RRID:MMRRC_000385-MU | Mus musculus | Research areas: Cardiovascular, Models for Human Disease, Research Tools; Mutation Type: Transgenic ; Collection: | ABCA1 | 000385-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:11279093 | MMRRC_385-MU, MMRRC_000385, MMRRC_385 | MMRRC | 2026-10-24 06:28:06 | 0 |
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