Searching the RRID Resource Information Network
Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
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 | 2026-09-05 04:02:16 | 0 | ||||
|
FVB/NTac-Nup210lTg(Gt(ROSA)26Sor-EGFP)130910Eps/Mmmh Resource Report Resource Website |
RRID:MMRRC_000366-MU | Mus musculus | Research areas: Cell Biology, Neurobiology, Reproduction, Research Tools; Mutation Type: Transgenic ; Collection: | EGFP||Nup210l|Gt(ROSA)26Sor | 000366-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:10491262 PMID:20034429 |
MMRRC_366-MU, MMRRC_000366, MMRRC_366 | 2026-09-05 04:02:15 | 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 | 2026-09-05 04:02:15 | 0 | |||
|
STOCK Tg(Cdkn2d-EGFP)DZ41Gsat/Mmucd Resource Report Resource Website |
RRID:MMRRC_000322-UCD | Mus musculus | Research areas: Cell Biology, Developmental Biology, Neurobiology, Research Tools; Mutation Type: Transgenic ; Collection: GENSAT | Cdkn2d|EGFP|| | 000322-UCD | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:14586460 | MMRRC_322-UCD, MMRRC_000322, MMRRC_322 | 2026-09-05 04:02:15 | 0 | ||||
|
BayGenomics ES cell line DTM017 Resource Report Resource Website |
RRID:MMRRC_000480-UCD | Mus musculus | Research areas: ; Mutation Type: Gene Trap ; Collection: BayGenomics | Ptbp2 | 000480-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_480-UCD, MMRRC_000480, MMRRC_48 | 2026-09-05 04:02:16 | 0 | ||||
|
B6;129P2-IppkGt(XA232)Byg/Mmucd Resource Report Resource Website |
RRID:MMRRC_000446-UCD | Mus musculus | Research areas: ; Mutation Type: Gene Trap ; Collection: BayGenomics | embryonic lethality between somite formation and embryo turning [MP:0011097] | Ippk | 000446-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_446-UCD, MMRRC_000446, MMRRC_446 | 2026-09-05 04:02:16 | 0 | |||
|
B6;129P2-Sall4Gt(XE027)Byg/Mmucd Resource Report Resource Website |
RRID:MMRRC_000405-UCD | Mus musculus | Research areas: Developmental Biology; Mutation Type: Gene Trap ; Collection: BayGenomics | abnormal heart development [MP:0000267]| abnormal mitral valve morphology [MP:0000286]| abnormal forelimb morphology [MP:0000550]| abnormal carpal bone morphology [MP:0000554]| embryonic growth arrest [MP:0001730]| abnormal digit morphology [MP:0002110]| disorganized myocardium [MP:0002190]| thin myocardium [MP:0002652]| abnormal atrioventricular valve morphology [MP:0002745]| abnormal interventricular groove morphology [MP:0004032]| elongated metacarpal bones [MP:0004638]| abnormal phalanx morphology [MP:0005306]| embryonic lethality during organogenesis [MP:0006207]| common atrium [MP:0010406]| perimembraneous ventricular septal defect [MP:0010418]| muscular ventricular septal defect [MP:0010420]| common ventricle [MP:0010432]| embryonic lethality between implantation and somite formation [MP:0011096]| complete penetrance [MP:0011101]| prenatal lethality [MP:0011108]| incomplete penetrance [MP:0013167] | Sall4 | 000405-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_405-UCD, MMRRC_000405, MMRRC_45 | 2026-09-05 04:02:15 | 0 | |||
|
B6J;C3-Avy/HsdMmmh Resource Report Resource Website 1+ mentions |
RRID:MMRRC_000375-MU | Mus musculus | Research areas: Cancer, Cell Biology, Developmental Biology, Diabetes, Metabolism, Models for Human Disease, Reproduction, Research Tools; Mutation Type: Spontaneous Mutation ; Collection: | increased brown adipose tissue amount [MP:0000005]| diluted coat color [MP:0000371]| irregular coat pigmentation [MP:0000372]| mottled coat [MP:0000421]| increased body length [MP:0001257]| obese [MP:0001261]| abnormal eye pigmentation [MP:0001324]| hyperactivity [MP:0001399]| hypoactivity [MP:0001402]| polyphagia [MP:0001433]| abnormal coat appearance [MP:0001510]| abnormal coat/hair pigmentation [MP:0002075]| abnormal skin pigmentation [MP:0002095]| increased liver weight [MP:0002981]| yellow coat color [MP:0003136]| decreased eye pigmentation [MP:0005172]| abnormal tail pigmentation [MP:0005174]| darkened coat color [MP:0005409]| increased susceptibility to weight gain [MP:0005455]| increased percent body fat/body weight [MP:0005458]| increased circulating leptin level [MP:0005669]| abnormal hair follicle pheomelanosome pheomelanin content [MP:0006370]| abnormal ventral coat pigmentation [MP:0008237]| abnormal dorsoventral coat patterning [MP:0008238]| increased gonadal fat pad weight [MP:0009285]| increased inguinal fat pad weight [MP:0009292]| increased retroperitoneal fat pad weight [MP:0009304]| decreased tail pigmentation [MP:0011277]| decreased ear pigmentation [MP:0011279]| variegated eye pigmentation pattern [MP:0011551]| increased food intake [MP:0011939]| mottled coat [MP:0000421]| obese [MP:0001261]| increased tumor incidence [MP:0002020]| abnormal coat/hair pigmentation [MP:0002075]| genetic imprinting [MP:0003121]| yellow coat color [MP:0003136]| variegated coat color [MP:0005366]| abnormal epigenetic regulation of gene expression [MP:0012167] | |a||a | 000375-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12163699 PMID:11015573 PMID:10352119 |
MMRRC_375-MU, MMRRC_000375, MMRRC_375 | 2026-09-05 04:02:15 | 1 | |||
|
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 | 2026-09-05 04:02:15 | 0 | |||
|
STOCK Tg(Ptx3-EGFP)DO48Gsat/Mmucd Resource Report Resource Website |
RRID:MMRRC_000324-UCD | Mus musculus | Research areas: Cell Biology, Developmental Biology, Neurobiology, Research Tools; Mutation Type: Transgenic ; Collection: GENSAT | Ptx3|EGFP|| | 000324-UCD | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:14586460 | MMRRC_324-UCD, MMRRC_000324, MMRRC_324 | 2026-09-05 04:02:15 | 0 | ||||
|
STOCK Tg(Ank2-EGFP)DY49Gsat/Mmucd Resource Report Resource Website |
RRID:MMRRC_000325-UCD | Mus musculus | Research areas: Cell Biology, Developmental Biology, Neurobiology, Research Tools; Mutation Type: Transgenic ; Collection: GENSAT | Ank2|EGFP|| | 000325-UCD | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:14586460 | MMRRC_325-UCD, MMRRC_000325, MMRRC_325 | 2026-09-05 04:02:15 | 0 | ||||
|
STOCK Tg(Neurog3-cre)1Dam/Mmucd Resource Report Resource Website |
RRID:MMRRC_000351-UCD | Mus musculus | Research areas: Developmental Biology, Diabetes, Endocrine Deficiency; Mutation Type: Transgenic ; Collection: BCBC-Beta Cell Biology Consortium | cre|Neurog3| | 000351-UCD | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:11973276 | MMRRC_351-UCD, MMRRC_000351, MMRRC_351 | 2026-09-05 04:02:15 | 0 | ||||
|
B6;SJL-Tg(DBH-PTPN11)33Bmas/Mmnc Resource Report Resource Website |
RRID:MMRRC_000365-UNC | Mus musculus | Research areas: Neurobiology; Mutation Type: Transgenic ; Collection: | |PTPN11|DBH | 000365-UNC | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12482708 | MMRRC_365-UNC, MMRRC_000365, MMRRC_365 | 2026-09-05 04:02:15 | 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 | 2026-09-05 04:02:15 | 1 | |||
|
BayGenomics ES cell line DTM004 Resource Report Resource Website |
RRID:MMRRC_000467-UCD | Mus musculus | Research areas: ; Mutation Type: Gene Trap ; Collection: BayGenomics | 000467-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_467-UCD, MMRRC_000467, MMRRC_467 | 2026-09-05 04:02:16 | 0 | |||||
|
BayGenomics ES cell line DTM012 Resource Report Resource Website |
RRID:MMRRC_000475-UCD | Mus musculus | Research areas: ; Mutation Type: Gene Trap ; Collection: BayGenomics | Prdm2 | 000475-UCD | Gene Trap | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12520002 | MMRRC_475-UCD, MMRRC_000475, MMRRC_475 | 2026-09-05 04:02:16 | 0 | ||||
|
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 | 2026-09-05 04:02:15 | 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 | 2026-09-05 04:02:15 | 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 | 2026-09-05 04:02:15 | 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 | 2026-09-05 04:02:16 | 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:
Welcome to the T1D Resources search. From here you can search through a compilation of resources used by T1D and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that T1D 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.
If you have an account on T1D then you can log in from here to get additional features in T1D such as Collections, Saved Searches, and managing Resources.
Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:
If you are logged into T1D you can add data records to your collections to create custom spreadsheets across multiple sources of data.
Here are the facets that you can filter the data by.
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.
