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 Itgb8tm1Lfr/Mmucd Resource Report Resource Website |
RRID:MMRRC_000194-UCD | Mus musculus | Research areas: Apoptosis, Cell Biology, Developmental Biology, Hematology, Models for Human Disease, Neurobiology; Mutation Type: Targeted Mutation ; Collection: | cleft palate [MP:0000111]| abnormal angiogenesis [MP:0000260]| failure of vascular branching [MP:0000264]| abnormal heart morphology [MP:0000266]| absent floor plate [MP:0000926]| abnormal cardiovascular system physiology [MP:0001544]| abnormal blood vessel morphology [MP:0001614]| decreased embryo size [MP:0001698]| abnormal placenta morphology [MP:0001711]| abnormal visceral yolk sac morphology [MP:0001718]| pale yolk sac [MP:0001722]| hydroencephaly [MP:0001891]| intracranial hemorrhage [MP:0001915]| intracerebral hemorrhage [MP:0001916]| abnormal extraembryonic tissue morphology [MP:0002086]| no abnormal phenotype detected [MP:0002169]| abnormal astrocyte morphology [MP:0002182]| abnormal chorioallantoic fusion [MP:0002824]| impaired basement membrane formation [MP:0003044]| abnormal vitelline vasculature morphology [MP:0003229]| abnormal placenta vasculature [MP:0003231]| abnormal radial glial cell morphology [MP:0003648]| abnormal capillary morphology [MP:0003658]| abnormal embryonic/fetal subventricular zone morphology [MP:0004274]| abnormal brain vasculature morphology [MP:0004950]| hemopericardium [MP:0005244]| abnormal heart ventricle morphology [MP:0005294]| abnormal vascular endothelial cell morphology [MP:0006055]| increased vascular endothelial cell number [MP:0006056]| abnormal placental labyrinth vasculature morphology [MP:0008803]| palatal shelves fail to meet at midline [MP:0009888]| postnatal lethality [MP:0011085]| complete penetrance [MP:0011108]| embryonic lethality during organogenesis [MP:0011380]| incomplete penetrance [MP:0011523]| enlarged brain ventricles [MP:0012501] | Itgb8 | 000194-UCD | Targeted Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12050137 | MMRRC_194-UCD, MMRRC_000194, MMRRC_194 | 2026-09-05 04:02:13 | 0 | |||
|
B6;129-Kif3ctm3Gsn/Mmucd Resource Report Resource Website |
RRID:MMRRC_000134-UCD | Mus musculus | Research areas: Cell Biology, Models for Human Disease, Neurobiology, Sensorineural; Mutation Type: Targeted Mutation ; Collection: | no abnormal phenotype detected [MP:0002169] | Kif3c | 000134-UCD | Targeted Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:11463814 | MMRRC_134-UCD, MMRRC_000134, MMRRC_134 | 2026-09-05 04:02:12 | 0 | |||
|
B6.Cg-at-Lm Tyrc-ch/Mmmh Resource Report Resource Website |
RRID:MMRRC_000157-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] | |a||Tyr | 000157-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:2567165 PMID:8125260 PMID:469221 PMID:10614578 |
MMRRC_157-MU, MMRRC_000157, MMRRC_157 | 2026-09-05 04:02:13 | 0 | |||
|
C3;B6-Zfp423nur12/Mmucd Resource Report Resource Website |
RRID:MMRRC_000106-UCD | Mus musculus | Research areas: Neurobiology; Mutation Type: chemically induced mutation ; Collection: Mutagenesis for Dev. Defects/Baylor | tremors [MP:0000745]| abnormal telencephalon morphology [MP:0000787]| abnormal hippocampus morphology [MP:0000807]| abnormal choroid plexus morphology [MP:0000820]| dilated lateral ventricles [MP:0000825]| dilated fourth ventricle [MP:0000829]| abnormal cerebellum morphology [MP:0000849]| cerebellum hypoplasia [MP:0000851]| cerebellum vermis hypoplasia [MP:0000866]| decreased body weight [MP:0001262]| ataxia [MP:0001393]| abnormal gait [MP:0001406]| absent corpus callosum [MP:0002196]| abnormal cerebellar cortex morphology [MP:0004097]| lethality at weaning [MP:0011083] | Zfp423 | 000106-UCD | chemically induced mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12955145 | MMRRC_106-UCD, MMRRC_000106, MMRRC_16 | 2026-09-05 04:02:12 | 0 | |||
|
STOCK Plntm1Egk Tg(Myh6-Pln)1Egk/Mmmh Resource Report Resource Website |
RRID:MMRRC_000066-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|Myh6|Pln| | 000066-MU | Targeted Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:9468536 PMID:10988285 |
MMRRC_66-MU, MMRRC_000066, MMRRC_66 | 2026-09-05 04:02:12 | 0 | |||
|
D2.Cg-Ay/Mmmh Resource Report Resource Website |
RRID:MMRRC_000137-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | increased brown adipose tissue amount [MP:0000005]| increased monocyte cell number [MP:0000220]| increased body length [MP:0001257]| increased body weight [MP:0001260]| obese [MP:0001261]| decreased body weight [MP:0001262]| hyperactivity [MP:0001399]| hypoactivity [MP:0001402]| abnormal eating behavior [MP:0001431]| polyphagia [MP:0001433]| increased circulating triglyceride level [MP:0001552]| hyperglycemia [MP:0001559]| increased urine glucose level [MP:0001759]| abnormal inflammatory response [MP:0001845]| decreased incidence of induced tumors [MP:0002053]| increased circulating insulin level [MP:0002079]| abnormal lipid homeostasis [MP:0002118]| abnormal kidney morphology [MP:0002135]| abnormal renal tubule morphology [MP:0002703]| dilated renal tubules [MP:0002705]| variable body spotting [MP:0002940]| increased liver weight [MP:0002981]| yellow coat color [MP:0003136]| decreased liver weight [MP:0003402]| maternal effect [MP:0003718]| abnormal hair follicle melanogenesis [MP:0004382]| decreased adiponectin level [MP:0004893]| increased circulating cholesterol level [MP:0005178]| abnormal pancreatic islet morphology [MP:0005215]| glomerulosclerosis [MP:0005264]| improved glucose tolerance [MP:0005292]| impaired glucose tolerance [MP:0005293]| abnormal renal glomerulus morphology [MP:0005325]| insulin resistance [MP:0005331]| atherosclerotic lesions [MP:0005338]| darkened coat color [MP:0005409]| abnormal food intake [MP:0005449]| increased susceptibility to weight gain [MP:0005455]| increased percent body fat/body weight [MP:0005458]| decreased circulating glucose level [MP:0005560]| increased circulating leptin level [MP:0005669]| embryonic lethality [MP:0008762]| degranulated pancreatic beta cells [MP:0009255]| increased gonadal fat pad weight [MP:0009285]| increased inguinal fat pad weight [MP:0009292]| increased retroperitoneal fat pad weight [MP:0009304]| increased total body fat amount [MP:0010024]| embryonic lethality at implantation [MP:0011093]| complete penetrance [MP:0011339]| abnormal glomerular mesangium morphology [MP:0011353]| expanded mesangial matrix [MP:0011402]| renal cast [MP:0011409]| increased renal glomerulus basement membrane thickness [MP:0011939]| increased food intake [MP:0030050] | a | 000137-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:8146154 PMID:11277491 PMID:9450927 |
MMRRC_137-MU, MMRRC_000137, MMRRC_137 | 2026-09-05 04:02:12 | 0 | |||
|
C57BL/6J-Hps5ru2/Mmmh Resource Report Resource Website |
RRID:MMRRC_000152-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | diluted coat color [MP:0000371]| abnormal eye pigmentation [MP:0001324]| abnormal choroid pigmentation [MP:0005100]| abnormal retinal pigment epithelium morphology [MP:0005201] | Hps5 | 000152-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12548288 PMID:14718540 PMID:12445206 |
MMRRC_152-MU, MMRRC_000152, MMRRC_152 | 2026-09-05 04:02:13 | 0 | |||
|
C3;B6-ww1/Mmucd Resource Report Resource Website |
RRID:MMRRC_000082-UCD | Mus musculus | Research areas: Reproduction; Mutation Type: chemically induced mutation ; Collection: Mutagenesis for Dev. Defects/Baylor | small gonad [MP:0001116]| cryptorchism [MP:0002286]| decreased circulating testosterone level [MP:0002780] | 000082-UCD | chemically induced mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12955145 | MMRRC_82-UCD, MMRRC_000082, MMRRC_82 | 2026-09-05 04:02:12 | 0 | ||||
|
B6.C3-Tyrc-a/Mmmh Resource Report Resource Website |
RRID:MMRRC_000140-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | abnormal eye pigmentation [MP:0001324] abnormal coat/hair pigmentation [MP:0002075] | Tyr | 000140-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | MMRRC_140-MU, MMRRC_000140, MMRRC_14 | 2026-09-05 04:02:13 | 0 | ||||
|
B6.KSB-fe/Mmmh Resource Report Resource Website |
RRID:MMRRC_000186-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | diluted coat color [MP:0000371]| abnormal skin condition [MP:0001191]| skin lesions [MP:0001212]| abnormal coat/hair pigmentation [MP:0002075] | 000186-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:3732403 PMID:3816991 |
MMRRC_186-MU, MMRRC_000186, MMRRC_186 | 2026-09-05 04:02:13 | 0 | ||||
|
C3;B6-crf2/Mmucd Resource Report Resource Website |
RRID:MMRRC_000112-UCD | Mus musculus | Research areas: ; Mutation Type: chemically induced mutation ; Collection: Mutagenesis for Dev. Defects/Baylor | microcephaly [MP:0000433]| flattened snout [MP:0000447]| abnormal tooth morphology [MP:0002100]| short snout [MP:0000445]| decreased body size [MP:0001265] | 000112-UCD | chemically induced mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12955145 | MMRRC_112-UCD, MMRRC_000112, MMRRC_112 | 2026-09-05 04:02:12 | 0 | ||||
|
JU.B6J-Pax3Sp/Mmmh Resource Report Resource Website |
RRID:MMRRC_000172-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | decreased cell proliferation [MP:0000352]| belly spot [MP:0000373]| kinked tail [MP:0000585]| abnormal myogenesis [MP:0000729]| abnormal muscle development [MP:0000733]| abnormal brain ventricle morphology [MP:0000822]| exencephaly [MP:0000914]| open neural tube [MP:0000929]| small embryonic telencephalon [MP:0000936]| abnormal dorsal root ganglion morphology [MP:0000961]| abnormal enteric ganglia morphology [MP:0001045]| abnormal cranial ganglia morphology [MP:0001081]| absent skin pigmentation [MP:0001189]| edema [MP:0001785]| abnormal coat/hair pigmentation [MP:0002075]| abnormal tail morphology [MP:0002111]| abnormal neural tube morphology [MP:0002151]| abnormal semicircular canal morphology [MP:0002428]| abnormal rib development [MP:0002823]| white spotting [MP:0002938]| abnormal neural crest cell migration [MP:0002950]| spina bifida [MP:0003054]| abnormal muscle precursor cell migration [MP:0003090]| decreased cochlear coiling [MP:0003148]| abnormal midbrain development [MP:0003864]| abnormal dermomyotome development [MP:0004206]| abnormal bony labyrinth [MP:0004289]| increased mitotic index [MP:0004760]| absent coat pigmentation [MP:0005171]| abnormal endolymphatic duct morphology [MP:0006011]| abnormal otic vesicle development [MP:0006030]| abnormal vestibular saccule morphology [MP:0006089]| abnormal utricle morphology [MP:0006090]| short endolymphatic duct [MP:0008065]| absent dorsal root ganglion [MP:0008460]| abnormal tail hair pigmentation [MP:0009933]| perinatal lethality [MP:0011089]| complete penetrance [MP:0011091]| prenatal lethality [MP:0011098]| complete penetrance [MP:0011099]| embryonic lethality during organogenesis [MP:0012251]| complete penetrance [MP:0012547]| lethality throughout fetal growth and development [MP:0012701]| complete penetrance [MP:0012728]| abnormal diaphragm development [MP:0030535] | Pax3 | 000172-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:8421686 PMID:12854658 |
MMRRC_172-MU, MMRRC_000172, MMRRC_172 | 2026-09-05 04:02:13 | 0 | |||
|
C57BL/6-Mitfmi-ew/Mitfmi-sp/Mmmh Resource Report Resource Website |
RRID:MMRRC_000164-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | osteopetrosis [MP:0000067]| decreased body weight [MP:0001262]| microphthalmia [MP:0001297]| delayed tooth eruption [MP:0003053]| abnormal osteoclast morphology [MP:0004982]| absent coat pigmentation [MP:0005171]| exostosis [MP:0009877]| postnatal lethality [MP:0011085]| diluted coat color [MP:0000371]| absent skin pigmentation [MP:0001189]| abnormal coat/hair pigmentation [MP:0002075]| white spotting [MP:0002938]| yellow coat color [MP:0003136]| absent coat pigmentation [MP:0005171]| decreased eye pigmentation [MP:0005172]| hypopigmentation [MP:0005408]| abnormal hair shaft melanin granule morphology [MP:0008731]| abnormal foot pigmentation [MP:0009379]| decreased tail pigmentation [MP:0011277]| decreased ear pigmentation [MP:0011279] | Mitf | 000164-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:10790403 PMID:12586714 PMID:7874168 |
MMRRC_164-MU, MMRRC_000164, MMRRC_164 | 2026-09-05 04:02:13 | 0 | |||
|
D1.Cg-Tg(Tcra172,Tcrb172)1Wcl/Mmmh Resource Report Resource Website |
RRID:MMRRC_000131-MU | Mus musculus | Research areas: Immunology and Inflammation; Mutation Type: Transgenic ; Collection: CMGCC | |Tcra-V11.1|Trbv13-2 | 000131-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:9846690 PMID:11375419 |
MMRRC_131-MU, MMRRC_000131, MMRRC_131 | 2026-09-05 04:02:12 | 0 | ||||
|
B6.C3-DctSlt-lt/Mmmh Resource Report Resource Website |
RRID:MMRRC_000150-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | diluted coat color [MP:0000371] | Dct | 000150-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:8530099 PMID:11277491 |
MMRRC_150-MU, MMRRC_000150, MMRRC_15 | 2026-09-05 04:02:13 | 0 | |||
|
B6.Cg-Tyrc-44H/Mmmh Resource Report Resource Website |
RRID:MMRRC_000139-MU | Mus musculus | Research areas: ; Mutation Type: radiation induced mutation ; Collection: Mammalian Pigmentation | abnormal eye pigmentation [MP:0001324]| abnormal coat/hair pigmentation [MP:0002075]| absent coat pigmentation [MP:0005171]| decreased eye pigmentation [MP:0005172] | Tyr | 000139-MU | radiation induced mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | MMRRC_139-MU, MMRRC_000139, MMRRC_139 | 2026-09-05 04:02:13 | 0 | ||||
|
B6;D2-Tg(Camk2a-cre)1Lfr/Mmucd Resource Report Resource Website |
RRID:MMRRC_000189-UCD | Mus musculus | Research areas: Apoptosis, Cell Biology, Developmental Biology, Models for Human Disease, Neurobiology; Mutation Type: Transgenic ; Collection: | Camk2a|cre| | 000189-UCD | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:10798407 PMID:10995833 |
MMRRC_189-UCD, MMRRC_000189, MMRRC_189 | 2026-09-05 04:02:13 | 0 | ||||
|
B6.Cg-Mitfmi-Or/Mitfmi-sp/Mmmh Resource Report Resource Website |
RRID:MMRRC_000167-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | osteopetrosis [MP:0000067]| failure of tooth eruption [MP:0000121]| abnormal long bone metaphysis morphology [MP:0000133]| diluted coat color [MP:0000371]| belly spot [MP:0000373]| anophthalmia [MP:0001293]| microphthalmia [MP:0001297]| abnormal osteoclast physiology [MP:0001541]| female infertility [MP:0001926]| premature death [MP:0002083]| head spot [MP:0002939]| abnormal long bone epiphyseal plate morphology [MP:0003055]| increased width of hypertrophic chondrocyte zone [MP:0003408]| decreased length of long bones [MP:0004686]| abnormal osteoclast morphology [MP:0004982]| increased osteoclast cell number [MP:0004984]| decreased osteoclast cell number [MP:0004985]| absent coat pigmentation [MP:0005171]| decreased eye pigmentation [MP:0005172]| eyelids fail to open [MP:0005176]| abnormal incisor morphology [MP:0005358]| osteosclerosis [MP:0005422]| abnormal epiphyseal plate morphology [MP:0006395]| increased trabecular bone connectivity density [MP:0010932]| decreased tail pigmentation [MP:0011277]| decreased ear pigmentation [MP:0011279]| diluted coat color [MP:0000371]| absent skin pigmentation [MP:0001189]| abnormal coat/hair pigmentation [MP:0002075]| white spotting [MP:0002938]| yellow coat color [MP:0003136]| absent coat pigmentation [MP:0005171]| decreased eye pigmentation [MP:0005172]| hypopigmentation [MP:0005408]| abnormal hair shaft melanin granule morphology [MP:0008731]| abnormal foot pigmentation [MP:0009379]| decreased tail pigmentation [MP:0011277]| decreased ear pigmentation [MP:0011279] | Mitf | 000167-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:7874168 PMID:10790403 PMID:12586714 |
MMRRC_167-MU, MMRRC_000167, MMRRC_167 | 2026-09-05 04:02:13 | 0 | |||
|
B6.Cg-Mc1re Adamts20bt-2H/Mmmh Resource Report Resource Website |
RRID:MMRRC_000184-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | diluted coat color [MP:0000371]| skin lesions [MP:0001212]| thick epidermis [MP:0001219]| abnormal keratinocyte apoptosis [MP:0001224]| weight loss [MP:0001263]| decreased body size [MP:0001265]| abnormal touch/ nociception [MP:0001968]| abnormal pain threshold [MP:0001970]| increased tumor incidence [MP:0002020]| abnormal skin pigmentation [MP:0002095]| belted [MP:0002671]| white spotting [MP:0002938]| yellow coat color [MP:0003136]| increased squamous cell carcinoma incidence [MP:0004207]| increased cellular sensitivity to ionizing radiation [MP:0004227]| analgesia [MP:0004270]| abnormal hair follicle melanogenesis [MP:0004382]| abnormal melanogenesis [MP:0005077]| abnormal hair follicle pheomelanosome pheomelanin content [MP:0006370]| abnormal coat/hair pigmentation [MP:0002075]| belted [MP:0002671]| white spotting [MP:0002938]| abnormal melanoblast morphology [MP:0009783]| abnormal melanoblast migration [MP:0009784]| neonatal lethality [MP:0011087] | ||Adamts20|Mc1r | 000184-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:469221 PMID:10614578 PMID:12925592 PMID:18454205 |
MMRRC_184-MU, MMRRC_000184, MMRRC_184 | 2026-09-05 04:02:13 | 0 | |||
|
C57BL/6-Edn3ls/Mmmh Resource Report Resource Website |
RRID:MMRRC_000181-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | abnormal enteric ganglia morphology [MP:0001045]| megacolon [MP:0002731]| variable body spotting [MP:0002940]| abnormal melanosome morphology [MP:0005075]| abnormal melanoblast morphology [MP:0009783]| postnatal lethality [MP:0011085] | Edn3 | 000181-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:10614578 PMID:7719019 PMID:8001160 PMID:10679935 PMID:11434563 |
MMRRC_181-MU, MMRRC_000181, MMRRC_181 | 2026-09-05 04:02:13 | 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.
