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.Cg-Tyrc-ch/Mmmh Resource Report Resource Website |
RRID:MMRRC_000144-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] | Tyr | 000144-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:6793688 PMID:3091449 |
MMRRC_144-MU, MMRRC_000144, MMRRC_144 | MMRRC | 2026-10-24 06:28:03 | 0 | |||
|
C3;B6-skc1/Mmucd Resource Report Resource Website |
RRID:MMRRC_000107-UCD | Mus musculus | Research areas: ; Mutation Type: chemically induced mutation ; Collection: Mutagenesis for Dev. Defects/Baylor | greasy coat [MP:0003849] | 000107-UCD | chemically induced mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12955145 | MMRRC_107-UCD, MMRRC_000107, MMRRC_17 | MMRRC | 2026-10-24 06:28:03 | 0 | ||||
|
FVB/N-Tg(Myh7-Pln)2Egk/Mmmh Resource Report Resource Website 1+ mentions |
RRID:MMRRC_000067-MU | Mus musculus | Research areas: ; Mutation Type: Transgenic ; Collection: | Pln|Myh7| | 000067-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:15059971 | MMRRC_67-MU, MMRRC_000067, MMRRC_67 | MMRRC | 2026-10-24 06:28:02 | 3 | ||||
|
B6J(Cg)-Adamts20bt-2H/Mmmh Resource Report Resource Website |
RRID:MMRRC_000183-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | 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 | 000183-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:10614578 PMID:12925592 PMID:18454205 |
MMRRC_183-MU, MMRRC_000183, MMRRC_183 | MMRRC | 2026-10-24 06:28:04 | 0 | |||
|
B6.Cg-MitfMi-b/Mitfmi-sp/Mmmh Resource Report Resource Website |
RRID:MMRRC_000168-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | diluted coat color [MP:0000371]| abnormal eye pigmentation [MP:0001324]| abnormal retina morphology [MP:0001325]| retinal degeneration [MP:0001326]| abnormal coat/hair pigmentation [MP:0002075]| variable body spotting [MP:0002940]| abnormal Harderian gland pigmentation [MP:0003798]| abnormal choroid pigmentation [MP:0005100]| absent coat pigmentation [MP:0005171]| decreased eye pigmentation [MP:0005172]| abnormal retinal pigment epithelium morphology [MP:0005201]| abnormal eye physiology [MP:0005253]| decreased tail pigmentation [MP:0011277]| decreased ear pigmentation [MP:0011279]| abnormal ciliary process morphology [MP:0014164]| 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 | 000168-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:10790403 PMID:12586714 PMID:8947051 |
MMRRC_168-MU, MMRRC_000168, MMRRC_168 | MMRRC | 2026-10-24 06:28:03 | 0 | |||
|
D2.C3-Tg(Myh6-Ngfb)4Fed/Mmmh Resource Report Resource Website |
RRID:MMRRC_000121-MU | Mus musculus | Research areas: ; Mutation Type: Transgenic ; Collection: | Ngf|Myh6| | 000121-MU | Transgenic | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:7750647 | MMRRC_121-MU, MMRRC_000121, MMRRC_121 | MMRRC | 2026-10-24 06:28:03 | 0 | ||||
|
B6.Cg-Mitfmi-rw/Mitfmi-sp/Mmmh Resource Report Resource Website |
RRID:MMRRC_000163-MU | Mus musculus | Research areas: ; Mutation Type: Spontaneous Mutation ; Collection: Mammalian Pigmentation | 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]| microphthalmia [MP:0001297]| abnormal eye pigmentation [MP:0001324]| abnormal coat/hair pigmentation [MP:0002075]| abnormal eye size [MP:0002697]| decreased eye pigmentation [MP:0005172] | Mitf | 000163-MU | Spontaneous Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:12586714 PMID:7874168 |
MMRRC_163-MU, MMRRC_000163, MMRRC_163 | MMRRC | 2026-10-24 06:28:03 | 0 | |||
|
C.129S2(B6)-Tgfb1tm1Doe/Mmnc Resource Report Resource Website |
RRID:MMRRC_000118-UNC | Mus musculus | Research areas: Immunology and Inflammation, Models for Human Disease; Mutation Type: Targeted Mutation ; Collection: | increased leukocyte cell number [MP:0000218]| increased cell proliferation [MP:0000351]| small spleen [MP:0000692]| enlarged lymph nodes [MP:0000702]| small seminiferous tubules [MP:0001153]| abnormal spermatogenesis [MP:0001156]| decreased body weight [MP:0001262]| decreased body size [MP:0001265]| reduced male mating frequency [MP:0001380]| hunched posture [MP:0001505]| disheveled coat [MP:0001511]| gastric necrosis [MP:0001653]| hepatic necrosis [MP:0001654]| multifocal hepatic necrosis [MP:0001655]| thymus hypoplasia [MP:0001823]| abnormal inflammatory response [MP:0001845]| brain inflammation [MP:0001847]| eye inflammation [MP:0001851]| conjunctivitis [MP:0001852]| heart inflammation [MP:0001853]| liver inflammation [MP:0001860]| lung inflammation [MP:0001861]| pancreas inflammation [MP:0001869]| salivary gland inflammation [MP:0001870]| stomach inflammation [MP:0001873]| decreased inflammatory response [MP:0001876]| male infertility [MP:0001925]| premature death [MP:0002083]| abnormal diaphragm morphology [MP:0002279]| abnormal Peyer's patch germinal center morphology [MP:0002391]| abnormal T cell physiology [MP:0002444]| oligozoospermia [MP:0002687]| decreased circulating luteinizing hormone level [MP:0002773]| decreased circulating testosterone level [MP:0002780]| abnormal testes secretion [MP:0002782]| decreased circulating follicle stimulating hormone level [MP:0002790]| increased circulating alanine transaminase level [MP:0002941]| gastric ulcer [MP:0003282]| increased susceptibility to kidney reperfusion injury [MP:0004041]| renal tubular necrosis [MP:0004154]| myositis [MP:0004510]| skin inflammation [MP:0004947]| decreased spleen weight [MP:0004953]| cachexia [MP:0005150]| increased circulating creatinine level [MP:0005553]| increased lung weight [MP:0005630]| myocardial necrosis [MP:0006085]| abnormal spermatid morphology [MP:0006380]| increased CD4-positive [MP:0008074]| alpha beta T cell number [MP:0008075]| decreased CD4-positive [MP:0008086]| alpha beta T cell number [MP:0008133]| increased T-helper 1 cell number [MP:0008566]| decreased Peyer's patch number [MP:0008872]| increased interferon-gamma secretion [MP:0008880]| abnormal physiological response to xenobiotic [MP:0009305]| lacrimal gland inflammation [MP:0009697]| decreased retroperitoneal fat pad weight [MP:0009856]| abnormal copulation [MP:0011083]| failure of ejaculation [MP:0011085]| lethality at weaning [MP:0011086]| complete penetrance [MP:0011101]| postnatal lethality [MP:0013467] | Tgfb1 | 000118-UNC | Targeted Mutation | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:11342667 | MMRRC_118-UNC, MMRRC_000118, MMRRC_118 | MMRRC | 2026-10-24 06:28:04 | 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 | MMRRC | 2026-10-24 06:28:03 | 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 | MMRRC | 2026-10-24 06:28:04 | 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 | MMRRC | 2026-10-24 06:28:02 | 0 | |||
|
B6.129S7-In(11Trp53;11Wnt3)8Brd/Mmnc Resource Report Resource Website 1+ mentions |
RRID:MMRRC_000055-UNC | Mus musculus | Research areas: ; Mutation Type: inversion ; Collection: Mutagenesis for Dev. Defects/Baylor | prenatal lethality [MP:0011091]| increased tumor incidence [MP:0002020]| darkened coat color [MP:0005409] | 000055-UNC | inversion | Mutant Mouse Resource and Research Center (MMRRC) | MMRRC | PMID:10431243 | MMRRC_55-UNC, MMRRC_000055, MMRRC_55 | MMRRC | 2026-10-24 06:28:02 | 1 | ||||
|
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 | MMRRC | 2026-10-24 06:28:03 | 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 | MMRRC | 2026-10-24 06:28:03 | 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 | MMRRC | 2026-10-24 06:28:03 | 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 | MMRRC | 2026-10-24 06:28:03 | 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 | MMRRC | 2026-10-24 06:28:03 | 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 | MMRRC | 2026-10-24 06:28:03 | 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 | MMRRC | 2026-10-24 06:28:02 | 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 | MMRRC | 2026-10-24 06:28:03 | 0 |
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