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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Pthlhtm1Hmk/Pthlhtm1Hmk; Pthtm1Dgo/Pthtm1Dgo Resource Report The record is no longer available at this source. |
RRID:MGI:2665233 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | increased chondrocyte apoptosis, abnormal angiogenesis, short limbs, abnormal bone mineralization, abnormal trabecular bone morphology, decreased osteoblast cell number, abnormal osteoclast morphology, abnormal skeleton morphology, decreased length of long bones, enlarged parathyroid gland, increased osteocyte apoptosis, abnormal axial skeleton morphology, abnormal bone structure, increased compact bone thickness, abnormal long bone hypertrophic chondrocyte zone, perinatal lethality, complete penetrance, disproportionate dwarf, decreased osteoclast cell number, abnormal appendicular skeleton morphology, increased width of hypertrophic chondrocyte zone, increased osteoblast apoptosis, abnormal long bone epiphyseal plate proliferative zone, abnormal cartilage development | Pthlh, Pth | tm1Dgo, tm1Hmk | 2665233 | involves: 129S2/SvPas * C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11994406 | 2024-01-30 12:20:58 | 0 | ||
|
Tg(Tcra/Tcrb)3Ayr Resource Report The record is no longer available at this source. |
RRID:MGI:2665511 | Mus musculus | Allele Detail: Transgenic This is a legacy resource. | abnormal lymphocyte anergy, decreased T cell proliferation, abnormal positive T cell selection | Tg(Tcra, Tcrb)3Ayr | 2665511 | involves: C57BL/6 * DBA/2 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10843678 PMID:12460193 |
2024-01-30 12:20:58 | 0 | |||
|
Mgat2tm1.1Jxm/Mgat2tm1.1Jxm Resource Report The record is no longer available at this source. |
RRID:MGI:2667777 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal muscle development, anemia, decreased circulating total protein level, nervous system phenotype, abnormal blood coagulation, increased mean corpuscular volume, hypoglycemia, reticulocytosis, decreased circulating calcium level, abnormal digestion, gastrointestinal hemorrhage, abnormal facial morphology, delayed bone ossification, abnormal locomotor behavior, postnatal lethality, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance, rectal prolapse, kyphoscoliosis, paralysis, decreased body size, decreased bone mineral density, decreased fetal size, tremors, abnormal PNS synaptic transmission | Mgat2 | tm1.1Jxm | 2667777 | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11805078 | 2024-01-30 12:21:29 | 0 | ||
|
Rag2tm1Fwa/Rag2tm1Fwa; Trp53tm1Tyj/Trp53tm1Tyj Resource Report The record is no longer available at this source. |
RRID:MGI:2665118 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | premature death, increased T cell derived lymphoma incidence | Rag2, Trp53 | tm1Fwa, tm1Tyj | 2665118 | involves: 129S/SvEv * 129S2/SvPas * C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9584189 | 2024-01-30 12:20:58 | 0 | ||
|
Pcsk4tm1Mbi/Pcsk4tm1Mbi Resource Report The record is no longer available at this source. |
RRID:MGI:2665513 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | reduced female fertility, decreased litter size, transmission ratio distortion, reduced male fertility, reduced hyperactivated sperm motility, impaired fertilization | Pcsk4 | tm1Mbi | 2665513 | involves: 129P2/OlaHsd * C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9192653 | 2024-01-30 12:20:58 | 0 | ||
|
Acvr2atm1Zuk/Acvr2atm1Zuk Resource Report The record is no longer available at this source. |
RRID:MGI:2665042 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal spermatid morphology, abnormal Sertoli cell morphology, decreased male germ cell number, decreased testis weight, abnormal spermatogonia morphology | Acvr2a | tm1Zuk | 2665042 | involves: 129S7/SvEvBrd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11416011 | 2024-01-30 12:20:58 | 0 | ||
|
Adam3tm1Ihgg/Adam3tm1Ihgg Resource Report The record is no longer available at this source. |
RRID:MGI:2665287 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | male infertility, reproductive system phenotype, impaired acrosome reaction | Adam3 | tm1Ihgg | 2665287 | involves: 129S1/Sv * 129X1/SvJ * CD-1 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10569988 | 2024-01-30 12:20:58 | 0 | ||
|
Pou3f1tm1Rsd/Pou3f1tm1Rsd Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2665327 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | postnatal lethality, complete penetrance | Pou3f1 | tm1Rsd | 2665327 | involves: 129/Sv * 129S4/SvJae * C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:8698235 | 2024-01-30 12:20:58 | 1 | ||
|
Coq7tm1Hek/Coq7tm1Hek Resource Report The record is no longer available at this source. |
RRID:MGI:2665329 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased embryo size, embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance | Coq7 | tm1Hek | 2665329 | involves: 129S1/Sv * 129X1/SvJ | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11585841 | 2024-01-30 12:20:58 | 0 | ||
|
Il10tm1Cgn/Il10tm1Cgn Resource Report The record is no longer available at this source. |
RRID:MGI:2665845 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal leukocyte morphology, intestinal inflammation, decreased physiological sensitivity to xenobiotic, abnormal type IV hypersensitivity reaction, decreased tumor incidence, decreased incidence of tumors by UV induction, decreased T cell proliferation, abnormal intestinal epithelium morphology, thymus hyperplasia, intestinal inflammation, increased thymus weight, immune system phenotype, abnormal tumor necrosis factor level, abnormal interleukin level, abnormal interferon level, abnormal colon morphology, increased large intestine adenocarcinoma incidence, large intestinal inflammation, abnormal cytokine level, increased CD4-positive, alpha beta T cell number, abnormal immune system physiology, colitis, increased intestinal adenocarcinoma incidence, abnormal intestinal mucosa morphology, abnormal interleukin level, small intestinal inflammation, cecum inflammation, abnormal tumor necrosis factor level, abnormal large intestine morphology, abnormal interferon level, alveolar process atrophy, abnormal nitric oxide homeostasis, decreased airway responsiveness, abnormal lymphocyte cell number, enhanced wound healing, increased susceptibility to parasitic infection, increased granulocyte number, abnormal interferon level, abnormal protein level, decreased circulating insulin level, increased circulating cholesterol level, increased fatty acid level, increased insulin sensitivity, decreased length of allograft survival, abnormal tumor necrosis factor level, abnormal Langerhans cell physiology, increased susceptibility to type IV hypersensitivity reaction, abnormal interleukin level, increased hepatocyte apoptosis, abnormal circulating enzyme level, abnormal circulating protein level, abnormal placental labyrinth vasculature morphology, decreased circulating creatinine level, short femur, decreased trabecular bone thickness, increased placental labyrinth size, decreased trabecular bone mass, increased liver triglyceride level, decreased circulating cholesterol level, abnormal homeostasis, abnormal bone mineralization, decreased bone trabecula number, increased myocardial infarction size, intestinal inflammation, abnormal glucose homeostasis, increased IgE level, decreased airway responsiveness, increased leukotriene level, increased IgG1 level, increased IgG2a level, decreased compact bone mass, abnormal osteoblast differentiation, abnormal skeleton morphology, abnormal skeleton physiology, decreased bone mineral content, decreased bone strength, abnormal bone structure, abnormal trabecular bone morphology, abnormal circulating serum albumin level, abnormal liver physiology, abnormal lipid level, increased thermal nociceptive threshold, immune system phenotype, increased interferon-gamma secretion, postnatal growth retardation, decreased spleen iron level, cachexia, premature death, microcytic anemia, increased granulocyte number, chronic inflammation, anemia, decreased erythrocyte cell number, abnormal myelopoiesis, absent erythroid progenitor cell, abnormal level of surface class II molecules, abnormal response to infection, abnormal crypts of Lieberkuhn morphology, decreased spleen red pulp amount, abnormal iron level, decreased circulating iron level, hypochromic anemia, decreased hemoglobin content, abnormal intestinal mucosa morphology, abnormal enterocyte morphology | Il10 | tm1Cgn | 2665845 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:16476050 PMID:15618456 PMID:16709607 PMID:12842419 PMID:11406467 PMID:9886396 PMID:12799032 PMID:8402911 PMID:16497487 PMID:17200193 PMID:9366559 PMID:8770874 PMID:17305866 PMID:8823360 PMID:10811896 PMID:15362035 PMID:17579057 PMID:11285204 PMID:17600128 |
2024-01-30 12:20:58 | 0 | ||
|
Twist1tm1Bhr/Twist1+ Resource Report The record is no longer available at this source. |
RRID:MGI:2667352 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | temporal bone hypoplasia, abnormal limb morphology, craniofacial phenotype, premature cranial suture closure, premature coronal suture closure | Twist1 | tm1Bhr | 2667352 | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12221714 | 2024-01-30 12:21:29 | 0 | ||
|
Fgf18tm1Sjt/Fgf18tm1Sjt Resource Report The record is no longer available at this source. |
RRID:MGI:2667630 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | perinatal lethality, complete penetrance, abnormal rib morphology, delayed bone ossification, abnormal lung saccule morphology, small thoracic cavity, short tibia, short ulna, abnormal fibula morphology, abnormal lung development, kyphosis, delayed cranial suture closure, small lung lobe, short radius, thick lung-associated mesenchyme, abnormal lung vasculature morphology, small lung | Fgf18 | tm1Sjt | 2667630 | involves: 129S1/Sv * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11937494 PMID:15336546 |
2024-01-30 12:20:58 | 0 | ||
|
En1tm1Alj/En1tm1Alj Resource Report The record is no longer available at this source. |
RRID:MGI:2667359 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | En1 | tm1Alj | 2667359 | either: (involves: 129) or (involves: 129 * C57BL/6J) | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | 2024-01-30 12:20:58 | 0 | ||||
|
Fras1tm1Chpk/Fras1tm1Chpk Resource Report The record is no longer available at this source. |
RRID:MGI:2667203 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | lethality throughout fetal growth and development, complete penetrance, absent kidney, blistering, syndactyly, cryptophthalmos, lethality throughout fetal growth and development, incomplete penetrance | Fras1 | tm1Chpk | 2667203 | involves: 129S1/Sv * 129X1/SvJ * C57BL/10 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12766770 | 2024-01-30 12:20:58 | 0 | ||
|
Cited2tm1Ycy/Cited2+ Resource Report The record is no longer available at this source. |
RRID:MGI:2667201 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased embryo size, prenatal lethality, incomplete penetrance, exencephaly | Cited2 | tm1Ycy | 2667201 | involves: C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12149478 | 2024-01-30 12:20:58 | 0 | ||
|
Tg(RBP3-TAg)#Ove Resource Report The record is no longer available at this source. |
RRID:MGI:2665147 | Mus musculus | Allele Detail: Transgenic This is a legacy resource. | increased tumor incidence, increased retina tumor incidence, increased brain tumor incidence, retinal detachment | Tg(RBP3-TAg)#Ove | 2665147 | involves: C57BL/6 * FVB/N | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:1334963 | 2024-01-30 12:20:58 | 0 | |||
|
Tll1tm1Dgr/Tll1tm1Dgr; Bmp1tm1Blh/Bmp1tm1Blh Resource Report The record is no longer available at this source. |
RRID:MGI:2667447 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | prenatal lethality, complete penetrance, congestive heart failure, abnormal heart position or orientation, muscular ventricular septal defect, abnormal aorta morphology | Tll1, Bmp1 | tm1Dgr, tm1Blh | 2667447 | involves: 129 * Black Swiss | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12808086 | 2024-01-30 12:20:58 | 0 | ||
|
Tg(Fabp2-Arg1)1Wla/Tg(Fabp2-Arg1)1Wla Resource Report The record is no longer available at this source. |
RRID:MGI:2665306 | Mus musculus | Allele Detail: Transgenic This is a legacy resource. | decreased B cell number, delayed hair appearance, abnormal Peyer's patch morphology, sparse hair, abnormal enterocyte physiology, decreased arginine level, increased circulating glycine level, increased ornithine level, abnormal amino acid level, hyperkeratosis, distorted hair follicle pattern, decreased circulating arginine level, decreased transitional stage B cell number, abnormal B cell differentiation, abnormal Peyer's patch morphology, decreased IgM level, abnormal epidermal layer morphology, abnormal enzyme/coenzyme activity, abnormal spleen B cell follicle morphology, decreased Peyer's patch number, decreased skeletal muscle fiber diameter, postnatal growth retardation, hyperactivity, decreased spleen weight, abnormal hair follicle morphology, small Peyer's patches, decreased body weight, decreased pre-B cell number, small spleen | Tg(Fabp2-Arg1)1Wla | 2665306 | involves: FVB | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12438451 PMID:12081826 |
2024-01-30 12:20:58 | 0 | |||
|
Rargtm1Ipc/Rargtm1Ipc Resource Report The record is no longer available at this source. |
RRID:MGI:2665708 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal keratinocyte morphology, abnormal prostate gland morphology, squamous metaplasia of prostate gland, premature death, squamous metaplasia of seminal vesicles, decreased survivor rate, abnormal skeleton development, abnormal cervical vertebrae morphology, male infertility, abnormal eyelid morphology, fusion of atlas and occipital bones, seminal vesicle atrophy, abnormal Harderian gland morphology, vertebral transformation, thoracic vertebral transformation, rib fusion, fusion of vertebral arches, fused tracheal cartilage rings, cervical vertebral transformation, decreased body weight, postnatal growth retardation, abnormal axial skeleton morphology, abnormal epidermis stratum corneum morphology, shiny skin, impaired skin barrier function, abnormal response to vitamins, abnormal epidermal lamellar body morphology, fused tracheal cartilage rings, abnormal cricoid cartilage morphology | Rarg | tm1Ipc | 2665708 | involves: 129S2/SvPas | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:16751185 PMID:8388780 PMID:9376317 |
2024-01-30 12:20:58 | 0 | ||
|
Ikzf1tm1Kast/Ikzf1tm1Kast Resource Report The record is no longer available at this source. |
RRID:MGI:2667178 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased spleen germinal center number, decreased B-1b cell number, decreased IgG3 level, decreased B-1a cell number, abnormal B cell activation, abnormal B cell differentiation, decreased B cell number, decreased B cell proliferation | Ikzf1 | tm1Kast | 2667178 | involves: 129S2/SvPas | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11870616 | 2024-01-30 12:20:58 | 0 |
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