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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Ercc2tm2(ERCC2)Jhjh/Ercc2tm2(ERCC2)Jhjh Resource Report The record is no longer available at this source. |
RRID:MGI:2386444 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | greasy coat, scaly skin, abnormal hair follicle morphology, alopecia, brittle hair, thick skin, postnatal growth retardation, acanthosis, hyperkeratosis, abnormal cell physiology, neoplasm, disproportionate dwarf, sparse hair, anemia, decreased bone mineral density, greasy coat, kyphosis, osteoporosis, abnormal epidermis stratum granulosum morphology, abnormal ovulation, osteoporosis, postnatal growth retardation, cachexia, anemia, abnormal circulating amino acid level, enlarged spleen, kyphosis, premature death, white spotting, cachexia, abnormal sebaceous gland morphology, hyperkeratosis, premature aging, decreased hemoglobin content, decreased hematocrit, decreased erythrocyte cell number, enlarged sebaceous gland, reduced female fertility, reduced female fertility, abnormal coat/ hair morphology, brittle hair, acanthosis, tremors, cachexia, abnormal skeleton morphology, premature death, abnormal fat cell morphology, enlarged hair follicles, increased incidence of induced tumors | Ercc2 | tm2(ERCC2)Jhjh | 2386444 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9651581 PMID:16904611 PMID:17020410 PMID:11950998 |
2024-01-30 12:21:07 | 0 | ||
|
Alox15tm1Fun/Alox15tm1Fun Resource Report The record is no longer available at this source. |
RRID:MGI:2429456 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | reproductive system phenotype, endocrine/exocrine gland phenotype, abnormal immune system physiology, hematopoietic system phenotype | Alox15 | tm1Fun | 2429456 | involves: 129/Sv * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:8798642 | 2024-01-30 12:21:06 | 0 | ||
|
Adrb1tm1Bkk/Adrb1tm1Bkk; Adrb3tm1Lowl/Adrb3tm1Lowl; Adrb2tm1Bkk/Adrb2tm1Bkk Resource Report The record is no longer available at this source. |
RRID:MGI:2388265 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | increased brown fat cell size, increased interscapular fat pad weight, impaired adaptive thermogenesis, abnormal brown adipose tissue morphology, endocrine/exocrine gland phenotype, increased total body fat amount, increased body weight, increased circulating leptin level, obese, decreased oxygen consumption | Adrb2, Adrb3, Adrb1 | tm1Lowl, tm1Bkk | 2388265 | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2 * FVB/N | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12161655 | 2024-01-30 12:21:50 | 0 | ||
|
Aifm1Hq Resource Report The record is no longer available at this source. |
RRID:MGI:2387326 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | abnormal eye electrophysiology, increased superoxide dismutase level, abnormal myocardial fiber physiology, decreased susceptibility to neuronal excitotoxicity, altered response to myocardial infarction, oxidative stress, cardiac hypertrophy, decreased cardiac muscle contractility, thin retinal outer plexiform layer, retinal degeneration, oxidative stress, small cerebellum, abnormal respiratory electron transport chain, amacrine cell degeneration, abnormal cardiovascular system morphology, decreased birth weight, ataxia, alopecia, retinal ganglion cell degeneration, dilated heart left ventricle, increased cellular sensitivity to hydrogen peroxide, abnormal cerebellar cortex morphology, decreased body size, increased cardiomyocyte apoptosis, abnormal cerebellar granule layer morphology, decreased body weight, Purkinje cell degeneration, impaired coordination, abnormal cell cycle, thin retinal inner plexiform layer, abnormal cerebellar granule cell morphology, increased catalase activity, premature death, tremors, sparse hair, increased myocardial infarction size, increased catalase activity, absent optic nerve, postnatal growth retardation, abnormal seizure response to pharmacological agent, abnormal cardiovascular system physiology, increased sensitivity to induced morbidity/mortality, ataxia, abnormal motor capabilities/coordination/movement, abnormal gait, abnormal cerebellar granule layer morphology, Purkinje cell degeneration | Aifm1 | Hq | 2387326 | B6CBACa A |
MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12353028 PMID:15703386 PMID:18791645 PMID:15933268 |
2024-01-30 12:21:06 | 0 | ||
|
Aifm1Hq/Aifm1Hq Resource Report The record is no longer available at this source. |
RRID:MGI:2387325 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | abnormal eye electrophysiology, retinal degeneration, abnormal cerebellar granule cell morphology, increased catalase activity, abnormal cell cycle, retinal ganglion cell degeneration, amacrine cell degeneration, abnormal cerebellar granule layer morphology, Purkinje cell degeneration, increased cellular sensitivity to hydrogen peroxide, small cerebellum, abnormal cerebellar cortex morphology, oxidative stress, thin retinal inner plexiform layer, Purkinje cell degeneration, abnormal seizure response to pharmacological agent, alopecia, ataxia, decreased birth weight, increased catalase activity, absent optic nerve, abnormal cerebellar granule layer morphology, abnormal gait, abnormal motor capabilities/coordination/movement, ataxia, tremors, sparse hair, decreased susceptibility to neuronal excitotoxicity, oxidative stress, increased sensitivity to induced morbidity/mortality, abnormal cardiovascular system morphology, abnormal respiratory electron transport chain, decreased body size, decreased body weight, impaired coordination, increased superoxide dismutase level, premature death, abnormal myocardial fiber physiology, cardiac hypertrophy, dilated heart left ventricle, abnormal cardiovascular system physiology, altered response to myocardial infarction, increased myocardial infarction size, increased cardiomyocyte apoptosis, decreased cardiac muscle contractility, thin retinal outer plexiform layer | Aifm1 | Hq | 2387325 | B6CBACa A |
MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12353028 PMID:15703386 PMID:18791645 PMID:15933268 |
2024-01-30 12:21:35 | 0 | ||
|
Adipoqtm1Tka/Adipoq+ Resource Report The record is no longer available at this source. |
RRID:MGI:2387163 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | insulin resistance, impaired glucose tolerance | Adipoq | tm1Tka | 2387163 | involves: 129S4/SvJae * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12032136 | 2024-01-30 12:21:06 | 0 | ||
|
Tbcepmn/Tbcepmn Resource Report The record is no longer available at this source. |
RRID:MGI:2429569 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | motor neuron degeneration, abnormal facial nerve morphology, premature death, paralysis, abnormal phrenic nerve morphology, premature death, respiratory failure, progressive muscle weakness, axon degeneration, muscular atrophy, respiratory failure | Tbce | pmn | 2429569 | NMRI/Pan | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:1641039 PMID:2022963 |
2024-01-30 12:21:06 | 0 | ||
|
C3tm1Crr/C3tm1Crr Resource Report The record is no longer available at this source. |
RRID:MGI:2429606 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | increased circulating alanine transaminase level, decreased circulating alanine transaminase level, focal hepatic necrosis, increased circulating bilirubin level, decreased susceptibility to injury, immune system phenotype, decreased liver regeneration, decreased circulating interleukin-6 level, decreased osteoclast cell number, abnormal liver physiology, abnormal induced morbidity/mortality, abnormal enzyme/coenzyme level, abnormal spleen germinal center morphology, decreased spleen germinal center number, decreased circulating interleukin-6 level, hepatic steatosis, decreased spleen germinal center size, decreased circulating tumor necrosis factor level, decreased mast cell number, abnormal peripheral nervous system regeneration, increased susceptibility to bacterial infection induced morbidity/mortality, abnormal humoral immune response, abnormal mast cell physiology, abnormal cell-mediated immunity, liver inflammation, increased susceptibility to bacterial infection, decreased vascular permeability, abnormal intestine morphology, decreased neutrophil cell number, increased susceptibility to bacterial infection, abnormal tumor necrosis factor level, decreased hepatocyte proliferation, abnormal liver morphology, abnormal immune system morphology, abnormal immune system physiology, increased sensitivity to induced morbidity/mortality | C3 | tm1Crr | 2429606 | involves: 129S4/SvJae * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9367154 PMID:10811844 PMID:10066708 PMID:19620784 PMID:20709903 PMID:16936276 PMID:8524789 PMID:23733878 PMID:8752901 |
2024-01-30 12:21:06 | 0 | ||
|
Pax6tm1Pgr/Pax6tm1Pgr Resource Report The record is no longer available at this source. |
RRID:MGI:2386628 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal neuron physiology, abnormal spinal cord interneuron morphology, abnormal CNS synaptic transmission | Pax6 | tm1Pgr | 2386628 | involves: 129S1/Sv * 129X1/SvJ | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:16525473 | 2024-01-30 12:21:07 | 0 | ||
|
Atp7aMo-12H/Atp7a+ Resource Report The record is no longer available at this source. |
RRID:MGI:2387678 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | abnormal limb bone morphology, impaired balance, curly vibrissae, variegated coat color, impaired coordination | Atp7a | Mo-12H | 2387678 | involves: 101/H * C3H/HeH | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | 2024-01-30 12:21:06 | 0 | |||
|
Atp7aMo-12H Resource Report The record is no longer available at this source. |
RRID:MGI:2387677 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | preweaning lethality, complete penetrance | Atp7a | Mo-12H | 2387677 | involves: 101/H * C3H/HeH | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | 2024-01-30 12:21:06 | 0 | |||
|
Uncv/Uncv Resource Report The record is no longer available at this source. |
RRID:MGI:2387312 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | slow postnatal weight gain, enlarged sebaceous gland, decreased litter size, azoospermia, hairless | Uncv | Uncv | 2387312 | involves: BALB/c | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10425919 | 2024-01-30 12:21:50 | 0 | ||
|
Atp7aMo-11H/Atp7a+ Resource Report The record is no longer available at this source. |
RRID:MGI:2387673 | Mus musculus | Allele Detail: Chemically and radiation induced This is a legacy resource. | perinatal lethality, incomplete penetrance, variegated coat color | Atp7a | Mo-11H | 2387673 | involves: 101/H * C3H/HeH | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | 2024-01-30 12:21:35 | 0 | |||
|
KitW/KitW-v Resource Report The record is no longer available at this source. |
RRID:MGI:2387552 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | increased papilloma incidence, abnormal response to transplant, peptic ulcer, increased esophageal papilloma incidence | Kit | W, W-v | 2387552 | involves: C57BL/6 * WB | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:7000343 PMID:367470 |
2024-01-30 12:21:06 | 0 | ||
|
KitW-v/Kit+ Resource Report The record is no longer available at this source. |
RRID:MGI:2387551 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | macrocytic anemia | Kit | W-v | 2387551 | involves: C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:15393917 | 2024-01-30 12:21:06 | 0 | ||
|
Atp7aMo-10H Resource Report The record is no longer available at this source. |
RRID:MGI:2387670 | Mus musculus | Allele Detail: Chemically and radiation induced This is a legacy resource. | postnatal lethality, complete penetrance, curly vibrissae, absent coat pigmentation, impaired coordination | Atp7a | Mo-10H | 2387670 | involves: 101/H * C3H/HeH | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | 2024-01-30 12:21:06 | 0 | |||
|
Cln8mnd/Cln8mnd Resource Report The record is no longer available at this source. |
RRID:MGI:2388401 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | premature death, abnormal motor neuron morphology, abnormal nervous system morphology, premature death, retinal degeneration, abnormal retinal photoreceptor layer morphology, short photoreceptor inner segment, thin retinal outer nuclear layer, abnormal retinal pigment epithelium morphology, abnormal retinal rod cell inner segment morphology, abnormal retinal rod cell outer segment morphology, short photoreceptor outer segment | Cln8 | mnd | 2388401 | involves: AKR/J * B6.KB2 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10191135 PMID:1639406 PMID:8282051 |
2024-01-30 12:21:35 | 0 | ||
|
Tg(Ren2-TAg)4Kwg Resource Report The record is no longer available at this source. |
RRID:MGI:2389579 | Mus musculus | Allele Detail: Transgenic This is a legacy resource. | abnormal kidney blood vessel morphology, preneoplasia, increased sarcoma incidence, increased tumor incidence | Tg(Ren2-TAg)4Kwg | Tg(Ren2-TAg)4Kwg | 2389579 | involves: C3H/HeRos * C57BL/10Ros | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:1996675 PMID:2172970 |
2024-01-30 12:21:06 | 0 | ||
|
Rab3aEbd/Rab3aEbd Resource Report The record is no longer available at this source. |
RRID:MGI:2388807 | Mus musculus | Allele Detail: Chemically induced (ENU) This is a legacy resource. | shortened circadian behavior period | Rab3a | Ebd | 2388807 | C57BL/6J-Rab3a |
MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12244319 | 2024-01-30 12:21:06 | 0 | ||
|
Rab3aEbd/Rab3a+ Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2388809 | Mus musculus | Allele Detail: Chemically induced (ENU) This is a legacy resource. | shortened circadian behavior period | Rab3a | Ebd | 2388809 | involves: C3H/HeJ * C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12244319 | 2024-01-30 12:21:06 | 1 |
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