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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Foxn1nu/Foxn1nu Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2662818 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | abnormal coat/ hair morphology, abnormal embryonic tissue morphology, abnormal hair shaft morphology, abnormal corneocyte morphology, abnormal hair follicle inner root sheath morphology, abnormal hair cuticle, abnormal hair follicle morphology, abnormal epidermis stratum granulosum morphology, abnormal epidermal layer morphology, short nails, abnormal nail matrix morphology, deformed nails, abnormal nail plate morphology, nail dystrophy, abnormal nail morphology, endocrine/exocrine gland phenotype, abnormal thymus development, abnormal cutaneous collagen fibril morphology, abnormal hair cortex morphology, abnormal epidermis stratum basale morphology, abnormal epidermis stratum corneum morphology, reduced hair shaft melanin granule number, abnormal hair cortex keratinization | Foxn1 | nu | 2662818 | involves: NMRI | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:15610506 PMID:7405870 PMID:2288204 |
MGI | 2024-01-30 12:20:59 | 1 | ||
|
Msh4tm1Wed/Msh4tm1Wed; Msh5tm1Rak/Msh5tm1Rak Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2663948 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | female infertility, male infertility, abnormal male meiosis | Msh4, Msh5 | tm1Rak, tm1Wed | 2663948 | involves: 129/Sv * C57BL/6 * SJL | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10809667 | MGI | 2024-01-30 12:20:59 | 1 | ||
|
Cnr2tm1Zim/Cnr2tm1Zim Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2663848 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal macrophage physiology, immune system phenotype | Cnr2 | tm1Zim | 2663848 | involves: 129 * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10822068 | MGI | 2024-01-30 12:20:59 | 2 | ||
|
Chrnb2tm1Mdb/Chrnb2tm1Mdb Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2663180 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | no abnormal phenotype detected | Chrnb2 | tm1Mdb | 2663180 | involves: 129S7/SvEvBrd * C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10531434 | MGI | 2024-01-30 12:20:59 | 1 | ||
|
Rac1tm1.1Djk/Rac1tm1.1Djk Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2663672 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | embryonic lethality between somite formation and embryo turning, complete penetrance | Rac1 | tm1.1Djk | 2663672 | involves: 129S4/SvJae * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12759446 | MGI | 2024-01-30 12:21:29 | 1 | ||
|
Bak1tm1Thsn/Bak1tm1Thsn Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2656013 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | no abnormal phenotype detected | Bak1 | tm1Thsn | 2656013 | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11163212 | MGI | 2024-01-30 12:21:01 | 1 | ||
|
Bmp2tm1Brd/Bmp2tm1Brd Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2658703 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | open neural tube, abnormal chorion morphology, incomplete embryo turning, decreased embryo size, delayed allantois development, delayed heart development, abnormal heart development, abnormal heart position or orientation, abnormal proamniotic cavity morphology, embryonic lethality, complete penetrance | Bmp2 | tm1Brd | 2658703 | involves: 129S7/SvEvBrd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:8898212 | MGI | 2024-01-30 12:21:01 | 1 | ||
|
Il4ratm1Fbb/Il4ratm1Fbb Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2657175 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | altered susceptibility to infection | Il4ra | tm1Fbb | 2657175 | involves: BALB/c | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10358179 | MGI | 2024-01-30 12:21:01 | 1 | ||
|
Six1tm1Mair/Six1tm1Mair Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2655196 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal intercostal muscle morphology, abnormal muscle fiber morphology, rib fusion, abnormal genioglossus muscle morphology, abnormal sternum ossification, abnormal hypaxial muscle morphology, abnormal rib morphology, abnormal sternocostal joint morphology, decreased skeletal muscle mass, decreased tongue size, perinatal lethality, complete penetrance, rib bifurcation, abnormal myogenesis, muscle hypoplasia, thin diaphragm muscle, abnormal xiphoid process morphology | Six1 | tm1Mair | 2655196 | either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12668636 | MGI | 2024-01-30 12:21:02 | 1 | ||
|
Tg(Thy1-SNCA*A30P)18Pjk/Tg(Thy1-SNCA*A30P)18Pjk Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2652214 | Mus musculus | Allele Detail: Transgenic This is a legacy resource. | hindlimb paralysis, gliosis, hunched posture, abnormal tail movements, abnormal gait, abnormal locomotor behavior, progressive muscle weakness | Tg(Thy1-SNCA*A30P)18Pjk | 2652214 | involves: C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12438441 | MGI | 2024-01-30 12:21:04 | 3 | |||
|
Bsntm1Gund/Bsntm1Gund Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2652947 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal somatic nervous system physiology, clonic seizures, abnormal retinal rod cell morphology, absent active-zone-anchored inner hair cell synaptic ribbon, myoclonus, abnormal auditory brainstem response, abnormal synaptic transmission, decreased cochlear nerve compound action potential, abnormal cochlear inner hair cell physiology, impaired hearing, abnormal cochlear inner hair cell physiology, abnormal inner hair cell synaptic ribbon morphology, abnormal synaptic vesicle number, abnormal inner hair cell synaptic ribbon morphology, premature death, impaired righting response, decreased synaptic depression, convulsive seizures, ataxia, abnormal CNS synaptic transmission, abnormal brain wave pattern, increased susceptibility to pharmacologically induced seizures | Bsn | tm1Gund | 2652947 | Not Specified | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:21092861 PMID:15829963 PMID:12628169 PMID:22933801 |
MGI | 2024-01-30 12:21:04 | 1 | ||
|
C3ar1tm1Cge/C3ar1tm1Cge Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2449064 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased airway responsiveness, mortality/aging | C3ar1 | tm1Cge | 2449064 | involves: 129S4/SvJae * BALB/c | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10984054 | MGI | 2024-01-30 12:21:06 | 1 | ||
|
Hoxc9tm1Hsu/Hoxc9tm1Hsu Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2447619 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | postnatal growth retardation, abnormal thoracic vertebrae morphology, lumbar vertebral transformation, kyphosis, asymmetric sternocostal joints, increased rib number, abnormal sternum morphology, abnormal xiphoid process morphology | Hoxc9 | tm1Hsu | 2447619 | involves: 129S/SvEv * A/J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:7547473 | MGI | 2024-01-30 12:21:06 | 1 | ||
|
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 | MGI | 2024-01-30 12:21:06 | 1 | ||
|
Scnn1atm1.1Hum/Scnn1atm1.1Hum Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2386275 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | no abnormal phenotype detected | Scnn1a | tm1.1Hum | 2386275 | involves: 129 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11857811 | MGI | 2024-01-30 12:21:50 | 1 | ||
|
Smad3tm1Xfw/Smad3tm1Xfw Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2182651 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal sternum morphology, abnormal talus morphology, abnormal carpal bone morphology, kyphosis, abnormal cell proliferation, abnormal cytokine secretion, abnormal T cell proliferation, abnormal rib morphology, immune system phenotype, abnormal thoracic cage morphology, decreased body size, abnormal B cell proliferation | Smad3 | tm1Xfw | 2182651 | involves: 129/Sv * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10082515 | MGI | 2024-01-30 12:21:07 | 1 | ||
|
Tgfbr2tm1.1Hlm/Tgfbr2tm1.1Hlm Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2386217 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | preweaning lethality, complete penetrance | Tgfbr2 | tm1.1Hlm | 2386217 | involves: 129S6/SvEvTac * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11857781 | MGI | 2024-01-30 12:21:07 | 1 | ||
|
Snta1tm1Scf/Snta1tm1Scf Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2181419 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | muscle phenotype, abnormal astrocyte morphology, abnormal fluid regulation, decreased susceptibility to ischemic brain injury, abnormal nitric oxide homeostasis, abnormal neuromuscular synapse morphology | Snta1 | tm1Scf | 2181419 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12578959 PMID:10995443 |
MGI | 2024-01-30 12:21:36 | 1 | ||
|
Cacna1dtm1Jst/Cacna1dtm1Jst Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2181788 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | prolonged RR interval, deafness, decreased heart rate, heart block, prolonged PR interval, abnormal sinoatrial node conduction, deafness, increased heart rate, abnormal heart rate, prolonged PR interval, cochlear outer hair cell degeneration, cochlear inner hair cell degeneration, increased or absent threshold for auditory brainstem response, abnormal cochlear inner hair cell physiology, abnormal cochlear outer hair cell physiology, atrioventricular block, abnormal distortion product otoacoustic emission, increased or absent threshold for auditory brainstem response, abnormal sinus arrhythmia, mortality/aging, sinus bradycardia, increased heart rate variability, abnormal myocardial fiber physiology, abnormal sinoatrial node conduction, atrial fibrillation, atrioventricular block, abnormal action potential, cochlear ganglion degeneration, abnormal cochlear inner hair cell physiology, homeostasis/metabolism phenotype, sensorineural hearing loss, absent pinna reflex, cochlear outer hair cell degeneration, abnormal calcium ion homeostasis | Cacna1d | tm1Jst | 2181788 | involves: 129S7/SvEvBrd * C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:17074442 PMID:10929716 PMID:26831068 |
MGI | 2024-01-30 12:21:08 | 1 | ||
|
Klkl/Klkl Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2181617 | Mus musculus | Allele Detail: Transgenic This is a legacy resource. | hypoglycemia, abnormal bone structure, uterus atrophy, infertility, decreased subcutaneous adipose tissue amount, premature death, absent mature ovarian follicles, decreased somatotroph secretory granule number, abnormal adenohypophysis morphology, decreased insulin secretion, thin epidermis, premature aging, arteriosclerosis, postnatal growth retardation, decreased somatotroph cell size, thymus atrophy, kyphosis, abnormal gonadotroph morphology, calcified pulmonary alveolus, calcinosis, calcified muscle, osteoporosis, hypoactivity, abnormal blood circulation, decreased bone mineral density, decreased Purkinje cell number, decreased compact bone thickness, calcified skin, decreased osteoclast cell number, decreased hair follicle number, sparse hair, abnormal gametogenesis, abnormal seminiferous tubule morphology, external male genitalia atrophy, arrest of male meiosis, azoospermia, short stride length, Purkinje cell degeneration, vulva atrophy, increased circulating calcium level, ovary atrophy, abnormal bone ossification, emphysema, abnormal leukocyte cell number, abnormal circulating mineral level, abnormal skin condition, calcified artery, testicular atrophy | Kl | kl | 2181617 | either: C.Cg-Kl |
MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9363890 | MGI | 2024-01-30 12:21:08 | 1 |
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