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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 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Slc6a3tm1Mca/Slc6a3tm1Mca Resource Report The record is no longer available at this source. |
RRID:MGI:2654500 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | postnatal growth retardation, decreased length of long bones, decreased dopamine level, hypopituitarism, decreased vertical activity, premature death, decreased dopamine level, hyperactivity, hyperactivity, abnormal maternal nurturing, impaired coordination, decreased dopaminergic neuron number, abnormal pituitary gland physiology, short stride length, lactation failure, pituitary intermediate lobe hypoplasia, abnormal pituitary secretion, decreased body weight, postnatal growth retardation, adenohypophysis hypoplasia, disproportionate dwarf, decreased somatotroph cell number, decreased lactotroph cell number, abnormal adenohypophysis morphology, abnormal spatial learning, hyperactivity, decreased dopamine level, decreased dopaminergic neuron number, decreased dopamine level, decreased body size, increased thigmotaxis | Slc6a3 | tm1Mca | 2654500 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12617953 PMID:8628395 PMID:9888856 PMID:9520487 PMID:9247269 PMID:10564358 |
MGI | 2024-01-30 12:21:03 | 0 | ||
|
Ror2tm1Gdy/Ror2tm1Gdy Resource Report The record is no longer available at this source. |
RRID:MGI:2654730 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal vertebrae morphology, short nasal bone, abnormal hindlimb stylopod morphology, delayed endochondral bone ossification, rib fusion, abnormal digit development, abnormal radius morphology, short lumbar vertebrae, abnormal phalanx morphology, delayed endochondral bone ossification, abnormal tail morphology, brachydactyly, abnormal long bone epiphyseal plate proliferative zone, abnormal caudal vertebrae morphology, abnormal limb development, abnormal vertebral column morphology, abnormal endochondral bone ossification, abnormal femur morphology, abnormal limb development, abnormal skeleton development, abnormal humerus morphology, cleft palate, perinatal lethality, complete penetrance, short femur, short humerus, short limbs, short snout, short tail, abnormal long bone morphology, abnormal fibula morphology, abnormal tibia morphology, abnormal ulna morphology, abnormal long bone epiphyseal plate morphology, increased width of hypertrophic chondrocyte zone, small caudal vertebrae, short fibula, short radius, short tibia, short ulna | Ror2 | tm1Gdy | 2654730 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:18353862 PMID:10700181 |
MGI | 2024-01-30 12:21:02 | 0 | ||
|
Ror2tm1Gdy/Ror2+ Resource Report The record is no longer available at this source. |
RRID:MGI:2654731 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | Ror2 | tm1Gdy | 2654731 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | MGI | 2024-01-30 12:21:02 | 0 | ||||
|
Mertktm1Grl/Mertktm1Grl Resource Report The record is no longer available at this source. |
RRID:MGI:2654780 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased Sertoli cell phagocytosis, enlarged spleen, cardiovascular system phenotype, vagina atresia, blindness, abnormal photoreceptor outer segment morphology, retinal photoreceptor degeneration, abnormal retinal pigment epithelium morphology, disorganized photoreceptor outer segment | Mertk | tm1Grl | 2654780 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:19729839 PMID:16901715 PMID:18159085 PMID:10227296 PMID:18393392 |
MGI | 2024-01-30 12:21:02 | 0 | ||
|
Hprttm1(ACTB-Epor)Unc Resource Report The record is no longer available at this source. |
RRID:MGI:2653304 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal definitive hematopoiesis, hematopoietic system phenotype | Hprt | tm1(ACTB-Epor)Unc | 2653304 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:8790342 | MGI | 2024-01-30 12:21:03 | 0 | ||
|
H2-DMatm1Lkrl/H2-DMatm1Lkrl Resource Report The record is no longer available at this source. |
RRID:MGI:2652161 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal professional antigen presenting cell physiology, abnormal positive T cell selection, decreased CD4-positive, alpha beta T cell number, abnormal antigen presentation, abnormal CD4-positive, alpha-beta T cell physiology | H2-DMa | tm1Lkrl | 2652161 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:8638109 | MGI | 2024-01-30 12:21:04 | 0 | ||
|
Srftm2Nor/Srftm2Nor Resource Report The record is no longer available at this source. |
RRID:MGI:2449176 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | no abnormal phenotype detected | Srf | tm2Nor | 2449176 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11857797 | MGI | 2024-01-30 12:21:06 | 0 | ||
|
Ncam1tm1Cgn/Ncam1tm1Cgn Resource Report The record is no longer available at this source. |
RRID:MGI:2182567 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal spatial learning, decreased brain size, small olfactory bulb | Ncam1 | tm1Cgn | 2182567 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:8107803 | MGI | 2024-01-30 12:21:07 | 0 | ||
|
Nr5a1tm2Klp/Nr5a1tm2Klp Resource Report The record is no longer available at this source. |
RRID:MGI:2180103 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | no abnormal phenotype detected | Nr5a1 | tm2Klp | 2180103 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11124111 | MGI | 2024-01-30 12:21:08 | 0 | ||
|
Nr5a1tm2.1Klp/Nr5a1tm2.1Klp Resource Report The record is no longer available at this source. |
RRID:MGI:2180093 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | perinatal lethality, complete penetrance, agonadal, absent adrenal gland | Nr5a1 | tm2.1Klp | 2180093 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11124111 | MGI | 2024-01-30 12:21:08 | 0 | ||
|
Leprtm1.1Rck/Leprtm1.1Rck Resource Report The record is no longer available at this source. |
RRID:MGI:2176783 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | obese | Lepr | tm1.1Rck | 2176783 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11602618 | MGI | 2024-01-30 12:21:10 | 0 | ||
|
Tg(Msx2-cre)5Rem; Fgf4tm1.2Mrt/Fgf4tm1.3Mrt Resource Report The record is no longer available at this source. |
RRID:MGI:2176793 | Mus musculus | Allele Detail: Targeted, Transgenic This is a legacy resource. | no abnormal phenotype detected | Fgf4 | Tg(Msx2-cre)5Rem, tm1.2Mrt, tm1.3Mrt | 2176793 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10802662 | MGI | 2024-01-30 12:21:10 | 0 | ||
|
Tg(Msx2-cre)5Rem; Fgf8tm1.3Mrt/Fgf8tm1.4Mrt Resource Report The record is no longer available at this source. |
RRID:MGI:2176849 | Mus musculus | Allele Detail: Targeted, Transgenic This is a legacy resource. | abnormal hindlimb zeugopod morphology, abnormal forelimb stylopod morphology, abnormal forelimb zeugopod morphology, small limb buds, abnormal digit development, absent radius, abnormal hindlimb zeugopod morphology, abnormal hindlimb stylopod morphology, oligodactyly, abnormal limb development, abnormal hindlimb stylopod morphology, abnormal forelimb zeugopod morphology | Fgf8 | Tg(Msx2-cre)5Rem, tm1.4Mrt, tm1.3Mrt | 2176849 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:16308330 PMID:11101846 |
MGI | 2024-01-30 12:21:09 | 0 | ||
|
Fgf8tm1.2Mrt/Fgf8tm1.4Mrt Resource Report The record is no longer available at this source. |
RRID:MGI:2176824 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal mesoderm development, abnormal chorion morphology, abnormal amnion morphology, abnormal allantois morphology, absent primitive node, absent somites, absent heart, embryonic lethality during organogenesis, complete penetrance, abnormal primitive streak elongation, abnormal embryonic epiblast morphology, abnormal ectoderm development | Fgf8 | tm1.2Mrt, tm1.4Mrt | 2176824 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10421635 | MGI | 2024-01-30 12:21:10 | 0 | ||
|
Fgf8tm1.1Mrt/Fgf8tm1.2Mrt Resource Report The record is no longer available at this source. |
RRID:MGI:2176815 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal heart development, abnormal hypothalamus morphology, abnormal rostral-caudal axis patterning, absent cerebellum, prenatal lethality, incomplete penetrance, small embryonic telencephalon, abnormal pituitary gland morphology, abnormal craniofacial development, absent inferior colliculus, syndactyly, decreased embryo size, abnormal midbrain morphology | Fgf8 | tm1.2Mrt, tm1.1Mrt | 2176815 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9462741 PMID:21832120 |
MGI | 2024-01-30 12:21:10 | 0 | ||
|
Fgf8tm1.1Mrt/Fgf8tm1.1Mrt Resource Report The record is no longer available at this source. |
RRID:MGI:2176813 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | absent inferior colliculus, absent olfactory bulb, absent cerebellum, neonatal lethality, complete penetrance | Fgf8 | tm1.1Mrt | 2176813 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9462741 | MGI | 2024-01-30 12:21:10 | 0 | ||
|
Cd19tm1(cre)Cgn/Cd19tm1(cre)Cgn Resource Report The record is no longer available at this source. |
RRID:MGI:2175750 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal B cell physiology, absent spleen germinal center, abnormal immunoglobulin level, decreased IgM level, decreased B-1 B cell number, absent spleen germinal center, decreased IgG1 level, decreased IgE level, abnormal B cell differentiation, decreased B-1 B cell number | Cd19 | tm1(cre)Cgn | 2175750 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:7543183 PMID:12563260 |
MGI | 2024-01-30 12:21:11 | 0 | ||
|
Psen1tm1Bdes/Psen1tm1Bdes Resource Report The record is no longer available at this source. |
RRID:MGI:2174990 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal sagittal suture morphology, intracerebral hemorrhage, abnormal body wall morphology, abnormal neurocranium morphology, decreased Cajal-Retzius cell number, omphalocele, abnormal meninges morphology, fetal growth retardation, lethality throughout fetal growth and development, complete penetrance, abnormal cerebral cortex morphology, abnormal brain vasculature morphology, abnormal cortical marginal zone morphology, short tail, abnormal neuronal migration | Psen1 | tm1Bdes | 2174990 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10421573 PMID:9450754 |
MGI | 2024-01-30 12:21:13 | 0 | ||
|
Tcf7tm2Cle/Tcf7tm2Cle Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2174760 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased double-positive T cell number, decreased single-positive T cell number, thymus hypoplasia | Tcf7 | tm2Cle | 2174760 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:7870176 | MGI | 2024-01-30 12:21:14 | 1 | ||
|
Nrg1tm2Cbm/Nrg1tm2Cbm Resource Report The record is no longer available at this source. |
RRID:MGI:2173313 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal sympathetic ganglion morphology, decreased Schwann cell number, abnormal neural crest cell migration | Nrg1 | tm2Cbm | 2173313 | involves: 129P2/OlaHsd | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9637684 PMID:9342050 |
MGI | 2024-01-30 12:21:14 | 0 |
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