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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Roratm1Mba/Roratm1Mba Resource Report The record is no longer available at this source. |
RRID:MGI:2174718 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | lethality at weaning, incomplete penetrance, small cerebellum, retarded hair growth, decreased grip strength, abnormal motor learning, limb grasping, absent duvet hair, ataxia, absent cerebellar granule cells, decreased Purkinje cell number, ectopic Purkinje cell, impaired coordination, abnormal cerebellar Purkinje cell layer, Purkinje cell degeneration, thin cerebellar granule layer, abnormal excitatory postsynaptic currents, sparse hair, abnormal Purkinje cell dendrite morphology | Rora | tm1Mba | 2174718 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9520475 | 2024-01-30 12:21:14 | 0 | ||
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Xrcc4tm1Fwa/Xrcc4tm1Fwa Resource Report The record is no longer available at this source. |
RRID:MGI:2174810 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | thymus hypoplasia, fetal growth retardation, abnormal cerebral cortex morphology, lethality throughout fetal growth and development, complete penetrance | Xrcc4 | tm1Fwa | 2174810 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9875844 | 2024-01-30 12:21:14 | 0 | ||
|
Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn Resource Report The record is no longer available at this source. |
RRID:MGI:2173367 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal salivary gland morphology, abnormal mammary placode morphology, submandibular gland hypoplasia, absent submandibular gland, abnormal rectum morphology, absent lungs, absent forelimb, absent hindlimb, absent rectum, abnormal perineum morphology, hypospadia, curly tail, cecal atresia, abnormal membranous labyrinth morphology, abnormal otic capsule morphology, abnormal semicircular canal morphology, small otic vesicle, absent eyelids, absent lungs, small scapula, premature squamoparietal suture closure, domed cranium, impaired branching involved in trachea morphogenesis, absent Rathke's pouch, abnormal Rathke's pouch apoptosis, absent adenohypophysis, absent hindlimb, translucent skin, small otic capsule, decreased skin pigmentation, abnormal pituitary gland development, abnormal lung development, caudal vertebral fusion, abnormal semicircular canal morphology, abnormal pelvic girdle bone morphology, abnormal stomach morphology, abnormal ilium morphology, abnormal epidermis stratum basale morphology, abnormal clavicle morphology, abnormal endolymphatic duct morphology, absent hypodermis muscle layer, inner ear cysts, abnormal ischium morphology, abnormal limb development, absent pubis, absent acromion, abnormal endolymphatic duct morphology, cleft palate, small stomach, thin dermal layer, thin epidermis, thin skin, abnormal Rathke's pouch development, arrest of tooth development, abnormal cecum development, absent forelimb, decreased body size, perinatal lethality, complete penetrance, curly tail, abnormal cochlea morphology, abnormal vestibulocochlear ganglion morphology, abnormal cochlear sensory epithelium morphology, abnormal epidermis stratum basale morphology, abnormal mammary gland bud morphology, absent mammary gland | Fgfr2 | tm1.1Dsn | 2173367 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10934262 PMID:14697353 PMID:11782400 PMID:10631169 PMID:16720875 PMID:15972105 PMID:15234214 |
2024-01-30 12:21:14 | 0 | ||
|
Foxc2tm1Miu/Foxc2tm1Miu Resource Report The record is no longer available at this source. |
RRID:MGI:2169410 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal supraoccipital bone morphology, absent cartilage, abnormal malleus morphology, abnormal vertebral arch morphology, abnormal aortic arch morphology, ventricular septal defect, abnormal middle ear ossicle morphology, abnormal pterygoid process morphology, abnormal fourth pharyngeal arch artery morphology, spina bifida occulta, abnormal otic vesicle development, abnormal presphenoid bone morphology, abnormal basisphenoid bone morphology, aortic arch coarctation, cleft secondary palate, abnormal palatine bone horizontal plate morphology, gonial bone hypoplasia, perinatal lethality, complete penetrance, small vertebral body, rib fusion, short vertebral body, malleus hypoplasia, atelectasis, embryonic lethality during organogenesis, incomplete penetrance, abnormal third pharyngeal arch artery morphology, abnormal bone ossification, interrupted aortic arch, abnormal alisphenoid bone morphology, abnormal craniofacial bone morphology, abnormal vertebral body morphology, absent soft palate, abnormal vertebral body morphology, abnormal sphenoid bone morphology | Foxc2 | tm1Miu | 2169410 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9409679 PMID:10364424 |
2024-01-30 12:21:15 | 0 | ||
|
Map2k4tm1Pngr/Map2k4tm1Pngr Resource Report The record is no longer available at this source. |
RRID:MGI:2167066 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | embryonic lethality during organogenesis, complete penetrance, anemia, abnormal liver development | Map2k4 | tm1Pngr | 2167066 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9876179 | 2024-01-30 12:21:16 | 0 | ||
|
Gab1tm1Wbm/Gab1tm1Wbm Resource Report The record is no longer available at this source. |
RRID:MGI:2177557 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal muscle precursor cell migration, abnormal keratinocyte physiology, thin placenta labyrinth, fetal growth retardation, lethality throughout fetal growth and development, complete penetrance, hypaxial muscle hypoplasia, decreased trophoblast giant cell number, abnormal placenta vasculature, abnormal placenta labyrinth morphology, abnormal diaphragm development, abnormal hair follicle development, disorganized placental labyrinth, decreased liver weight, thin epidermis | Gab1 | tm1Wbm | 2177557 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10995442 | 2024-01-30 12:21:09 | 0 | ||
|
Gabrg2tm1Lusc/Gabrg2tm1Lusc Resource Report The record is no longer available at this source. |
RRID:MGI:2177609 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | limb grasping, impaired righting response, abnormal gait, postnatal lethality, complete penetrance, hyperactivity, nervous system phenotype | Gabrg2 | tm1Lusc | 2177609 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:7644489 | 2024-01-30 12:21:09 | 0 | ||
|
Cftrtm2Hgu/Cftrtm2Hgu Resource Report The record is no longer available at this source. |
RRID:MGI:2177545 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | craniofacial phenotype, reproductive system phenotype, abnormal digestive system physiology, abnormal respiratory system physiology, abnormal intestinal goblet cell morphology | Cftr | tm2Hgu | 2177545 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11823443 | 2024-01-30 12:21:09 | 0 | ||
|
Grm1tm1Crpl/Grm1tm1Crpl Resource Report The record is no longer available at this source. |
RRID:MGI:2176844 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | tremors, ataxia, reduced long term potentiation, decreased exploration in new environment, reduced long term depression, abnormal spatial learning, impaired righting response | Grm1 | tm1Crpl | 2176844 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:7969468 | 2024-01-30 12:21:10 | 0 | ||
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Atrtm1Akl/Atrtm1Akl Resource Report The record is no longer available at this source. |
RRID:MGI:2176609 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | embryonic lethality between implantation and somite formation, complete penetrance | Atr | tm1Akl | 2176609 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10801416 | 2024-01-30 12:21:10 | 0 | ||
|
Bcl2a1atm1Sen/Bcl2a1atm1Sen Resource Report The record is no longer available at this source. |
RRID:MGI:2176731 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | focal hair loss, abnormal neutrophil physiology | Bcl2a1a | tm1Sen | 2176731 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9841913 | 2024-01-30 12:21:10 | 0 | ||
|
Atrtm1Akl/Atr+ Resource Report The record is no longer available at this source. |
RRID:MGI:2176610 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | neoplasm | Atr | tm1Akl | 2176610 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10801416 | 2024-01-30 12:21:10 | 0 | ||
|
Bcl2tm1Dlo/Bcl2tm1Dlo Resource Report The record is no longer available at this source. |
RRID:MGI:2176707 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | expanded mesangial matrix, decreased body size, dilated renal tubules, decreased renal glomerulus number, decreased body weight, postnatal lethality, incomplete penetrance, decreased CD8-positive, alpha-beta T cell number, decreased mature B cell number, abnormal kidney morphology, podocyte hypertrophy, renal glomerular synechia, increased renal glomerulus apoptosis, decreased glomerular capsule space, abnormal glomerular capillary endothelium morphology, small kidney, renal tubule hypertrophy, small kidney, renal glomerulus hypertrophy, podocyte foot process effacement, mesangiolysis, increased kidney apoptosis, glomerulosclerosis, dilated renal tubules, abnormal podocyte morphology, abnormal kidney cortex morphology, abnormal kidney blood vessel morphology, abnormal glomerular capsule parietal layer morphology, decreased kidney weight, decreased nephron number, kidney failure, decreased renal glomerulus number, kidney degeneration, abnormal T cell differentiation, decreased lymphocyte cell number, decreased thymocyte number, abnormal ureteric bud elongation, abnormal kidney corticomedullary boundary morphology, abnormal kidney development, abnormal nephrogenic zone morphology, abnormal renal glomerulus morphology, renal tubule hypertrophy, decreased nephron number, decreased renal glomerulus number, dilated renal tubules, impaired branching involved in ureteric bud morphogenesis, increased kidney apoptosis, renal glomerulus hypertrophy, renal hypoplasia, small kidney, small ureteric bud, decreased pre-B cell number, abnormal coat/hair pigmentation, abnormal kidney cortex morphology, abnormal renal tubule epithelium morphology, pale kidney, abnormal kidney medulla morphology, round snout, polycystic kidney, small ears | Bcl2 | tm1Dlo | 2176707 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9794553 PMID:8623928 PMID:8170972 |
2024-01-30 12:21:10 | 0 | ||
|
Fgfr2tm3Dsn/Fgfr2tm3Dsn Resource Report The record is no longer available at this source. |
RRID:MGI:2176484 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal hair follicle morphology, thin epidermis, abnormal epidermis stratum basale morphology, abnormal epidermal layer morphology, decreased hair follicle number, abnormal vibrissa number, abnormal keratinocyte morphology, abnormal hair follicle development, ventricular hypoplasia, abnormal left posterior bundle morphology, absent eyelids, decreased fetal size, overriding aortic valve, absent lungs, delayed intramembranous bone ossification, cleft palate, abnormal pancreas development, abnormal adrenal gland development, thin skin, abnormal conotruncal ridge morphology, double outlet right ventricle, atrium hypoplasia, abnormal trabecula carnea morphology, absent pulmonary vein, abnormal pulmonary circulation, absent thyroid gland, abnormal kidney development, absent adenohypophysis, small otic capsule, abnormal stomach glandular region morphology, absent teeth, abnormal skin morphology, decreased nephron number, abnormal heart ventricle morphology, perinatal lethality, complete penetrance, absent pulmonary artery, conotruncal ridge hypoplasia, abnormal interventricular groove morphology, muscular ventricular septal defect, perimembraneous ventricular septal defect, abnormal truncus arteriosus septation, curly tail, abnormal heart development, thin ventricular wall, absent limbs, abnormal hair follicle morphology, small kidney, caudal vertebral fusion, abnormal thymus development, abnormal otic vesicle development, abnormal scapula morphology, abnormal pelvic girdle bone morphology, abnormal apical ectodermal ridge morphology, abnormal salivary gland morphology, hypospadia, abnormal urethra morphology, thin skin | Fgfr2 | tm3Dsn | 2176484 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:16687131 PMID:14530295 PMID:11180951 PMID:15843416 |
2024-01-30 12:21:10 | 0 | ||
|
Tgfatm1Unc/Tgfatm1Unc; Aregtm1Dle/Aregtm1Dle; Egftm1Dle/Egftm1Dle Resource Report The record is no longer available at this source. |
RRID:MGI:2176534 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | corneal opacity, hypolactation, dermatitis, microphthalmia, spontaneous skin ulceration, waved hair, abnormal branching of the mammary ductal tree, abnormal mammary gland growth during pregnancy, eyelids open at birth, postnatal growth retardation, curly vibrissae, alopecia, weight loss, abnormal intestinal goblet cell morphology, abnormal ileum morphology, abnormal small intestine crypts of Lieberkuhn morphology, decreased body weight, duodenal lesions, abnormal small intestine morphology | Areg, Tgfa, Egf | tm1Dle, tm1Unc | 2176534 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11438495 PMID:10331984 |
2024-01-30 12:21:10 | 0 | ||
|
Erbb2tm1Cbm/Erbb2tm1Cbm Resource Report The record is no longer available at this source. |
RRID:MGI:2175861 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal neural crest cell migration, decreased Schwann cell precursor number, abnormal sympathetic ganglion morphology, absent trabeculae carneae, embryonic lethality, complete penetrance, decreased neuronal precursor cell number, abnormal cranial ganglia morphology | Erbb2 | tm1Cbm | 2175861 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9637684 | 2024-01-30 12:21:10 | 0 | ||
|
Gfaptm1Ldtk/Gfaptm1Ldtk Resource Report The record is no longer available at this source. |
RRID:MGI:2677143 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal blood-brain barrier function, non-obstructive hydrocephaly, decreased corpus callosum size, abnormal myelination, abnormal astrocyte morphology, abnormal brain white matter morphology, abnormal blood vessel morphology, abnormal oligodendrocyte morphology, abnormal oligodendrocyte physiology | Gfap | tm1Ldtk | 2677143 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:8893019 | 2024-01-30 12:20:53 | 0 | ||
|
Canxtm1Den/Canxtm1Den Resource Report The record is no longer available at this source. |
RRID:MGI:2677259 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | ataxia, positive geotaxis, novel environmental response-related retropulsion, decreased body size, postnatal lethality, incomplete penetrance, abnormal nervous system morphology | Canx | tm1Den | 2677259 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12370287 | 2024-01-30 12:20:53 | 0 | ||
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Synpotm1Mndl/Synpotm1Mndl Resource Report The record is no longer available at this source. |
RRID:MGI:2675736 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased anxiety-related response, renal/urinary system phenotype, abnormal brain morphology, abnormal telencephalon development, reduced long term potentiation, hypoactivity, abnormal spatial learning | Synpo | tm1Mndl | 2675736 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:12928494 | 2024-01-30 12:20:54 | 0 | ||
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Mpgtm1Lds/Mpgtm1Lds Resource Report The record is no longer available at this source. |
RRID:MGI:2675731 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | increased circulating glucose level, decreased susceptibility to autoimmune diabetes, autoimmune response, small pancreatic islets, increased apoptosis | Mpg | tm1Lds | 2675731 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:17098815 | 2024-01-30 12:20:54 | 0 |
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