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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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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 | ||
|
Nrg1tm2Cbm/Nrg1tm2Cbm Resource Report The record is no longer available at this source. |
RRID:MGI:2175172 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased Schwann cell precursor number, enlarged pericardium, embryonic lethality during organogenesis, complete penetrance, abnormal cranial nerve morphology, irregular heartbeat, absent trigeminal nerve, enlarged heart, failure of atrioventricular cushion closure, small petrosal ganglion, small nodose ganglion, abnormal cranial ganglia morphology, abnormal superior vagus ganglion morphology, trabecula carnea hypoplasia, abnormal mandibular nerve innervation pattern | Nrg1 | tm2Cbm | 2175172 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:7477375 | 2024-01-30 12:21:13 | 0 | ||
|
Nrg1tm1Cbm/Nrg1tm1Cbm Resource Report The record is no longer available at this source. |
RRID:MGI:2175167 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased Schwann cell precursor number, embryonic lethality during organogenesis, complete penetrance, decreased radial glial cell number, small petrosal ganglion, abnormal cranial ganglia morphology, abnormal cranial nerve morphology, abnormal superior vagus ganglion morphology, absent trigeminal nerve, abnormal mandibular nerve innervation pattern, enlarged heart, absent oligodendrocytes, trabecula carnea hypoplasia, irregular heartbeat, enlarged pericardium, small nodose ganglion, failure of atrioventricular cushion closure | Nrg1 | tm1Cbm | 2175167 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:7477375 PMID:9892702 PMID:12649319 |
2024-01-30 12:21:13 | 0 | ||
|
Fgf6tm1Ffi/Fgf6tm1Ffi Resource Report The record is no longer available at this source. |
RRID:MGI:2175022 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | no abnormal phenotype detected | Fgf6 | tm1Ffi | 2175022 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9303352 | 2024-01-30 12:21:13 | 0 | ||
|
Clcnkatm1Suc/Clcnkatm1Suc Resource Report The record is no longer available at this source. |
RRID:MGI:2174943 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased urine osmolality, polyuria | Clcnka | tm1Suc | 2174943 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9916798 | 2024-01-30 12:21:13 | 0 | ||
|
Ptger3tm1Sna/Ptger3tm1Sna Resource Report The record is no longer available at this source. |
RRID:MGI:2175005 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | homeostasis/metabolism phenotype, impaired febrile response, mortality/aging | Ptger3 | tm1Sna | 2175005 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9751056 PMID:11966527 |
2024-01-30 12:21:13 | 0 | ||
|
Ptger1tm1Sna/Ptger1tm1Sna Resource Report The record is no longer available at this source. |
RRID:MGI:2175004 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal physiological response to xenobiotic, mortality/aging, homeostasis/metabolism phenotype, increased physiological sensitivity to xenobiotic | Ptger1 | tm1Sna | 2175004 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9751056 PMID:11966527 |
2024-01-30 12:21:13 | 0 | ||
|
Ptgirtm1Sna/Ptgirtm1Sna Resource Report The record is no longer available at this source. |
RRID:MGI:2175008 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal platelet physiology, abnormal thrombosis, abnormal blood coagulation, abnormal thrombosis, mortality/aging, cardiovascular system phenotype, prenatal lethality, incomplete penetrance, decreased acute inflammation, abnormal blood vessel physiology, vascular restenosis, decreased prostaglandin level, increased chemical nociceptive threshold, abnormal thromboxane level, abnormal cardiovascular system physiology | Ptgir | tm1Sna | 2175008 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11964481 PMID:16614756 PMID:9262402 |
2024-01-30 12:21:13 | 0 | ||
|
Hesx1tm1Icar/Hesx1tm1Icar Resource Report The record is no longer available at this source. |
RRID:MGI:2175062 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | absent otic vesicle, decreased forebrain size, absent hippocampal commissure, abnormal midbrain-hindbrain boundary development, absent pituitary infundibular stalk, absent Rathke's pouch, abnormal septum pellucidum morphology, microphthalmia, enophthalmos, olfactory bulb hypoplasia, abnormal telencephalon morphology, absent corpus callosum, small vomeronasal organ, anophthalmia, abnormal eye morphology, abnormal telencephalon morphology, absent anterior commissure, abnormal olfactory epithelium morphology, abnormal nasal cavity morphology, abnormal optic vesicle formation, abnormal nasal pit morphology, abnormal hypothalamus morphology, decreased embryonic neuroepithelium thickness, bifurcated Rathke's pouch, abnormal optic cup morphology, abnormal craniofacial morphology, short snout, microcephaly, abnormal telencephalon development, decreased forebrain size, abnormal nasal placode morphology, small embryonic telencephalon, small adenohypophysis, abnormal forebrain development, abnormal frontonasal prominence morphology, anophthalmia, small embryonic telencephalon, postnatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance | Hesx1 | tm1Icar | 2175062 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9620767 PMID:17360769 PMID:19093031 |
2024-01-30 12:21:13 | 0 | ||
|
Nos3tm1Unc/Nos3tm1Unc Resource Report The record is no longer available at this source. |
RRID:MGI:2174981 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | increased circulating renin level, abnormal heart weight, abnormal cardiovascular system morphology, increased mean systemic arterial blood pressure, abnormal heart right ventricle pressure, abnormal cardiovascular system physiology, decreased sensitivity to induced morbidity/mortality, decreased body weight, decreased vascular permeability, increased systemic arterial blood pressure, abnormal pulmonary artery morphology, decreased body weight, decreased body temperature, decreased heart rate, immune system phenotype | Nos3 | tm1Unc | 2174981 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:15821017 PMID:16886062 PMID:8917564 |
2024-01-30 12:21:13 | 0 | ||
|
Grin1tm1Blt/Grin1tm1Blt Resource Report The record is no longer available at this source. |
RRID:MGI:2175048 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | decreased susceptibility to pharmacologically induced seizures, abnormal locomotor behavior, abnormal nervous system physiology, increased startle reflex, abnormal spatial learning, impaired coordination, reduced long term potentiation | Grin1 | tm1Blt | 2175048 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10818139 | 2024-01-30 12:21:13 | 0 | ||
|
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 | ||
|
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 | ||
|
Hhextm1Rbe/Hhextm1Rbe Resource Report The record is no longer available at this source. |
RRID:MGI:3707078 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | rostral body truncation, lethality throughout fetal growth and development, complete penetrance, embryonic growth retardation, abnormal telencephalon development, abnormal thyroid gland development, absent nasal placodes, abnormal optic stalk morphology, anophthalmia, absent forebrain, abnormal pericardial cavity morphology, decreased forebrain size, small embryonic telencephalon, absent liver, embryonic lethality during organogenesis, incomplete penetrance, abnormal nasal placode morphology, abnormal medial ganglionic eminence morphology, abnormal forebrain development, abnormal anterior definitive endoderm morphology, absent Rathke's pouch, abnormal hepatic diverticulum morphology, abnormal hepatoblast migration, abnormal first pharyngeal arch morphology, absent embryonic telencephalon, fused first pharyngeal arch, abnormal thyroid gland morphology, abnormal optic vesicle formation | Hhex | tm1Rbe | 3707078 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10804184 | 2024-01-30 12:19:44 | 0 | ||
|
Myd88tm1Aki/Myd88tm1Aki Resource Report The record is no longer available at this source. |
RRID:MGI:3707236 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal cytokine secretion, abnormal macrophage physiology, decreased interleukin-6 secretion, decreased IgG3 level, decreased IgG2b level, abnormal chemokine secretion, abnormal dendritic cell physiology, decreased IgG level, abnormal macrophage physiology, immune system phenotype, decreased incidence of tumors by chemical induction, decreased interleukin-1 beta secretion | Myd88 | tm1Aki | 3707236 | involves: 129P2/OlaHsd * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:17525287 PMID:20526283 PMID:18776906 PMID:17118979 PMID:17486093 PMID:18492657 PMID:18256672 PMID:16407889 |
2024-01-30 12:19:44 | 0 |
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