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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.

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  • Background:involves: 129p2/olahsd * c57bl/6 (facet)

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2,505 Results - per page

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Organism Name Proper Citation Species Synonyms Notes Phenotype Affected Gene Genomic Alteration Catalog Number Background Database Database Abbreviation Availability Source References Alternate IDs Record Last Update Mentions Count
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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