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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Foxn1nu/Foxn1nu; Tg(Foxn1)G2Hon Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2174844 | Mus musculus | Allele Detail: Spontaneous, Transgenic This is a legacy resource. | hairless, infertility | Foxn1 | Tg(Foxn1)G2Hon, nu | 2174844 | involves: CD-1 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:8671685 | 2024-01-30 12:21:14 | 1 | ||
|
Tg(Foxn1)E1Hon; Foxn1nu/Foxn1nu Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2174843 | Mus musculus | Allele Detail: Transgenic, Spontaneous This is a legacy resource. | athymia, hairless | Foxn1 | nu, Tg(Foxn1)E1Hon | 2174843 | involves: CD-1 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:8671685 | 2024-01-30 12:21:41 | 1 | ||
|
Tcirg1oc/Tcirg1oc Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2174761 | Mus musculus | Allele Detail: Spontaneous This is a legacy resource. | delayed tooth eruption, circling, extramedullary hematopoiesis, delayed tooth eruption, increased long bone epiphyseal plate size, increased long bone epiphyseal plate size, abnormal long bone hypertrophic chondrocyte zone, failure of bone resorption, increased width of hypertrophic chondrocyte zone, abnormal long bone metaphysis morphology, decreased body size, circling, abnormal long bone metaphysis morphology, abnormal incisor morphology, weight loss, osteopetrosis, increased megakaryocyte cell number, postnatal lethality, complete penetrance, abnormal predentin morphology, abnormal osteoclast morphology, abnormal thyroid gland morphology, decreased body size, decreased body weight, decreased insulin secretion, decreased circulating insulin level | Tcirg1 | oc | 2174761 | B6C3Fe a/a-Tcirg1 |
MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:3976544 PMID:3998439 PMID:17046993 PMID:10709991 |
2024-01-30 12:21:14 | 1 | ||
|
Phox2btm1Jbr/Phox2btm1Jbr Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2172761 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | abnormal cranial ganglia morphology, abnormal area postrema morphology, abnormal carotid body morphology, abnormal medulla oblongata morphology, abnormal motor neuron morphology, abnormal cranial nerve morphology, absent trigeminal nerve, abnormal vagus nerve morphology, absent facial nerve, abnormal vagus ganglion morphology, abnormal sympathetic ganglion morphology, abnormal parasympathetic ganglion morphology, abnormal noradrenaline level, abnormal glossopharyngeal ganglion morphology, abnormal geniculate ganglion morphology, abnormal enteric ganglia morphology, abnormal noradrenaline level, embryonic lethality during organogenesis, incomplete penetrance, lethality throughout fetal growth and development, complete penetrance, vasculature congestion, abnormal locus ceruleus morphology, abnormal autonomic nervous system morphology, abnormal petrosal ganglion morphology, abnormal nodose ganglion morphology, abnormal cranial ganglia morphology, abnormal motor neuron morphology, abnormal geniculate ganglion morphology | Phox2b | tm1Jbr | 2172761 | Not Specified | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10704382 PMID:10360575 PMID:14627719 PMID:10736201 |
2024-01-30 12:21:14 | 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 |
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 |
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 | 2024-01-30 12:21:08 | 1 | ||
|
Foxa2tm1Khk/Foxa2tm1Khk Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2177357 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | no abnormal phenotype detected | Foxa2 | tm1Khk | 2177357 | involves: 129P2/OlaHsd * CD-1 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:10866673 | 2024-01-30 12:21:09 | 1 | ||
|
Tfamtm1.1Lrsn/Tfamtm1.1Lrsn Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2177633 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | increased apoptosis, disorganized mitochondrial cristae, absent optic nerve, decreased body size, embryonic lethality during organogenesis, complete penetrance, increased mitochondria size, abnormal mitochondrial ATP synthesis coupled electron transport, abnormal nervous system physiology, abnormal heart development, decreased mitochondrial DNA content, abnormal somite development | Tfam | tm1.1Lrsn | 2177633 | involves: 129S1/Sv * 129X1/SvJ * FVB/N | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11259653 PMID:9500544 |
2024-01-30 12:21:09 | 1 | ||
|
Tfamtm1Lrsn/Tfamtm1Lrsn; Tg(Ckmm-cre)1Lrsn Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2177634 | Mus musculus | Allele Detail: Transgenic, Targeted This is a legacy resource. | postnatal growth retardation, increased physiological sensitivity to xenobiotic, dilated cardiomyopathy, abnormal respiratory electron transport chain, abnormal enzyme/coenzyme level, increased cardiomyocyte apoptosis, increased glutathione peroxidase activity, postnatal lethality, complete penetrance, bradykinesia, enlarged heart, dilated heart left ventricle, increased heart weight, abnormal blood flow velocity, abnormal cardiovascular system physiology | Tfam, Tg(Ckmm-cre)1Lrsn | tm1Lrsn, Tg(Ckmm-cre)1Lrsn | 2177634 | involves: 129S1/Sv * 129X1/SvJ | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9916807 PMID:11259653 |
2024-01-30 12:21:09 | 1 | ||
|
Hexbtm1Rlp/Hexbtm1Rlp Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2177468 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | weight loss, tremors, premature death, bradykinesia, impaired righting response, premature death, impaired coordination, abnormal motor capabilities/coordination/movement, abnormal gait, abnormal neuron morphology, muscular atrophy, abnormal hepatocyte morphology, abnormal proximal convoluted tubule morphology, abnormal liver morphology | Hexb | tm1Rlp | 2177468 | involves: 129S4/SvJae * C57BL/6 | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:23028353 PMID:7550345 PMID:10021458 |
2024-01-30 12:21:52 | 1 | ||
|
Sgcatm1Kcam/Sgcatm1Kcam Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2176866 | Mus musculus | Allele Detail: Targeted This is a legacy resource. | increased circulating creatine kinase level, centrally nucleated skeletal muscle fibers, increased extensor digitorum longus weight, heart inflammation, abnormal muscle contractility, muscle phenotype, abnormal skeletal muscle fiber morphology, calcified muscle, cardiac fibrosis, cardiac muscle necrosis, cardiomyopathy, dystrophic muscle, abnormal muscle fiber morphology, increased circulating creatine kinase level, abnormal sarcolemma morphology, abnormal circulating pyruvate kinase level, increased soleus weight | Sgca | tm1Kcam | 2176866 | involves: 129S1/Sv * 129X1/SvJ | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9744877 PMID:21890494 PMID:18252746 PMID:18252745 |
2024-01-30 12:21:09 | 1 | ||
|
Tg(Syn1-cre)671Jxm; Nf1tm1Par/Nf1tm1Par Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2176767 | Mus musculus | Allele Detail: Transgenic, Targeted This is a legacy resource. | decreased body weight, abnormal learning/memory/conditioning, neoplasm, postnatal growth retardation, decreased forebrain size, thin cerebral cortex, abnormal cerebral cortex morphology, astrocytosis | Tg(Syn1-cre)671Jxm, Nf1 | Tg(Syn1-cre)671Jxm, tm1Par | 2176767 | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:11297510 | 2024-01-30 12:21:10 | 1 | ||
|
Gt(ROSA)26Sor/Gt(ROSA)26Sor Resource Report 1+ mentions The record is no longer available at this source. |
RRID:MGI:2176738 | Mus musculus | Allele Detail: Gene trapped This is a legacy resource. | no abnormal phenotype detected | Gt(ROSA)26Sor | Gt(ROSA)26Sor | 2176738 | involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6J | MGI, Mouse Genome Informatics MGI | MGI | Availability unknown check source stock center | PMID:9108056 | 2024-01-30 12:21:10 | 1 | ||
|
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 |
2024-01-30 12:20:59 | 1 | ||
|
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 | 2024-01-30 12:20:59 | 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 | 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 | 2024-01-30 12:21:01 | 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 | 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 | 2024-01-30 12:21:02 | 1 |
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