Searching across hundreds of databases

Our searching services are busy right now. Your search will reload in five seconds.

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes
on page 1 showing 20 out of 1,659 results from 1 sources

Cite this (MGI Cat# 5317173, RRID:MGI:5317173)

Source Database: MGI, catalog # 5317173
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * SJL
Affected Genes: Gjc1, Tg(Nes-cre)1Kln
Genomic Alteration: tm1.1(Gjd2)Kwi; Tg(Nes-cre)1Kln
Availability: Availability unknown check source stock center
Reference: PMID:20930146
Notes: nervous system phenotype, vision/eye phenotype Allele Detail: Targeted, Transgenic

  • From Current Category

Cite this (MGI Cat# 5000268, RRID:MGI:5000268)

Source Database: MGI, catalog # 5000268
Genetic Background: C57BL/6J-Ticam1
Affected Genes: Ticam1
Genomic Alteration: Lps2
Availability: Availability unknown check source stock center
Reference: PMID:18981228, PMID:18713975, PMID:20855887, PMID:19825364, PMID:18209032
Notes: abnormal retinal progenitor cell morphology, nervous system phenotype, abnormal enterocyte physiology, decreased susceptibility to induced colitis, immune system phenotype, abnormal cytokine secretion, decreased interleukin-6 secretion, abnormal circulating tumor necrosis factor level, abnormal postnatal growth/weight/body size, decreased susceptibility to hepatic steatosis Allele Detail: Chemically induced (ENU)

  • From Current Category

Cite this (MGI Cat# 3759808, RRID:MGI:3759808)

Source Database: MGI, catalog # 3759808
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Affected Genes: Mapk1
Genomic Alteration: tm1Kuta
Availability: Availability unknown check source stock center
Reference: PMID:17913910
Notes: abnormal contextual conditioning behavior, abnormal cued conditioning behavior, abnormal spatial learning, behavior/neurological phenotype, nervous system phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3802986, RRID:MGI:3802986)

Source Database: MGI, catalog # 3802986
Genetic Background: B6.Cg-Adcy1 Adcy1 Tg(Emx1-cre)3Ito
Affected Genes: Adcy1
Genomic Alteration: Tg(Emx1-cre)3Ito; tm1.1Ito; tm1Ito
Availability: Availability unknown check source stock center
Reference: PMID:18524897
Notes: abnormal barrel cortex morphology, abnormal miniature excitatory postsynaptic currents, nervous system phenotype, reduced long term potentiation Allele Detail: Targeted, Transgenic

  • From Current Category

Cite this (MGI Cat# 4833965, RRID:MGI:4833965)

Source Database: MGI, catalog # 4833965
Genetic Background: involves: C57BL/6 * C57BL/6J * DBA/2
Affected Genes: Tnfrsf1a
Genomic Alteration: tm1Imx; Tg(Thy1-APP)3Somm
Availability: Availability unknown check source stock center
Reference: PMID:17724122
Notes: amyloid beta deposits, behavior/neurological phenotype, cerebral amyloid angiopathy, microgliosis, nervous system phenotype Allele Detail: Targeted, Transgenic

  • From Current Category

Cite this (MGI Cat# 3760750, RRID:MGI:3760750)

Source Database: MGI, catalog # 3760750
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Affected Genes: Gucy2d, Sema3c
Genomic Alteration: tm1.1Jra; tm1Mom
Availability: Availability unknown check source stock center
Reference: PMID:17942483
Notes: nervous system phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3613509, RRID:MGI:3613509)

Source Database: MGI, catalog # 3613509
Genetic Background: involves: 129S1/SvImJ * C57BL/6J
Affected Genes: Mobp
Genomic Alteration: tm1Irg
Availability: Availability unknown check source stock center
Reference: PMID:12203392
Notes: nervous system phenotype, behavior/neurological phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3798665, RRID:MGI:3798665)

Source Database: MGI, catalog # 3798665
Genetic Background: involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m musculus
Affected Genes: Dmd, Utrn
Genomic Alteration: mdx-3Cv; tm1Ked
Availability: Availability unknown check source stock center
Reference: PMID:10204788
Notes: abnormal skeletal muscle morphology, liver/biliary system phenotype, nervous system phenotype, renal/urinary system phenotype, reproductive system phenotype, respiratory system phenotype Allele Detail: Chemically induced (ENU), Targeted

  • From Current Category

Cite this (MGI Cat# 3720209, RRID:MGI:3720209)

Source Database: MGI, catalog # 3720209
Genetic Background: involves: FVB
Affected Genes:
Genomic Alteration: Tg(Thy1-MAPT)1Vln
Availability: Availability unknown check source stock center
Reference: PMID:11007782, PMID:10595944
Notes: abnormal cell cytoskeleton morphology, abnormal axon morphology, abnormal axon morphology, abnormal locomotor activation, abnormal neuron morphology, abnormal postural reflex, skeletal muscle fiber atrophy, astrocytosis, axon degeneration, decreased skeletal muscle mass, impaired coordination, impaired coordination, limb grasping, muscle weakness, muscular atrophy, nervous system phenotype, decreased body weight, impaired righting response, muscular atrophy, tau protein deposits Allele Detail: Transgenic

  • From Current Category

Cite this (MGI Cat# 4867727, RRID:MGI:4867727)

Source Database: MGI, catalog # 4867727
Genetic Background: 129S/SvEv-Mapk8ip2
Affected Genes: Mapk8ip2
Genomic Alteration: tm1.1Gol
Availability: Availability unknown check source stock center
Reference: PMID:21048139
Notes: reduced AMPA-mediated synaptic currents, abnormal Purkinje cell dendrite morphology, abnormal Purkinje cell morphology, abnormal excitatory postsynaptic currents, abnormal miniature excitatory postsynaptic currents, abnormal social investigation, behavior/neurological phenotype, decreased anxiety-related response, decreased exploration in new environment, decreased grip strength, decreased synaptic glutamate release, enhanced NMDA-mediated synaptic currents, impaired coordination, nervous system phenotype, reduced fertility, taste/olfaction phenotype, thin cerebellar molecular layer, vision/eye phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 5824114, RRID:MGI:5824114)

Source Database: MGI, catalog # 5824114
Genetic Background: involves: 129S/SvEv * C3H * C57BL/6 * C57BL/6N
Affected Genes: Fus
Genomic Alteration: Tg(UBC-cre/ERT2)1Ejb; tm1c(EUCOMM)Wtsi; tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:26842965
Notes: nervous system phenotype Allele Detail: Transgenic, Targeted

  • From Current Category

Cite this (MGI Cat# 5527535, RRID:MGI:5527535)

Source Database: MGI, catalog # 5527535
Genetic Background: involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * FVB/N * SJL
Affected Genes: Dmrta2
Genomic Alteration: tm1.2Fuma
Availability: Availability unknown check source stock center
Reference: PMID:23056351
Notes: abnormal cerebral cortex morphology, abnormal neuronal precursor proliferation, absent hippocampus, decreased neuron number, decreased neuronal precursor cell number, nervous system phenotype, small olfactory bulb, telencephalon hypoplasia Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 4836986, RRID:MGI:4836986)

Source Database: MGI, catalog # 4836986
Genetic Background: involves: 129S/SvEv * 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6
Affected Genes: Smn1
Genomic Alteration: tm1.1Dscd; tm1Msd
Availability: Availability unknown check source stock center
Reference: PMID:20705738
Notes: decreased grip strength, decreased vertical activity, hypoactivity, nervous system phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3720601, RRID:MGI:3720601)

Source Database: MGI, catalog # 3720601
Genetic Background: involves: BALB/c
Affected Genes: Reln
Genomic Alteration: rl
Availability: Availability unknown check source stock center
Reference: PMID:10876649
Notes: Purkinje cell degeneration, decreased Purkinje cell number, small cerebellum, nervous system phenotype Allele Detail: Spontaneous

  • From Current Category

Cite this (MGI Cat# 5432789, RRID:MGI:5432789)

Source Database: MGI, catalog # 5432789
Genetic Background: involves: 129S6/SvEvTac * C57BL/6NTac
Affected Genes: Cntf
Genomic Alteration: tm1Vlcg
Availability: Availability unknown check source stock center
Reference: PMID:18305256
Notes: abnormal neuron proliferation, decreased neuronal precursor cell number, nervous system phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3713514, RRID:MGI:3713514)

Source Database: MGI, catalog # 3713514
Genetic Background: B6.Cg-Tyr Sept5
Affected Genes: Sept5
Genomic Alteration: tm1Bld
Availability: Availability unknown check source stock center
Reference: PMID:16684884
Notes: nervous system phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3764503, RRID:MGI:3764503)

Source Database: MGI, catalog # 3764503
Genetic Background: involves: 129P2/OlaHsd * BALB/c
Affected Genes: Camk2a
Genomic Alteration: tm1Sva
Availability: Availability unknown check source stock center
Reference: PMID:1378648
Notes: decreased anxiety-related response, decreased paired-pulse facilitation, nervous system phenotype, reduced long term potentiation Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 2450119, RRID:MGI:2450119)

Source Database: MGI, catalog # 2450119
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ugt8a
Genomic Alteration: tm1Pop
Availability: Availability unknown check source stock center
Reference: PMID:8706126, PMID:9464989, PMID:10601330
Notes: abnormal head movements, abnormal lipid level, abnormal myelination, abnormal nerve conduction, abnormal nerve conduction, ataxia, decreased body weight, hindlimb paralysis, immune system phenotype, nervous system phenotype, premature death, tremors Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3718910, RRID:MGI:3718910)

Source Database: MGI, catalog # 3718910
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: App
Genomic Alteration: tm1Umu
Availability: Availability unknown check source stock center
Reference: PMID:17634375
Notes: behavior/neurological phenotype, growth/size/body region phenotype, nervous system phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3818484, RRID:MGI:3818484)

Source Database: MGI, catalog # 3818484
Genetic Background: B6.129P2-Tyrobp
Affected Genes: Tyrobp
Genomic Alteration: tm1.1Viv
Availability: Availability unknown check source stock center
Reference: PMID:15632019, PMID:15601948, PMID:17611620
Notes: abnormal excitatory postsynaptic currents, enhanced long term potentiation, increased physiological sensitivity to xenobiotic, abnormal axon morphology, abnormal bone ossification, abnormal bone remodeling, increased trabecular bone volume, abnormal microglial cell morphology, abnormal myelination, abnormal myelopoiesis, abnormal osteoclast physiology, decreased bone resorption, decreased bone resorption, increased bone mineral density, increased bone mass, increased bone mass, nervous system phenotype, osteopetrosis, abnormal bone remodeling, abnormal osteoclast physiology, increased bone mineral content, increased bone trabecula number Allele Detail: Targeted

  • From Current Category

  1. Resource Identification Portal Resources

    Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that RRID has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on RRID then you can log in from here to get additional features in RRID such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Save Your Search

    You can save any searches you perform for quick access to later from here.

  6. Query Expansion

    We recognized your search term and included synonyms and inferred terms along side your term to help get the data you are looking for.

  7. Collections

    If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  8. Sources

    Here are the sources that were queried against in your search that you can investigate further.

  9. Categories

    Here are the categories present within RRID that you can filter your data on

  10. Subcategories

    Here are the subcategories present within this category that you can filter your data on

  11. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.

X