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on page 1 showing 20 out of 2,861 results from 1 sources

Cite this (RGD Cat# 10026, RRID:RGD_10026)

Source Database: RGD, catalog # 10026
Genetic Background: inbred strain
Affected Genes:
Genomic Alteration:
Availability: live
Reference:
Notes: decreased body weight, decreased systemic arterial blood pressure To N 1964 at F18+? from Maas. Developed by Broadhurst, 1954, from a commercial stock, with selection for low defecation response in an open field. A number of parallel sublines are in existence; these differ at least at the agouti and the major histocompatibility loci. NIH Animal Genetic Resource

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Cite this (MGI Cat# 4834522, RRID:MGI:4834522)

Source Database: MGI, catalog # 4834522
Genetic Background: involves: 129S6/SvEvTac * C57BL/6N
Affected Genes: Fkrp
Genomic Alteration: tm1Itl
Availability: Availability unknown check source stock center
Reference: PMID:20675713
Notes: abnormal brain morphology, abnormal brainstem morphology, abnormal cerebellar foliation, abnormal dentate gyrus morphology, abnormal eye size, abnormal neuronal migration, abnormal optic disc morphology, parietal bossing, abnormal retina inner limiting membrane morphology, abnormal retinal ganglion layer morphology, abnormal skeletal muscle fiber morphology, abnormal stratification in cerebral cortex, centrally nucleated skeletal muscle fibers, corneal opacity, decreased birth body size, decreased body weight, dilated lateral ventricles, domed cranium, dystrophic muscle, homeostasis/metabolism phenotype, hydroencephaly, increased circulating alanine transaminase level, increased circulating creatine kinase level, increased variability of skeletal muscle fiber size, limb grasping, muscle weakness, neonatal lethality, incomplete penetrance, optic nerve hypoplasia, postnatal lethality, incomplete penetrance, skeletal muscle fiber degeneration, skeletal muscle fiber necrosis, skeletal muscle fibrosis, thin retinal inner nuclear layer, thin retinal outer nuclear layer Allele Detail: Targeted

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Cite this (MGI Cat# 3848827, RRID:MGI:3848827)

Source Database: MGI, catalog # 3848827
Genetic Background: involves: 129/Sv
Affected Genes: Rasgrf1
Genomic Alteration: tm1Toc
Availability: Availability unknown check source stock center
Reference: PMID:9603515
Notes: postnatal growth retardation, decreased body weight, abnormal pituitary secretion, decreased circulating insulin-like growth factor I level, maternal imprinting, decreased growth hormone level Allele Detail: Targeted

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Cite this (MGI Cat# 3656483, RRID:MGI:3656483)

Source Database: MGI, catalog # 3656483
Genetic Background: involves: CAST/EiJ * C57BL/6J-Socs2
Affected Genes: Mohg4
Genomic Alteration: CAST/EiJ
Availability: Availability unknown check source stock center
Reference: PMID:16670015
Notes: decreased body weight, postnatal growth retardation, decreased total fat pad weight Allele Detail: QTL

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Cite this (MGI Cat# 5308233, RRID:MGI:5308233)

Source Database: MGI, catalog # 5308233
Genetic Background: involves: BALB/cAnN * C3H/HeH * C57BL/6J * FVB/N
Affected Genes: Gars
Genomic Alteration: C201R; Tg(CAG-GARS)DRwb; Nmf249
Availability: Availability unknown check source stock center
Reference: PMID:22144914
Notes: abnormal axon morphology, abnormal neuromuscular synapse morphology, decreased body weight, mortality/aging Allele Detail: Chemically induced (ENU), Transgenic, Spontaneous

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Cite this (MGI Cat# 5613396, RRID:MGI:5613396)

Source Database: MGI, catalog # 5613396
Genetic Background: involves: C57BL/6J
Affected Genes: Arntl
Genomic Alteration: tm1.2Shbi
Availability: Availability unknown check source stock center
Reference: PMID:21966465
Notes: abnormal locomotor circadian rhythm, abnormal lipid level, behavior/neurological phenotype, decreased body weight, decreased circulating HDL cholesterol level, decreased circulating VLDL triglyceride level, decreased susceptibility to diet-induced obesity, decreased total body fat amount, decreased white fat cell size, hepatic steatosis, increased circulating HDL cholesterol level, increased circulating LDL cholesterol level, increased circulating VLDL cholesterol level, increased circulating cholesterol level, increased circulating free fatty acid level, increased circulating triglyceride level, increased liver triglyceride level, increased respiratory quotient, increased triglyceride level, abnormal gluconeogenesis, abnormal glucose homeostasis, decreased circulating insulin level, decreased insulin secretion, enlarged pancreatic islets, homeostasis/metabolism phenotype, hyperglycemia, impaired glucose tolerance, increased sebum secretion Allele Detail: Targeted

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Cite this (MGI Cat# 5009030, RRID:MGI:5009030)

Source Database: MGI, catalog # 5009030
Genetic Background: involves: 101/H * C3H/HeH * C3H/HeSnJ * C57BL/6J
Affected Genes: Gy
Genomic Alteration: Gy
Availability: Availability unknown check source stock center
Reference: PMID:8266820
Notes: abnormal calcium ion homeostasis, decreased intestinal calcium absorption, decreased body weight, decreased circulating phosphate level Allele Detail: Radiation induced

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Cite this (MGI Cat# 5781700, RRID:MGI:5781700)

Source Database: MGI, catalog # 5781700
Genetic Background: B6JTyr;B6N-Plekhm2/Wtsi
Affected Genes: Plekhm2
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: decreased body weight, decreased body weight, increased leukocyte cell number, decreased hematocrit, decreased hemoglobin content Allele Detail: Targeted

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Cite this (MGI Cat# 2677931, RRID:MGI:2677931)

Source Database: MGI, catalog # 2677931
Genetic Background: Not Specified
Affected Genes:
Genomic Alteration: gro25
Availability: Availability unknown check source stock center
Reference: PMID:12955145
Notes: decreased body size, azoospermia, decreased body weight Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3038202, RRID:MGI:3038202)

Source Database: MGI, catalog # 3038202
Genetic Background: involves: C57BL/6J * M. m. castaneus
Affected Genes: Pbwg2
Genomic Alteration: M. m. castaneus
Availability: Availability unknown check source stock center
Reference: PMID:15056934, PMID:16174331
Notes: postnatal growth retardation, decreased body weight Allele Detail: QTL

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Cite this (MGI Cat# 3653638, RRID:MGI:3653638)

Source Database: MGI, catalog # 3653638
Genetic Background: involves: C3H/HeJ * C57BL/6J
Affected Genes: Kl
Genomic Alteration: kl
Availability: Availability unknown check source stock center
Reference: PMID:12475907, PMID:11016890, PMID:12446599
Notes: abnormal contextual conditioning behavior, abnormal cued conditioning behavior, abnormal long term object recognition memory, abnormal nervous system physiology, oxidative stress, postnatal growth retardation, premature death, decreased osteoclast cell number, decreased B cell number, decreased body weight, osteopetrosis, short femur, hypoglycemia, decreased insulin secretion, increased insulin sensitivity, decreased circulating insulin level Allele Detail: Transgenic

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Cite this (MGI Cat# 5754859, RRID:MGI:5754859)

Source Database: MGI, catalog # 5754859
Genetic Background: B6J.129P2-Del(16Hspa13-App)3Yah
Affected Genes: Del(16Hspa13-App)3Yah
Genomic Alteration: Del(16Hspa13-App)3Yah
Availability: Availability unknown check source stock center
Reference: PMID:25803843
Notes: abnormal cellular respiration, abnormal mitochondrial chromosome morphology, abnormal mitochondrial physiology, abnormal muscle physiology, abnormal skeletal muscle fiber type ratio, abnormal skeletal muscle morphology, decreased body weight, decreased grip strength, decreased skeletal muscle mass, enhanced coordination, hyperactivity Allele Detail: Targeted

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Cite this (MGI Cat# 3804962, RRID:MGI:3804962)

Source Database: MGI, catalog # 3804962
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Lin7c
Genomic Alteration: tm1Dsb
Availability: Availability unknown check source stock center
Reference: PMID:17923534
Notes: increased kidney apoptosis, abnormal renal tubule epithelium morphology, single kidney, decreased body weight, decreased creatinine clearance, decreased kidney weight, decreased urine osmolality, dilated renal tubules, increased blood urea nitrogen level, increased urine sodium level, polycystic kidney, polyuria, renal interstitial fibrosis, abnormal kidney physiology, abnormal kidney morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3032571, RRID:MGI:3032571)

Source Database: MGI, catalog # 3032571
Genetic Background: involves: AKR/J * C57BL/6By
Affected Genes: Tg
Genomic Alteration: cog
Availability: Availability unknown check source stock center
Reference: PMID:3803305, PMID:1508304
Notes: anemia, decreased body weight, decreased body weight, decreased circulating thyroxine level, decreased circulating triiodothyronine level, decreased hematocrit, enlarged thyroid gland, increased circulating thyroid-stimulating hormone level, abnormal myelination, decreased brain weight Allele Detail: Spontaneous

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Cite this (MGI Cat# 3846426, RRID:MGI:3846426)

Source Database: MGI, catalog # 3846426
Genetic Background: B6.129S7-Cisd2
Affected Genes: Cisd2
Genomic Alteration: tm1Tfts
Availability: Availability unknown check source stock center
Reference: PMID:19451219
Notes: abnormal myocardium layer morphology, small thoracic cavity, abnormal coat/hair pigmentation, abnormal defecation, prominent ears, exophthalmos, abnormal glucose homeostasis, abnormal mitochondrion morphology, abnormal muscle fiber morphology, abnormal respiratory function, axon degeneration, blindness, corneal opacity, decreased total body fat amount, decreased body mass index, decreased body size, decreased body weight, decreased bone mineral density, decreased trabecular bone thickness, decreased fluid intake, decreased food intake, decreased hair follicle number, decreased insulin secretion, abnormal respiratory electron transport chain, decreased oxygen consumption, decreased subcutaneous adipose tissue amount, decreased tidal volume, oliguria, demyelination, impaired glucose tolerance, increased insulin sensitivity, kyphosis, lordosis, muscle degeneration, neurodegeneration, postnatal growth retardation, premature aging, premature death, retinal neovascularization, thick epidermis, abnormal optic nerve morphology Allele Detail: Targeted

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Cite this (MGI Cat# 4830571, RRID:MGI:4830571)

Source Database: MGI, catalog # 4830571
Genetic Background: involves: 129X1/SvJ * C57BL/6
Affected Genes: Mark2, Mark3
Genomic Alteration: tm1Hpw
Availability: Availability unknown check source stock center
Reference: PMID:20733003
Notes: decreased body weight, postnatal lethality Allele Detail: Targeted

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Cite this (MGI Cat# 3789956, RRID:MGI:3789956)

Source Database: MGI, catalog # 3789956
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Affected Genes: Cry1, Cry2
Genomic Alteration: tm1Hnos; tm1Asn
Availability: Availability unknown check source stock center
Reference: PMID:15860530
Notes: abnormal baroreceptor physiology, abnormal circadian behavior, abnormal vasoconstriction, decreased body weight, abnormal circadian regulation of heart rate, abnormal circadian regulation of systemic arterial blood pressure Allele Detail: Targeted

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Cite this (MGI Cat# 5749268, RRID:MGI:5749268)

Source Database: MGI, catalog # 5749268
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6
Affected Genes: Zfyve26
Genomic Alteration: tm1.1Cahb
Availability: Availability unknown check source stock center
Reference: PMID:24367272
Notes: Purkinje cell degeneration, abnormal gait, abnormal posture, abnormal urinary bladder physiology, astrocytosis, ataxia, axon degeneration, behavior/neurological phenotype, brain atrophy, decreased body weight, decreased brain weight, enlarged urinary bladder, impaired coordination, kyphosis, motor neuron degeneration, abnormal lysosome physiology, delayed axon extension, abnormal lysosome morphology Allele Detail: Targeted

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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

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Cite this (MGI Cat# 5440503, RRID:MGI:5440503)

Source Database: MGI, catalog # 5440503
Genetic Background: C57BL/6-Tenm4
Affected Genes: Tenm4
Genomic Alteration: Tg(Col2a1-Hspg2)2Yoya
Availability: Availability unknown check source stock center
Reference: PMID:22915103
Notes: abnormal oligodendrocyte apoptosis, abnormal oligodendrocyte morphology, abnormal spinal cord dorsal column morphology, abnormal spinal cord white matter morphology, decreased body size, decreased body weight, demyelination, hindlimb paralysis, tremors Allele Detail: Transgenic

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