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on page 1 showing 20 out of 1,123 results from 1 sources

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# 2448446, RRID:MGI:2448446)

Source Database: MGI, catalog # 2448446
Genetic Background: involves: DBA/1J
Affected Genes: Spta1
Genomic Alteration: sph-ha
Availability: Availability unknown check source stock center
Reference: PMID:6234993
Notes: cardiac hypertrophy, enlarged spleen, enlarged spleen, erythroblastosis, jaundice, jaundice, jaundice, microcytic anemia, microcytosis, abnormal reticulocyte morphology, abnormal erythrocyte morphology, enlarged liver, hemolytic anemia, abnormal bone marrow morphology, decreased hematocrit, decreased mean corpuscular volume, decreased hemoglobin content, postnatal lethality, incomplete penetrance, prenatal lethality, incomplete penetrance, hypochromic microcytic anemia, infertility, abnormal skin pigmentation, postnatal lethality, incomplete penetrance Allele Detail: Spontaneous

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Cite this (MGI Cat# 3037157, RRID:MGI:3037157)

Source Database: MGI, catalog # 3037157
Genetic Background: Not Specified
Affected Genes: Csrp3
Genomic Alteration: tm1Crni
Availability: Availability unknown check source stock center
Reference: PMID:9039266, PMID:14966518, PMID:18713466
Notes: decreased cardiac muscle contractility, dilated cardiomyopathy, dilated cardiomyopathy, dilated heart left ventricle, dilated heart left ventricle, postnatal lethality, incomplete penetrance, cardiac hypertrophy, enlarged heart, decreased ventricle muscle contractility, cardiac interstitial fibrosis, increased heart weight, abnormal cell cytoskeleton morphology, abnormal intercalated disc morphology, enlarged myocardial fiber Allele Detail: Targeted

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Cite this (MGI Cat# 3626194, RRID:MGI:3626194)

Source Database: MGI, catalog # 3626194
Genetic Background: involves: 129S6/SvEvTac * C57BL/6
Affected Genes: Ep300
Genomic Alteration: tm3Pkb
Availability: Availability unknown check source stock center
Reference: PMID:16237459
Notes: postnatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5766740, RRID:MGI:5766740)

Source Database: MGI, catalog # 5766740
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/cJ
Affected Genes: Cftr
Genomic Alteration: tm1Hsc
Availability: Availability unknown check source stock center
Reference: PMID:8589719, PMID:11102538
Notes: abnormal intestine physiology, postnatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 2680150, RRID:MGI:2680150)

Source Database: MGI, catalog # 2680150
Genetic Background: involves: 129S6/SvEvTac * C57BL/6
Affected Genes: Mef2a
Genomic Alteration: tm1Eno
Availability: Availability unknown check source stock center
Reference: PMID:12379849
Notes: respiratory system phenotype, decreased heart rate, dilated heart right ventricle, premature death, postnatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5561080, RRID:MGI:5561080)

Source Database: MGI, catalog # 5561080
Genetic Background: involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J
Affected Genes: Aplp2, Lrp4
Genomic Alteration: tm1Her; tm1Dbo
Availability: Availability unknown check source stock center
Reference: PMID:23986861
Notes: abnormal neuromuscular synapse morphology, postnatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 3767229, RRID:MGI:3767229)

Source Database: MGI, catalog # 3767229
Genetic Background: Not Specified
Affected Genes: hl
Genomic Alteration: hl
Availability: Availability unknown check source stock center
Reference: PMID:13675267, PMID:13715315
Notes: abnormal hair growth, postnatal lethality, incomplete penetrance, postnatal lethality, incomplete penetrance, premature death, premature hair loss, abnormal bone strength, abnormal skeleton physiology, fragile skeleton, maternal effect, abnormal hair follicle morphology, abnormal hair follicle development, hair follicle degeneration Allele Detail: Spontaneous

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Cite this (MGI Cat# 4999807, RRID:MGI:4999807)

Source Database: MGI, catalog # 4999807
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/c * ICR
Affected Genes: Nek7
Genomic Alteration: tm1Mot
Availability: Availability unknown check source stock center
Reference: PMID:20473324
Notes: embryonic lethality during organogenesis, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance, perinatal lethality, incomplete penetrance, postnatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, decreased birth weight, postnatal growth retardation, binucleate, polyploidy, aneuploidy, chromosomal instability, abnormal mitosis Allele Detail: Targeted

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Cite this (MGI Cat# 3522090, RRID:MGI:3522090)

Source Database: MGI, catalog # 3522090
Genetic Background: either: (129X1/SvJ) or (involves: 129/Sv * C57BL/6J)
Affected Genes: Nppc
Genomic Alteration: tm1Yog
Availability: Availability unknown check source stock center
Reference: PMID:11259675
Notes: decreased long bone epiphyseal plate size, abnormal vertebral epiphyseal plate morphology, decreased width of hypertrophic chondrocyte zone, abnormal long bone epiphyseal plate proliferative zone, abnormal cartilage morphology, decreased body length, decreased body weight, disproportionate dwarf, postnatal growth retardation, decreased cranium height, postnatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 4819863, RRID:MGI:4819863)

Source Database: MGI, catalog # 4819863
Genetic Background: B6.C3-Spta1/BrkJ
Affected Genes: Spta1
Genomic Alteration: sph
Availability: Availability unknown check source stock center
Reference:
Notes: neonatal lethality, incomplete penetrance, postnatal lethality, incomplete penetrance Allele Detail: Spontaneous

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Cite this (MGI Cat# 2447790, RRID:MGI:2447790)

Source Database: MGI, catalog # 2447790
Genetic Background: involves: 129 * C57BL/6J
Affected Genes: Adcyap1r1
Genomic Alteration: tm1Bbt
Availability: Availability unknown check source stock center
Reference: PMID:11193864, PMID:10792006, PMID:11792830, PMID:11425915
Notes: prolonged diestrus, postnatal lethality, incomplete penetrance, decreased body weight, increased circulating insulin level, decreased circulating insulin level, impaired glucose tolerance, increased susceptibility to bacterial infection, shortened circadian behavior period, delayed circadian behavior phase, reduced female fertility, prolonged estrous cycle Allele Detail: Targeted

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Cite this (MGI Cat# 2655569, RRID:MGI:2655569)

Source Database: MGI, catalog # 2655569
Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6J
Affected Genes: Traf2
Genomic Alteration: tm1Mak
Availability: Availability unknown check source stock center
Reference: PMID:9390694
Notes: postnatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5442772, RRID:MGI:5442772)

Source Database: MGI, catalog # 5442772
Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or B6.129P2-Tph2
Affected Genes: Tph2
Genomic Alteration: tm1Pasq
Availability: Availability unknown check source stock center
Reference: PMID:23007167
Notes: postnatal lethality, incomplete penetrance, postnatal growth retardation, behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 2175201, RRID:MGI:2175201)

Source Database: MGI, catalog # 2175201
Genetic Background: Not Specified
Affected Genes: Pax6
Genomic Alteration: Sey-2H
Availability: Availability unknown check source stock center
Reference:
Notes: embryonic lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, postnatal lethality, incomplete penetrance, decreased birth body size, white spotting, exencephaly Allele Detail: Chemically and radiation induced

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Cite this (MGI Cat# 5085292, RRID:MGI:5085292)

Source Database: MGI, catalog # 5085292
Genetic Background: B6.129P2-Llgl2
Affected Genes: Llgl2
Genomic Alteration: Gt(XS0846)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:21606200
Notes: abnormal placenta labyrinth morphology, abnormal placental labyrinth vasculature morphology, decreased birth body size, decreased fetal weight, decreased placenta weight, integument phenotype, postnatal lethality, incomplete penetrance, small placenta, abnormal placenta fetal blood space morphology, increased placenta intervillous maternal lacunae size, abnormal placenta intervillous maternal lacunae morphology, abnormal placental labyrinth villi branching morphogenesis, decreased placental labyrinth size, abnormal placental labyrinth villi morphology Allele Detail: Gene trapped

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Cite this (MGI Cat# 4818399, RRID:MGI:4818399)

Source Database: MGI, catalog # 4818399
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Affected Genes: Kcmf1
Genomic Alteration: Gt(XE080)Byg
Availability: Availability unknown check source stock center
Reference: PMID:20473331
Notes: decreased survivor rate, perinatal lethality, incomplete penetrance, postnatal lethality, incomplete penetrance Allele Detail: Gene trapped

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Cite this (MGI Cat# 3710405, RRID:MGI:3710405)

Source Database: MGI, catalog # 3710405
Genetic Background: BALB/cByJ-Lpin1
Affected Genes: Lpin1
Genomic Alteration: fld
Availability: Availability unknown check source stock center
Reference: PMID:11138012, PMID:2050689, PMID:2722772, PMID:10884287, PMID:18669885
Notes: abnormal Schwann cell morphology, abnormal cholesterol homeostasis, abnormal enzyme/coenzyme activity, abnormal gait, abnormal hair growth, abnormal lipid homeostasis, abnormal myelin sheath morphology, abnormal phospholipid level, abnormal sciatic nerve morphology, axon degeneration, decreased triglyceride level, delayed female fertility, disheveled coat, distended abdomen, enlarged liver, enlarged liver, female infertility, increased cholesterol level, increased fatty acid level, limb grasping, male infertility, pale liver, postnatal lethality, incomplete penetrance, premature death, ruffled hair, tremors, increased triglyceride level, abnormal lipid level, abnormal PNS glial cell morphology, abnormal axon morphology, abnormal fat cell morphology, abnormal brown adipose tissue physiology, abnormal aorta morphology, abnormal brown adipose tissue morphology, decreased hormone-sensitive lipase activity, decreased inguinal fat pad weight, abnormal white adipose tissue physiology, decreased body weight, decreased brown adipose tissue mass, decreased brown adipose tissue mass, decreased circulating LDL cholesterol level, decreased circulating VLDL cholesterol level, decreased fatty acid level, decreased insulin secretion, decreased lean body mass, decreased white adipose tissue mass, impaired glucose tolerance, increased circulating HDL cholesterol level, increased circulating insulin level, insulin resistance, abnormal triglyceride level, abnormal epididymal fat pad morphology, decreased interscapular fat pad weight, decreased epididymal fat pad weight, lethality at weaning, incomplete penetrance, decreased survivor rate, retarded hair growth, abnormal motor coordination/ balance, impaired limb coordination, increased circulating VLDL triglyceride level, abnormal fat cell morphology, decreased brown fat cell lipid droplet size, decreased white fat cell lipid droplet size, decreased circulating leptin level, decreased white adipose tissue mass, increased circulating triglyceride level, increased liver triglyceride level, increased liver triglyceride level, decreased lipoprotein lipase activity, decreased triglyceride lipase activity Allele Detail: Spontaneous

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Cite this (MGI Cat# 2177662, RRID:MGI:2177662)

Source Database: MGI, catalog # 2177662
Genetic Background: involves: 129 * C57BL/6J
Affected Genes: Hmx3
Genomic Alteration: tm1Tlu
Availability: Availability unknown check source stock center
Reference: PMID:9435283
Notes: abnormal crista ampullaris morphology, abnormal decidualization, abnormal lateral semicircular canal morphology, abnormal otolith organ morphology, abnormal vestibular saccule morphology, abnormal utricle morphology, abnormal vestibular labyrinth morphology, circling, failure of embryo implantation, hyperactivity, postnatal lethality, incomplete penetrance, reduced female fertility, vestibular saccular macula degeneration, utricular macular degeneration Allele Detail: Targeted

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Cite this (MGI Cat# 2174947, RRID:MGI:2174947)

Source Database: MGI, catalog # 2174947
Genetic Background: involves: 129S7/SvEvBrd
Affected Genes: Edn3
Genomic Alteration: tm1Ywa
Availability: Availability unknown check source stock center
Reference: PMID:8001160
Notes: abnormal colon morphology, absent enteric neurons, aganglionic megacolon, postnatal lethality, incomplete penetrance, premature death, variable body spotting Allele Detail: Targeted

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