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on page 1 showing 20 out of 2,034 results from 1 sources

Cite this (MGI Cat# 2673175, RRID:MGI:2673175)

Source Database: MGI, catalog # 2673175
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
Affected Genes: Hoxb4
Genomic Alteration: tm1Nrm
Availability: Availability unknown check source stock center
Reference: PMID:9012503, PMID:11518511
Notes: abnormal sternum morphology, abnormal ventral body wall morphology, abnormal ventral body wall morphology, neonatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance, abnormal cervical vertebrae morphology, split sternum, abnormal sternum morphology, decreased body size, pallor, abnormal abdominal wall morphology, respiratory distress, abnormal heart position or orientation, absent pericardium, edema, abnormal body wall morphology, dilated heart ventricle, thin ventricular wall, thin interventricular septum, diaphragmatic hernia, abnormal heart morphology Allele Detail: Targeted

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Cite this (MGI Cat# 2664326, RRID:MGI:2664326)

Source Database: MGI, catalog # 2664326
Genetic Background: FVB.129-Col11a2
Affected Genes: Col11a2
Genomic Alteration: tm1Mne
Availability: Availability unknown check source stock center
Reference: PMID:11668593, PMID:10581026
Notes: postnatal growth retardation, abnormal tectorial membrane morphology, enlarged tectorial membrane, sensorineural hearing loss, nonsyndromic hearing loss, abnormal cranium morphology, increased or absent threshold for auditory brainstem response, increased or absent threshold for auditory brainstem response, abnormal nasal bone morphology, abnormal articular cartilage morphology, disorganized long bone epiphyseal plate, prominent forehead, abnormal chondrocyte morphology, impaired hearing, impaired hearing, decreased body size, short snout, triangular face 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# 2664240, RRID:MGI:2664240)

Source Database: MGI, catalog # 2664240
Genetic Background: Not Specified
Affected Genes: Mybl1
Genomic Alteration: tm1Epr
Availability: Availability unknown check source stock center
Reference: PMID:9109487, PMID:21750041
Notes: arrest of male meiosis, arrest of male meiosis, abnormal Sertoli cell morphology, azoospermia, azoospermia, postnatal growth retardation, male infertility, male infertility, decreased body size, small seminiferous tubules, small testis, arrest of spermatogenesis, decreased testis weight, hunched posture, wrinkled skin, abnormal mammary gland epithelium morphology, abnormal mammary gland growth during lactation, abnormal mammary gland growth during pregnancy, abnormal nursing, abnormal spermatocyte morphology, decreased male germ cell number, abnormal male germ cell apoptosis, abnormal synaptonemal complex Allele Detail: Targeted

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Cite this (MGI Cat# 5817790, RRID:MGI:5817790)

Source Database: MGI, catalog # 5817790
Genetic Background: C3HeB/FeJ-Scube3
Affected Genes: Scube3
Genomic Alteration: m1Mhda
Availability: Availability unknown check source stock center
Reference: PMID:27815347
Notes: abnormal anxiety-related response, abnormal body composition, abnormal bone ossification, abnormal digit morphology, abnormal enzyme/coenzyme activity, abnormal food intake, abnormal heart left ventricle morphology, small incus, abnormal inner ear morphology, abnormal interventricular septum morphology, abnormal lumbar vertebrae morphology, abnormal malleus head morphology, abnormal malleus morphology, abnormal metacarpal bone morphology, abnormal metatarsal bone morphology, abnormal middle ear morphology, abnormal middle ear ossicle morphology, abnormal posture, abnormal tarsal bone morphology, abnormal temporal bone morphology, abnormal thoracic vertebrae morphology, abnormal vertebral pedicle morphology, decreased body fat mass, decreased body size, decreased bone mineral content, decreased bone mineral density, decreased circulating cholesterol level, decreased circulating free fatty acid level, decreased circulating glucose level, decreased circulating glycerol level, decreased circulating phosphate level, decreased circulating serum albumin level, decreased circulating total protein level, decreased circulating triglyceride level, decreased grip strength, decreased lean body mass, decreased pulmonary respiratory rate, decreased vertical activity, hypoactivity, improved glucose tolerance, increased alkaline phosphatase activity, increased blood urea nitrogen level, increased bone resorption, increased circulating calcium level, increased circulating creatinine level, increased circulating potassium level, increased fluid intake, increased or absent threshold for auditory brainstem response, kinked tail, polyuria, prolonged QRS complex duration, rib fusion, short femur, short tail, thin ventricular wall, increased blood uric acid level, abnormal renal filtration, fused phalanges, abnormal pectoral girdle bone morphology, conductive hearing loss, decreased urine uric acid level, decreased urine albumin level, decreased urine creatinine level, decreased urine glucose level, decreased urine protein level, small middle ear ossicles Allele Detail: Chemically induced (ENU)

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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# 5790646, RRID:MGI:5790646)

Source Database: MGI, catalog # 5790646
Genetic Background: involves: BALB/cAnNHsd * C3H/HeNHsd
Affected Genes: Gnptab
Genomic Alteration: nym
Availability: Availability unknown check source stock center
Reference: PMID:25107912
Notes: abnormal facial morphology, abnormal skeleton morphology, abnormal spine curvature, decreased body size, decreased survivor rate, flattened snout, kyphosis, postnatal growth retardation, premature death, thick eyelids, abnormal cerebellar cortex morphology, abnormal cerebellar molecular layer, abnormal chondrocyte morphology, abnormal enzyme/coenzyme activity, abnormal hippocampus CA1 region morphology, abnormal hippocampus CA3 region morphology, abnormal pancreas morphology, abnormal pancreatic acinar cell morphology, brain inflammation, lysosomal protein accumulation, thick skin, abnormal fertility/fecundity, abnormal gait, impaired coordination, limb grasping, penis prolapse, prenatal lethality, incomplete penetrance, Purkinje cell degeneration, abnormal cognition, ataxia, brain atrophy, cerebellum atrophy, decreased brain size, progressive muscle weakness, Purkinje cell axonal dystrophy, abnormal cerebellum white matter morphology, astrocytosis, axonal spheroids, demyelination, abnormal skin turgor, small nasal bridge Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3808825, RRID:MGI:3808825)

Source Database: MGI, catalog # 3808825
Genetic Background: involves: C57BL/6JJcl * DBA/2JJcl
Affected Genes:
Genomic Alteration: Rgsc597
Availability: Availability unknown check source stock center
Reference:
Notes: decreased body size Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3774506, RRID:MGI:3774506)

Source Database: MGI, catalog # 3774506
Genetic Background: involves: 129S7/SvEvBrd
Affected Genes: Kcna2
Genomic Alteration: tm1Tem
Availability: Availability unknown check source stock center
Reference: PMID:17925011
Notes: abnormal brain wave pattern, abnormal sleep pattern, decreased body size, postnatal lethality, complete penetrance, seizures Allele Detail: Targeted

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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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Cite this (MGI Cat# 5000309, RRID:MGI:5000309)

Source Database: MGI, catalog # 5000309
Genetic Background: involves: 129S/Sv * C57BL/6 * FVB/N * SJL
Affected Genes: Sos1
Genomic Alteration: tm1.2Rak
Availability: Availability unknown check source stock center
Reference: PMID:21041952
Notes: abnormal cardiovascular system physiology, abnormal craniofacial morphology, abnormal fetal cardiomyocyte proliferation, abnormal frontal bone morphology, abnormal heart morphology, aortic valve stenosis, cardiac fibrosis, decreased body length, decreased body size, decreased body weight, decreased cranium height, heart right ventricle hypertrophy, hemorrhage, myocardial fiber degeneration, ocular hypertelorism, ostium secundum atrial septal defect, embryonic lethality during organogenesis, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance, pericardial effusion, premature death, skin edema, thick aortic valve cusps, thick interventricular septum, ventricular septal defect Allele Detail: Targeted

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Cite this (MGI Cat# 3692745, RRID:MGI:3692745)

Source Database: MGI, catalog # 3692745
Genetic Background: involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N
Affected Genes: Gfap
Genomic Alteration: tm2Mes
Availability: Availability unknown check source stock center
Reference: PMID:17065456
Notes: abnormal astrocyte morphology, abnormal brain iron level, gliosis, decreased body size, increased susceptibility to pharmacologically induced seizures Allele Detail: Targeted

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Cite this (MGI Cat# 4420930, RRID:MGI:4420930)

Source Database: MGI, catalog # 4420930
Genetic Background: 129S-Wwtr1/J
Affected Genes: Wwtr1
Genomic Alteration: tm1Benj
Availability: Availability unknown check source stock center
Reference:
Notes: prenatal lethality, incomplete penetrance, premature death, reduced female fertility, decreased body size, hypoactivity, polycystic kidney, emphysema, overexpanded pulmonary alveoli, enlarged kidney, intestinal inflammation, lung inflammation, decreased fat cell size, abnormal pulmonary alveolus wall morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5509043, RRID:MGI:5509043)

Source Database: MGI, catalog # 5509043
Genetic Background: involves: C57BL/6J * C57BL/6N
Affected Genes: Cluap1
Genomic Alteration: tm1a(KOMP)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:23351563
Notes: embryonic lethality during organogenesis, complete penetrance, abnormal embryo turning, decreased body size, enlarged pericardium, kinked neural tube, absent embryonic cilia Allele Detail: Targeted

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Cite this (MGI Cat# 4443126, RRID:MGI:4443126)

Source Database: MGI, catalog # 4443126
Genetic Background: involves: 129S/SvEv * C57BL/6
Affected Genes: Pex7
Genomic Alteration: tm1Nbra
Availability: Availability unknown check source stock center
Reference: PMID:20060764
Notes: decreased body weight, slow postnatal weight gain, decreased body size, decreased birth weight, decreased birth body size, cataract, decreased litter size, reduced fertility, increased sensitivity to induced morbidity/mortality, increased susceptibility to weight loss, decreased fatty acid level, abnormal enzyme/coenzyme activity, abnormal cell physiology, abnormal lens fiber morphology, abnormal lens morphology, abnormal lens capsule morphology, delayed bone ossification, increased fatty acid level, decreased saturated fatty acid level, lipidosis, hepatic steatosis, abnormal heart morphology, abnormal adrenal gland morphology, enlarged liver, liver degeneration, liver inflammation, demyelination, abnormal spinal cord morphology, abnormal hippocampus morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3697171, RRID:MGI:3697171)

Source Database: MGI, catalog # 3697171
Genetic Background: involves: C57BL/6JEiJ * P/J
Affected Genes: Ass1
Genomic Alteration: fold
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal hair follicle morphology, abnormal hair follicle development, delayed hair appearance, hearing/vestibular/ear phenotype, postnatal lethality, premature death, decreased body size, sparse hair, vision/eye phenotype, wrinkled skin Allele Detail: Spontaneous

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Cite this (MGI Cat# 5795741, RRID:MGI:5795741)

Source Database: MGI, catalog # 5795741
Genetic Background: CByJ.Cg-smsz/GrsrJ
Affected Genes:
Genomic Alteration: smsz
Availability: Availability unknown check source stock center
Reference:
Notes: decreased body size, prenatal lethality, incomplete penetrance, cataract Allele Detail: Spontaneous

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Cite this (MGI Cat# 2176726, RRID:MGI:2176726)

Source Database: MGI, catalog # 2176726
Genetic Background: involves: 129S2/SvPas * C57BL/6
Affected Genes: Bcl2
Genomic Alteration: tm1Mpin
Availability: Availability unknown check source stock center
Reference: PMID:8755480, PMID:10321489
Notes: abnormal L3 dorsal root ganglion morphology, abnormal facial motor nucleus morphology, abnormal superior cervical ganglion morphology, abnormal sympathetic neuron morphology, increased blood urea nitrogen level, premature death, decreased body size, decreased sensory neuron number, abnormal optic nerve morphology, polycystic kidney, motor neuron degeneration, retinal ganglion cell degeneration, increased circulating creatinine level Allele Detail: Targeted

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Cite this (MGI Cat# 5608670, RRID:MGI:5608670)

Source Database: MGI, catalog # 5608670
Genetic Background: involves: C57BL/6J
Affected Genes: Myo5a
Genomic Alteration: d-l35J
Availability: Availability unknown check source stock center
Reference:
Notes: ataxia, lethality at weaning, complete penetrance, diluted coat color, impaired righting response, decreased body size, impaired balance Allele Detail: Spontaneous

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Cite this (MGI Cat# 2176507, RRID:MGI:2176507)

Source Database: MGI, catalog # 2176507
Genetic Background: involves: 129S4/SvJae
Affected Genes: H2-DMa
Genomic Alteration: tm1Luc
Availability: Availability unknown check source stock center
Reference: PMID:10843678, PMID:8598041, PMID:9551884
Notes: abnormal positive T cell selection, premature death, decreased interferon-gamma secretion, increased susceptibility to bacterial infection, decreased CD4-positive, alpha beta T cell number, decreased CD4-positive, alpha beta T cell number, abnormal level of surface class II molecules, decreased body size, abnormal CD4-positive, alpha-beta T cell physiology, abnormal antigen presentation via MHC class II Allele Detail: Targeted

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