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on page 1 showing 20 out of 1,126 results from 1 sources

Cite this (MGI Cat# 4360658, RRID:MGI:4360658)

Source Database: MGI, catalog # 4360658
Genetic Background: involves: C57BL/6 * CBA
Affected Genes: Grin2b
Genomic Alteration: tm1Mim
Availability: Availability unknown check source stock center
Reference: PMID:22153375, PMID:8789948
Notes: abnormal AMPA-mediated synaptic currents, absent long term depression, absent gastric milk in neonates, disorganized barrel cortex, neonatal lethality, complete penetrance, absence of NMDA-mediated synaptic currents, no suckling reflex Allele Detail: Targeted

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Cite this (MGI Cat# 5825470, RRID:MGI:5825470)

Source Database: MGI, catalog # 5825470
Genetic Background: involves: 129S6/SvEvTac * BALB/c
Affected Genes: Cnn3
Genomic Alteration: tm1.2Hjum
Availability: Availability unknown check source stock center
Reference: PMID:26046660
Notes: neonatal lethality, complete penetrance, abnormal nervous system development, exencephaly Allele Detail: Targeted

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Cite this (MGI Cat# 3042284, RRID:MGI:3042284)

Source Database: MGI, catalog # 3042284
Genetic Background: involves: 129S7/SvEvBrd
Affected Genes: Fst
Genomic Alteration: tm1Zuk
Availability: Availability unknown check source stock center
Reference: PMID:7885475
Notes: decreased fetal size, abnormal rib development, respiratory failure, pallor, decreased lumbar vertebrae number, thick epidermis, tight skin, abnormal vibrissa morphology, shiny skin, fetal growth retardation, cyanosis, decreased rib number, decreased fetal weight, absent hard palate, decreased skeletal muscle mass, hyperkeratosis, neonatal lethality, complete penetrance, growth retardation of incisors Allele Detail: Targeted

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Cite this (MGI Cat# 3044921, RRID:MGI:3044921)

Source Database: MGI, catalog # 3044921
Genetic Background: involves: 129S1/SvImJ * NMRI
Affected Genes: Tbx18
Genomic Alteration: tm1.1Akis
Availability: Availability unknown check source stock center
Reference: PMID:15155583
Notes: small intervertebral disk, rib fusion, fusion of atlas and occipital bones, abnormal lumbar vertebrae morphology, neonatal lethality, complete penetrance, abnormal vertebrae morphology, abnormal vertebrae development, decreased birth body size, abnormal spinal nerve morphology, fused dorsal root ganglion, abnormal dorsal-ventral polarity of the somites, abnormal thoracic vertebrae morphology, abnormal rib morphology, abnormal vertebral arch morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5311903, RRID:MGI:5311903)

Source Database: MGI, catalog # 5311903
Genetic Background: Not Specified
Affected Genes: Trp63
Genomic Alteration: tm1Sin
Availability: Availability unknown check source stock center
Reference: PMID:22274697
Notes: decreased fetal size, abnormal keratinocyte physiology, abnormal skin development, absent hair follicles, absent sebaceous gland, absent epidermis, abnormal embryo development, abnormal keratinocyte morphology, decreased keratinocyte proliferation, abnormal limb development, abnormal craniofacial development, neonatal lethality, complete penetrance, abnormal keratinocyte differentiation, dehydration Allele Detail: Targeted

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Cite this (MGI Cat# 3527491, RRID:MGI:3527491)

Source Database: MGI, catalog # 3527491
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
Affected Genes: Neurog1
Genomic Alteration: tm1And
Availability: Availability unknown check source stock center
Reference: PMID:9539122
Notes: abnormal cranial nerve morphology, abnormal superior vagus ganglion morphology, neonatal lethality, complete penetrance, abnormal suckling behavior, abnormal accessory nerve morphology, abnormal trigeminal nerve morphology, absent trigeminal ganglion, abnormal superior glossopharyngeal ganglion morphology, abnormal cranial ganglia morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3715253, RRID:MGI:3715253)

Source Database: MGI, catalog # 3715253
Genetic Background: involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6
Affected Genes: Hand2
Genomic Alteration: tm1Dsr; tm1Cse
Availability: Availability unknown check source stock center
Reference: PMID:19341725, PMID:17531968
Notes: palatal shelves fail to meet at midline, neonatal lethality, complete penetrance, cleft secondary palate, tongue hypoplasia, palatal shelf hypoplasia, cleft primary palate, abnormal suckling behavior, abnormal palatal shelf elevation Allele Detail: Targeted

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Cite this (MGI Cat# 3629689, RRID:MGI:3629689)

Source Database: MGI, catalog # 3629689
Genetic Background: either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J) or (involves: 129S/SvEv * MF1)
Affected Genes: Igf1, Igf2
Genomic Alteration: tm1Rob; tm1Arge
Availability: Availability unknown check source stock center
Reference: PMID:8402901
Notes: thin epidermis stratum spinosum, neonatal lethality, complete penetrance, decreased birth weight, maternal imprinting, delayed bone ossification, respiratory failure Allele Detail: Targeted

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Cite this (MGI Cat# 5582463, RRID:MGI:5582463)

Source Database: MGI, catalog # 5582463
Genetic Background: involves: C57BL/6 * SJL
Affected Genes: Runx2
Genomic Alteration: Tg(Col2a1-cre)1Bhr; tm1Javed
Availability: Availability unknown check source stock center
Reference: PMID:21597273
Notes: absent scapula, abnormal limb bone morphology, abnormal long bone epiphyseal plate morphology, abnormal metatarsal bone morphology, abnormal craniofacial bone morphology, decreased birth weight, short ribs, decreased birth body size, respiratory failure, abnormal pelvic girdle bone morphology, neonatal lethality, complete penetrance, absent vertebrae, absent metacarpal bones Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 5792828, RRID:MGI:5792828)

Source Database: MGI, catalog # 5792828
Genetic Background: involves: 129 * C57BL/6
Affected Genes: Fubp1
Genomic Alteration: tm1.1Dlev
Availability: Availability unknown check source stock center
Reference: PMID:26774856
Notes: hemorrhage, absent cerebellar lobules, thin placenta labyrinth, decreased megakaryocyte cell number, decreased B cell number, anemia, abnormal hematopoietic stem cell physiology, abnormal hematopoietic precursor cell number, abnormal definitive hematopoiesis, abnormal blood circulation, abnormal stratification in cerebral cortex, abnormal pulmonary alveolar sac morphology, abnormal placenta morphology, abnormal placenta intervillous maternal lacunae morphology, abnormal brain morphology, thymus hypoplasia, spleen hypoplasia, small lung, impaired branching involved in alveolar sac morphogenesis, decreased bone marrow cell number, cardiac hypertrophy, abnormal cerebral hemisphere morphology, abnormal prenatal body size, decreased fetal size, lymphoid hypoplasia, neonatal lethality, complete penetrance, pale liver, small liver, pulmonary hypoplasia, prenatal lethality, incomplete penetrance, pallor, perinatal lethality, incomplete penetrance, prenatal growth retardation Allele Detail: Targeted

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Cite this (MGI Cat# 3851984, RRID:MGI:3851984)

Source Database: MGI, catalog # 3851984
Genetic Background: involves: 129/Sv * C57BL/6
Affected Genes: Zbtb18
Genomic Alteration: tm1Haok
Availability: Availability unknown check source stock center
Reference: PMID:19409883
Notes: abnormal hippocampus morphology, small hippocampus, neonatal lethality, complete penetrance, increased neuron apoptosis, decreased neuron number, abnormal postnatal subventricular zone morphology, abnormal neuron physiology, abnormal neocortex morphology, abnormal hippocampus pyramidal cell layer, abnormal hippocampus granule cell layer, abnormal cortical ventricular zone morphology, abnormal cerebellar foliation Allele Detail: Targeted

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Cite this (MGI Cat# 2175079, RRID:MGI:2175079)

Source Database: MGI, catalog # 2175079
Genetic Background: involves: 129S/SvEv
Affected Genes: Igf1r
Genomic Alteration: tm1Arge
Availability: Availability unknown check source stock center
Reference: PMID:8402901
Notes: small hair follicles, atelectasis, abnormal hair follicle morphology, translucent skin, decreased hair follicle number, thin epidermis, cyanosis, muscle hypoplasia, thin epidermis stratum spinosum, respiratory failure, abnormal spinal cord morphology, delayed bone ossification, decreased birth weight, abnormal brainstem morphology, neonatal lethality, complete penetrance, decreased oligodendrocyte progenitor number Allele Detail: Targeted

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Cite this (MGI Cat# 2175131, RRID:MGI:2175131)

Source Database: MGI, catalog # 2175131
Genetic Background: involves: 129S1/Sv * C57BL/6
Affected Genes: Myf6
Genomic Alteration: tm1Wb
Availability: Availability unknown check source stock center
Reference: PMID:7588068
Notes: abnormal sternocostal joint morphology, abnormal myotome development, respiratory distress, abnormal rib morphology, neonatal lethality, complete penetrance, abnormal intercostal muscle morphology, rib bifurcation, abnormal sternum ossification, rib fusion, short ribs, truncated ribs, abnormal myotome morphology, abnormal cervical vertebrae morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5301973, RRID:MGI:5301973)

Source Database: MGI, catalog # 5301973
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6
Affected Genes: Lmnb1, Lmnb2
Genomic Alteration: tm1Yxz
Availability: Availability unknown check source stock center
Reference: PMID:22116031
Notes: abnormal neuronal precursor proliferation, increased neuronal precursor cell number, thin diaphragm muscle, respiratory failure, decreased fetal size, abnormal stratification in cerebral cortex, decreased embryo size, neonatal lethality, complete penetrance, thin cerebral cortex, microcephaly, abnormal neuron differentiation, abnormal phrenic nerve innervation pattern to diaphragm, abnormal pulmonary alveolus morphology, abnormal cell physiology, abnormal neuronal migration Allele Detail: Targeted

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Cite this (MGI Cat# 2175049, RRID:MGI:2175049)

Source Database: MGI, catalog # 2175049
Genetic Background: either: (involves: 129S2/SvPas * 129/Sv) or (involves: 129S2/SvPas * BALB/c) or (involves: 129S2/SvPas * C57BL/6)
Affected Genes: Grin1
Genomic Alteration: tm1Stl
Availability: Availability unknown check source stock center
Reference: PMID:8313466
Notes: ataxia, apnea, abnormal suckling behavior, cyanosis, neonatal lethality, complete penetrance, abnormal brainstem morphology, absence of NMDA-mediated synaptic currents Allele Detail: Targeted

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Cite this (MGI Cat# 3701801, RRID:MGI:3701801)

Source Database: MGI, catalog # 3701801
Genetic Background: involves: 129X1/SvJ * C57BL/6
Affected Genes: Ptges3
Genomic Alteration: Gt(W069F07)Wrst
Availability: Availability unknown check source stock center
Reference: PMID:17000766
Notes: atelectasis, small lung, impaired lung alveolus development, abnormal surfactant secretion, decreased type II pneumocyte number, pale lung, abnormal skin appearance, impaired skin barrier function, lethargy, abnormal breathing pattern, neonatal lethality, complete penetrance, shiny skin Allele Detail: Gene trapped

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Cite this (MGI Cat# 2170585, RRID:MGI:2170585)

Source Database: MGI, catalog # 2170585
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Hoxa2, Hoxa1
Genomic Alteration: tm2Mrc; tm1Mrc
Availability: Availability unknown check source stock center
Reference: PMID:10529419
Notes: abnormal hindbrain morphology, abnormal middle ear ossicle morphology, absent outer ear, neonatal lethality, complete penetrance, small middle ear ossicles Allele Detail: Targeted

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Cite this (MGI Cat# 2674287, RRID:MGI:2674287)

Source Database: MGI, catalog # 2674287
Genetic Background: involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6
Affected Genes: Meox1, Meox2
Genomic Alteration: Tg(Mx1-TAX)2627Arnh; tm1Vpa
Availability: Availability unknown check source stock center
Reference: PMID:12925591
Notes: vestigial tail, abnormal somite development, abnormal skeletal muscle morphology, absent vertebrae, absent ribs, decreased body length, neonatal lethality, complete penetrance Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 3818641, RRID:MGI:3818641)

Source Database: MGI, catalog # 3818641
Genetic Background: involves: 101/Rl * C3H/Rl
Affected Genes: Tyr
Genomic Alteration: c-14CoS
Availability: Availability unknown check source stock center
Reference: PMID:7117820
Notes: neonatal lethality, complete penetrance, neonatal lethality, complete penetrance Allele Detail: Radiation induced

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Cite this (MGI Cat# 2451237, RRID:MGI:2451237)

Source Database: MGI, catalog # 2451237
Genetic Background: involves: 129P2/OlaHsd * C57BL
Affected Genes: Arx
Genomic Alteration: tm1Kki
Availability: Availability unknown check source stock center
Reference: PMID:12379852
Notes: neonatal lethality, complete penetrance, abnormal hippocampus CA3 region morphology, abnormal cortical ventricular zone morphology, abnormal cortical plate morphology, abnormal cortical marginal zone morphology, abnormal fetal Leydig cell differentiation, enlarged third ventricle, abnormal corpus callosum morphology, abnormal central medial nucleus morphology, abnormal brain internal capsule morphology, absent hippocampal commissure, abnormal olfactory bulb morphology, abnormal dentate gyrus morphology, small olfactory bulb, small testis, abnormal nervous system tract morphology, abnormal hippocampus development, seminal vesicle hypoplasia, decreased brain size, enlarged seminiferous tubules, abnormal thalamus morphology, abnormal forebrain development, absent hippocampal fimbria, abnormal glutaminergic neuron morphology, abnormal neocortex morphology, abnormal neuronal migration, abnormal telencephalon development, abnormal telencephalon morphology, thin cortical plate Allele Detail: Targeted

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