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on page 1 showing 20 out of 1,314 results

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: increased or absent threshold for auditory brainstem response, impaired hearing, abnormal tectorial membrane morphology, enlarged tectorial membrane, sensorineural hearing loss, nonsyndromic hearing loss, increased or absent threshold for auditory brainstem response, impaired hearing, decreased body size, short snout, abnormal nasal bone morphology, abnormal cranium morphology, abnormal chondrocyte morphology, prominent forehead, abnormal articular cartilage morphology, triangular face, postnatal growth retardation, disorganized long bone epiphyseal plate Allele Detail: Targeted

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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: abnormal synaptonemal complex, azoospermia, male infertility, abnormal mammary gland growth during lactation, abnormal male germ cell apoptosis, arrest of male meiosis, abnormal Sertoli cell morphology, azoospermia, postnatal growth retardation, male infertility, wrinkled skin, decreased body size, hunched posture, small testis, decreased male germ cell number, abnormal mammary gland growth during pregnancy, abnormal mammary gland epithelium morphology, abnormal nursing, abnormal spermatocyte morphology, small seminiferous tubules, decreased testis weight, arrest of male meiosis, arrest of spermatogenesis Allele Detail: Targeted

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Cite this (MGI Cat# 5501521, RRID:MGI:5501521)

Source Database: MGI, catalog # 5501521
Genetic Background: involves: C57BL/6 * CBA/JNCrlj * SJL
Affected Genes: Vdr
Genomic Alteration: tm1.1Pcn
Availability: Availability unknown check source stock center
Reference: PMID:23389957
Notes: decreased circulating phosphate level, abnormal bone ossification, abnormal vitamin D level, alopecia, decreased circulating calcium level, disorganized long bone epiphyseal plate, increased activity of parathyroid, weight loss, premature death, increased osteoid volume, postnatal growth retardation Allele Detail: Targeted

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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:16174331, PMID:15056934
Notes: decreased body weight, postnatal growth retardation 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: postnatal growth retardation, decreased osteoclast cell number, decreased B cell number, decreased body weight, osteopetrosis, oxidative stress, premature death, abnormal nervous system physiology, abnormal long term object recognition memory, abnormal cued conditioning behavior, abnormal contextual conditioning behavior, increased insulin sensitivity, decreased circulating insulin level, decreased insulin secretion, hypoglycemia, short femur Allele Detail: Transgenic

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Cite this (MGI Cat# 3606961, RRID:MGI:3606961)

Source Database: MGI, catalog # 3606961
Genetic Background: involves: FVB/N
Affected Genes:
Genomic Alteration: Tg(KRT14-HPV16E7)2304Plam
Availability: Availability unknown check source stock center
Reference: PMID:8627712
Notes: cataract, postnatal growth retardation Allele Detail: Transgenic

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Cite this (MGI Cat# 3809773, RRID:MGI:3809773)

Source Database: MGI, catalog # 3809773
Genetic Background: involves: 129 * C57BL/6 * CD-1
Affected Genes: Tg(Camk2a-tTA)1Mmay, Psmc1
Genomic Alteration: tm1Maye; Tg(Camk2a-tTA)1Mmay; Tg(tetO-cre)1Lin
Availability: Availability unknown check source stock center
Reference: PMID:18701681
Notes: alpha-synuclein inclusion body, neurodegeneration, increased neuron apoptosis, abnormal fear/anxiety-related behavior, abnormal spatial learning, thin cerebral cortex, enlarged brain ventricles, loss of cortex neurons, forebrain atrophy, postnatal growth retardation, premature death, abnormal eating behavior, gliosis Allele Detail: Targeted, Transgenic

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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: decreased total body fat amount, retinal neovascularization, thick epidermis, decreased insulin secretion, decreased trabecular bone thickness, decreased oxygen consumption, oliguria, decreased tidal volume, decreased hair follicle number, decreased food intake, decreased body mass index, decreased body size, decreased body weight, decreased subcutaneous adipose tissue amount, abnormal optic nerve morphology, premature death, demyelination, abnormal respiratory function, abnormal muscle fiber morphology, abnormal mitochondrion morphology, abnormal glucose homeostasis, abnormal defecation, abnormal coat/hair pigmentation, small thoracic cavity, abnormal myocardium layer morphology, decreased bone mineral density, premature aging, decreased fluid intake, corneal opacity, blindness, axon degeneration, impaired glucose tolerance, increased insulin sensitivity, kyphosis, lordosis, muscle degeneration, exophthalmos, prominent ears, abnormal respiratory electron transport chain, neurodegeneration, postnatal growth retardation 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 pancreas morphology, brain atrophy, cerebellum atrophy, decreased brain size, progressive muscle weakness, Purkinje cell axonal dystrophy, abnormal cerebellum white matter morphology, thick skin, premature death, lysosomal protein accumulation, brain inflammation, astrocytosis, abnormal spine curvature, abnormal cognition, Purkinje cell degeneration, prenatal lethality, incomplete penetrance, penis prolapse, limb grasping, impaired coordination, small nasal bridge, decreased body size, decreased survivor rate, flattened snout, kyphosis, postnatal growth retardation, 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 fertility/fecundity, abnormal skin turgor, demyelination, axonal spheroids, abnormal pancreatic acinar cell morphology, abnormal skeleton morphology, abnormal facial morphology, abnormal gait, ataxia Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3038826, RRID:MGI:3038826)

Source Database: MGI, catalog # 3038826
Genetic Background: B6.129X1-Psme3
Affected Genes: Psme3
Genomic Alteration: tm1Jjm
Availability: Availability unknown check source stock center
Reference: PMID:15004203
Notes: abnormal cell cycle checkpoint function, increased susceptibility to fungal infection, postnatal growth retardation, decreased fibroblast proliferation, decreased double-positive T cell number Allele Detail: Targeted

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Cite this (MGI Cat# 3043817, RRID:MGI:3043817)

Source Database: MGI, catalog # 3043817
Genetic Background: involves: 129S1/SvImJ * 129S4/SvJae
Affected Genes: Atp8b1
Genomic Alteration: tm1Nbf
Availability: Availability unknown check source stock center
Reference: PMID:14976163
Notes: abnormal bile secretion, postnatal growth retardation, abnormal liver physiology, increased circulating bilirubin level, increased circulating aspartate transaminase level, abnormal bile salt level, enlarged liver, increased susceptibility to weight loss Allele Detail: Targeted

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Cite this (MGI Cat# 2175097, RRID:MGI:2175097)

Source Database: MGI, catalog # 2175097
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Lamb2
Genomic Alteration: tm1Jrs
Availability: Availability unknown check source stock center
Reference: PMID:7670489, PMID:10531444, PMID:7885444
Notes: abnormal glomerular filtration barrier function, abnormal miniature endplate potential, increased urine protein level, postnatal lethality, complete penetrance, postnatal growth retardation, glomerulonephritis, failure of neuromuscular synapse presynaptic differentiation, failure of neuromuscular synapse postsynaptic differentiation, abnormal neuromuscular synapse morphology, fused podocyte foot processes, increased retinal apoptosis, abnormal retina morphology, abnormal retinal rod cell morphology, abnormal retinal outer plexiform layer morphology, abnormal retinal photoreceptor morphology, lethargy, decreased total retina thickness, abnormal eye electrophysiology, short photoreceptor inner segment, short photoreceptor outer segment, postnatal growth retardation, increased renal glomerulus basement membrane thickness, increased urine protein level, abnormal renal glomerulus basement membrane morphology, albuminuria Allele Detail: Targeted

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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: postnatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, binucleate, polyploidy, embryonic lethality during organogenesis, incomplete penetrance, decreased birth weight, chromosomal instability, postnatal growth retardation, perinatal lethality, incomplete penetrance, aneuploidy, abnormal mitosis, lethality throughout fetal growth and development, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 2174838, RRID:MGI:2174838)

Source Database: MGI, catalog # 2174838
Genetic Background: Not Specified
Affected Genes:
Genomic Alteration: Tg(FGF7)29Efu
Availability: Availability unknown check source stock center
Reference: PMID:7681397
Notes: postnatal growth retardation, epidermal hyperplasia, alopecia, increased salivation, infertility Allele Detail: Transgenic

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Cite this (MGI Cat# 5796391, RRID:MGI:5796391)

Source Database: MGI, catalog # 5796391
Genetic Background: involves: C57BL/6N
Affected Genes: Gmnc
Genomic Alteration: tm1a(KOMP)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:26882546
Notes: postnatal growth retardation, postnatal lethality, complete penetrance, increased respiratory mucosa goblet cell number, slow postnatal weight gain, abnormal tracheal ciliated epithelium morphology, absent respiratory motile cilia 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 body length, abnormal cartilage morphology, decreased width of hypertrophic chondrocyte zone, decreased body weight, disproportionate dwarf, postnatal growth retardation, decreased long bone epiphyseal plate size, decreased cranium height, postnatal lethality, incomplete penetrance, abnormal long bone epiphyseal plate proliferative zone, abnormal vertebral epiphyseal plate morphology Allele Detail: Targeted

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Cite this (MGI Cat# 2684468, RRID:MGI:2684468)

Source Database: MGI, catalog # 2684468
Genetic Background: Not Specified
Affected Genes: Kl
Genomic Alteration: tm1Yin
Availability: Availability unknown check source stock center
Reference: PMID:14528024
Notes: increased circulating calcium level, decreased body weight, abnormal vitamin D level, increased circulating phosphate level, decreased bone mineral density, postnatal growth retardation, abnormal long bone epiphysis morphology, decreased white adipose tissue amount, premature death Allele Detail: Targeted

  • From Current Category

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: behavior/neurological phenotype, postnatal growth retardation, postnatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 3045795, RRID:MGI:3045795)

Source Database: MGI, catalog # 3045795
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * FVB * NMRI
Affected Genes: Pax6
Genomic Alteration: tm2Pgr; tm1Pgr; Tg(Pax6-cre,GFP)1Pgr
Availability: Availability unknown check source stock center
Reference: PMID:15110714, PMID:11069887
Notes: absent optic placodes, postnatal growth retardation, postnatal lethality, complete penetrance, decreased pancreatic alpha cell number, decreased pancreatic beta cell number, decreased circulating insulin level, hyperglycemia, increased circulating ketone body level, abnormal optic vesicle formation, abnormal optic cup morphology Allele Detail: Targeted, Transgenic

  • From Current Category

Cite this (MGI Cat# 3578659, RRID:MGI:3578659)

Source Database: MGI, catalog # 3578659
Genetic Background: involves: 129S6/SvEvBrd * 129S6.129S4-Slc11a2
Affected Genes: Hfe, Slc11a2
Genomic Alteration: tm2Nca; tm1Nca
Availability: Availability unknown check source stock center
Reference: PMID:15849611
Notes: increased liver iron level, mortality/aging, decreased hematocrit, postnatal growth retardation Allele Detail: Targeted

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