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on page 1 showing 20 out of 1,301 results from 1 sources

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# 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# 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# 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: abnormal bone ossification, abnormal vitamin D level, alopecia, decreased circulating calcium level, decreased circulating phosphate level, disorganized long bone epiphyseal plate, increased activity of parathyroid, increased osteoid volume, postnatal growth retardation, premature death, weight loss 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: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# 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: Psmc1
Genomic Alteration: Tg(Camk2a-tTA)1Mmay; tm1Maye; Tg(tetO-cre)1Lin
Availability: Availability unknown check source stock center
Reference: PMID:18701681
Notes: postnatal growth retardation, premature death, abnormal eating behavior, abnormal fear/anxiety-related behavior, abnormal spatial learning, thin cerebral cortex, enlarged brain ventricles, loss of cortex neurons, increased neuron apoptosis, neurodegeneration, gliosis, alpha-synuclein inclusion body, forebrain atrophy 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: 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# 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: decreased fibroblast proliferation, decreased double-positive T cell number, postnatal growth retardation, increased susceptibility to fungal infection, abnormal cell cycle checkpoint function 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, abnormal bile salt level, postnatal growth retardation, increased susceptibility to weight loss, enlarged liver, increased circulating aspartate transaminase level, increased circulating bilirubin level, abnormal liver physiology 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:10531444, PMID:7670489, PMID:7885444
Notes: abnormal eye electrophysiology, abnormal retinal outer plexiform layer morphology, short photoreceptor inner segment, abnormal retinal photoreceptor morphology, short photoreceptor outer segment, abnormal retina morphology, increased retinal apoptosis, abnormal retinal rod cell morphology, lethargy, abnormal renal glomerulus basement membrane morphology, albuminuria, fused podocyte foot processes, abnormal miniature endplate potential, abnormal neuromuscular synapse morphology, failure of neuromuscular synapse postsynaptic differentiation, failure of neuromuscular synapse presynaptic differentiation, glomerulonephritis, postnatal growth retardation, postnatal growth retardation, postnatal lethality, complete penetrance, increased urine protein level, increased urine protein level, increased renal glomerulus basement membrane thickness, abnormal glomerular filtration barrier function, decreased total retina thickness 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: 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# 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: alopecia, epidermal hyperplasia, increased salivation, postnatal growth retardation, 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: abnormal tracheal ciliated epithelium morphology, absent respiratory motile cilia, increased respiratory mucosa goblet cell number, postnatal growth retardation, postnatal lethality, complete penetrance, slow postnatal weight gain 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# 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: abnormal long bone epiphysis morphology, abnormal vitamin D level, decreased body weight, decreased white adipose tissue amount, postnatal growth retardation, increased circulating calcium level, increased circulating phosphate level, decreased bone mineral density, premature death 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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