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Integrated: Animals

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Phenotype:neonatal lethality, complete penetrance (facet)


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Database Proper Citation Species Name Phenotype Availability Reference Notes Affected Gene Genomic Alteration Catalog ID Background
MGIRRID:MGI:3723640Mus musculusPax9tm1.1Hpt/Pax9tm1.1Hpt; Tg(Pgk1-cre)1Lniabnormal thymus lobule morphology, absent parathyroid glands, absent premaxilla, aphagia, cleft secondary palate, abnormal maxillary shelf morphology, neonatal lethality, complete penetrance, polydactyly, absent teeth, absent mandibular coronoid process, abnormal tympanic ring morphology, abnormal palatine bone horizontal plate morphologyAvailability unknown check source stock centerPMID:17610273Allele Detail: Targeted, TransgenicTg(Pgk1-cre)1Lni, Pax9tm1.1Hpt; Tg(Pgk1-cre)1Lni3723640involves: 129S2/SvPas * BALB/c * C57BL/6 * SJL
MGIRRID:MGI:2175079Mus musculusIgf1rtm1Arge/Igf1rtm1Argeabnormal brainstem morphology, decreased birth weight, neonatal lethality, complete penetrance, respiratory failure, muscle hypoplasia, delayed bone ossification, abnormal spinal cord morphology, translucent skin, decreased hair follicle number, thin epidermis stratum spinosum, small hair follicles, decreased oligodendrocyte progenitor number, cyanosis, atelectasis, abnormal hair follicle morphology, thin epidermisAvailability unknown check source stock centerPMID:8402901Allele Detail: TargetedIgf1rtm1Arge2175079involves: 129S/SvEv
MGIRRID:MGI:6314225Mus musculusAtp1a2tm1.1Tmklh/Atp1a2tm1.1Tmklhabnormal hippocampus physiology, neonatal lethality, complete penetranceAvailability unknown check source stock centerPMID:26911348Allele Detail: TargetedAtp1a2tm1.1Tmklh6314225involves: 129S1/Sv * C57BL/6J
MGIRRID:MGI:2175131Mus musculusMyf6tm1Wb/Myf6tm1Wbrib bifurcation, abnormal cervical vertebrae morphology, respiratory distress, abnormal myotome morphology, abnormal intercostal muscle morphology, abnormal myotome development, abnormal sternum ossification, short ribs, neonatal lethality, complete penetrance, truncated ribs, abnormal sternocostal joint morphology, abnormal rib morphology, rib fusionAvailability unknown check source stock centerPMID:7588068Allele Detail: TargetedMyf6tm1Wb2175131involves: 129S1/Sv * C57BL/6
MGIRRID:MGI:3521928Mus musculusFoxg1tm1(cre)Skm/Foxg1+; Top2btm2Jcw/Top2btm2.1Jcwrespiratory failure, abnormal motor capabilities/coordination/movement, abnormal hippocampus granule cell layer, abnormal hippocampus morphology, small olfactory bulb, atelectasis, abnormal hippocampus pyramidal cell layer, neonatal lethality, complete penetrance, abnormal cerebral cortex morphologyAvailability unknown check source stock centerPMID:12773624Allele Detail: TargetedTop2b, Foxg1tm2Jcw; tm2.1Jcw; tm1(cre)Skm3521928involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ
MGIRRID:MGI:6150914Mus musculusTg(Sp7-tTA/tetO-EGFP/cre)1Amc; Rnf146tm1.1Rtpl/Rnf146tm1.1Rtpldecreased compact bone thickness, decreased bone ossification, decreased circulating insulin level, decreased osteoblast cell number, decreased osteoblast proliferation, impaired glucose tolerance, increased total body fat amount, increased bone marrow adipose tissue amount, decreased pancreatic islet number, decreased insulin secretion, increased circulating glucose level, abnormal circulating osteocalcin level, increased circulating triglyceride level, clavicle hypoplasia, skeleton phenotype, respiratory distress, neonatal lethality, complete penetrance, large posterior fontanelle, large anterior fontanelle, increased bone trabecular spacing, impaired osteoblast differentiation, decreased trabecular bone volume, decreased compact bone volume, decreased bone trabecula number, decreased bone mineralization, decreased bone mineral density, small pancreatic islets, abnormal rib morphology, abnormal limb long bone morphology, abnormal intramembranous bone ossification, abnormal endochondral bone ossification, abnormal ameloblast differentiation, abnormal alveolar process morphologyAvailability unknown check source stock centerPMID:28581440Allele Detail: Targeted, TransgenicRnf146tm1.1Rtpl; Tg(Sp7-tTA,tetO-EGFP/cre)1Amc6150914involves: C57BL/6J * CD-1
MGIRRID:MGI:3687545Mus musculusShhtm2Chg/Shhtm2Chgneonatal lethality, complete penetranceAvailability unknown check source stock centerPMID:16611729Allele Detail: TargetedShhtm2Chg3687545involves: 129S1/Sv * 129X1/SvJ
MGIRRID:MGI:3722142Mus musculusHoxb2tm1Fmr/Hoxb2tm1Fmr; Hoxa2tm1Ipc/Hoxa2tm1Ipcincreased rhombomere 1 size, abnormal rhombomere morphology, neonatal lethality, complete penetranceAvailability unknown check source stock centerPMID:10230789Allele Detail: TargetedHoxa2, Hoxb2tm1Fmr; tm1Ipc3722142involves: 129/Sv * 129S2/SvPas
MGIRRID:MGI:3510314Mus musculusTbx1tm1.1Dsr/Tbx1tm1.1Dsranotia, right aortic arch, small cricoid cartilage, double outlet right ventricle, athymia, cleft secondary palate, palatal shelves fail to meet at midline, abnormal middle ear ossicle morphology, aberrant origin of the right subclavian artery, persistent truncus arteriosis, double aortic arch, fusion of basioccipital and basisphenoid bone, abnormal inner ear morphology, abnormal hyoid bone morphology, decreased tympanic ring size, neonatal lethality, complete penetrance, ventricular septal defect, abnormal stapes morphologyAvailability unknown check source stock centerPMID:15469978Allele Detail: TargetedTbx1tm1.1Dsr3510314either: 129/Sv or (involves: 129/Sv * C57BL/6)
MGIRRID:MGI:5301973Mus musculusLmnb1tm1Yxz/Lmnb1tm1Yxz; Lmnb2tm1Yxz/Lmnb2tm1Yxzmicrocephaly, thin cerebral cortex, decreased embryo size, neonatal lethality, complete penetrance, abnormal pulmonary alveolus morphology, decreased fetal size, abnormal cell physiology, respiratory failure, thin diaphragm muscle, abnormal phrenic nerve innervation pattern to diaphragm, abnormal neuron differentiation, abnormal neuronal migration, abnormal neuronal precursor proliferation, abnormal stratification in cerebral cortex, increased neuronal precursor cell numberAvailability unknown check source stock centerPMID:22116031Allele Detail: TargetedLmnb2, Lmnb1tm1Yxz5301973involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6
MGIRRID:MGI:3773315Mus musculusPbx3tm1.1Og/Pbx3tm1.1Ogneonatal lethality, complete penetrance, cyanosisAvailability unknown check source stock centerPMID:18155191Allele Detail: TargetedPbx3tm1.1Og3773315involves: 129S4/SvJae * C57BL/6
MGIRRID:MGI:2175049Mus musculusGrin1tm1Stl/Grin1tm1Stlapnea, neonatal lethality, complete penetrance, cyanosis, absence of NMDA-mediated synaptic currents, abnormal brainstem morphology, ataxia, abnormal suckling behaviorAvailability unknown check source stock centerPMID:8313466Allele Detail: TargetedGrin1tm1Stl2175049either: (involves: 129S2/SvPas * 129/Sv) or (involves: 129S2/SvPas * BALB/c) or (involves: 129S2/SvPas * C57BL/6)
MGIRRID:MGI:3701801Mus musculusPtges3Gt(W069F07)Wrst/Ptges3Gt(W069F07)Wrstdecreased type II pneumocyte number, abnormal breathing pattern, abnormal surfactant secretion, atelectasis, lethargy, impaired skin barrier function, abnormal skin appearance, neonatal lethality, complete penetrance, shiny skin, small lung, impaired lung alveolus development, pale lungAvailability unknown check source stock centerPMID:17000766Allele Detail: Gene trappedPtges3Gt(W069F07)Wrst3701801involves: 129X1/SvJ * C57BL/6
MGIRRID:MGI:3575015Mus musculusMycntm1Psk/Mycntm1Psk; Tg(Sftpc-cre)1Blhabnormal pulmonary alveolus epithelial cell morphology, abnormal lung morphology, abnormal lung epithelium morphology, decreased type I pneumocyte number, abnormal branching involved in lung morphogenesis, abnormal lung development, neonatal lethality, complete penetrance, decreased type II pneumocyte numberAvailability unknown check source stock centerPMID:15716345Allele Detail: Targeted, TransgenicMycntm1Psk; Tg(Sftpc-cre)1Blh3575015involves: 129 * C57BL/6 * ICR
MGIRRID:MGI:3718028Mus musculusAldh1a3tm1Gdu/Aldh1a3tm1Gduneonatal lethality, complete penetrance, abnormal vitreous body morphology, increased total retina thickness, persistent hyperplastic primary vitreousAvailability unknown check source stock centerReferences (2)Allele Detail: TargetedAldh1a3tm1Gdu3718028involves: C57BL/6
MGIRRID:MGI:2170585Mus musculusHoxa1tm2Mrc/Hoxa1tm2Mrc; Hoxa2tm1Mrc/Hoxa2tm1Mrcabsent outer ear, small middle ear ossicles, abnormal hindbrain morphology, neonatal lethality, complete penetrance, abnormal middle ear ossicle morphologyAvailability unknown check source stock centerPMID:10529419Allele Detail: TargetedHoxa2, Hoxa1tm2Mrc; tm1Mrc2170585involves: 129S1/Sv * 129X1/SvJ
MGIRRID:MGI:4881709Mus musculusSsr3tm1Ryn/Ssr3tm1Ryndecreased placental labyrinth size, fetal growth retardation, neonatal lethality, complete penetrance, decreased fetal weight, abnormal placental labyrinth vasculature morphology, small placenta, decreased placenta weight, abnormal placenta physiology, increased placenta apoptosis, abnormal placenta vasculature, abnormal pulmonary alveolus morphology, abnormal placenta morphologyAvailability unknown check source stock centerPMID:21246656Allele Detail: TargetedSsr3tm1Ryn4881709involves: C57BL/6 * CBA
MGIRRID:MGI:4844107Mus musculusDel(11Stat5a-Stat5b)1Mam/Del(11Stat5a-Stat5b)1Mamdecreased mean corpuscular hemoglobin, neonatal lethality, complete penetrance, decreased hematocrit, hypochromic microcytic anemiaAvailability unknown check source stock centerPMID:18552213Allele Detail: TargetedDel(11Stat5a-Stat5b)1MamDel(11Stat5a-Stat5b)1Mam4844107involves: 129S6/SvEvTac * FVB/N
MGIRRID:MGI:3771865Mus musculusFgfrl1tm1True/Fgfrl1tm1Trueincreased kidney apoptosis, neonatal lethality, complete penetrance, absent kidney, abnormal metanephric mesenchyme morphology, decreased kidney cell proliferation, thin diaphragm muscle, small cranium, homeostasis/metabolism phenotype, absent nephron, decreased length of long bones, absent metanephros, absent metanephros, muscle hypoplasia, abnormal neurocranium morphology, skeleton phenotype, thin diaphragm muscle, diaphragmatic hernia, cyanosis, abnormal diaphragm development, respiratory distress, abnormal nephrogenic mesenchyme morphogenesis, abnormal metanephros morphology, abnormal kidney development, impaired branching involved in ureteric bud morphogenesis, domed cranium, respiratory system phenotype, no spontaneous movementAvailability unknown check source stock centerReferences (4)Allele Detail: TargetedFgfrl1tm1True3771865B6.129S6-Fgfrl1
MGIRRID:MGI:2674287Mus musculusMeox2tm1Vpa/Meox2tm1Vpa; Meox1Tg(Mx1-TAX)2627Arnh/Meox1Tg(Mx1-TAX)2627Arnhabsent ribs, vestigial tail, abnormal somite development, decreased body length, abnormal skeletal muscle morphology, absent vertebrae, neonatal lethality, complete penetranceAvailability unknown check source stock centerPMID:12925591Allele Detail: Targeted, TransgenicMeox1, Meox2Tg(Mx1-TAX)2627Arnh; tm1Vpa2674287involves: 129P2/OlaHsd * C3H/HeJ * C57BL/6
MGIRRID:MGI:3586912Mus musculusTbx1tm1Pa/Tbx1tm1Paabnormal cranium morphology, absent second pharyngeal arch, abnormal middle ear ossicle morphology, abnormal tympanic ring morphology, abnormal ear shape, abnormal upper incisor morphology, short neck, abnormal thymus development, neonatal lethality, complete penetrance, athymia, decreased embryo size, respiratory failure, hydrops fetalis, abnormal pharyngeal pouch morphology, pharynx stenosis, absent parathyroid glands, abnormal zygomatic arch morphology, small thyroid cartilage, absent mandibular coronoid process, fusion of basioccipital and basisphenoid bone, small otic vesicle, abnormal fourth pharyngeal arch morphology, abnormal third pharyngeal arch morphology, double aortic arch, absent arcus anterior, cleft secondary palate, abnormal cervical atlas morphology, short mandible, small cricoid cartilage, persistent truncus arteriosis, abnormal palatal shelf fusion at midline, micrognathia, absent outer ear, right aortic arch, abnormal pharyngeal arch artery morphology, abnormal pharyngeal arch morphology, abnormal facial morphology, lowered ear position, abnormal temporal bone morphology, abnormal semicircular canal morphology, absent upper incisorsAvailability unknown check source stock centerPMID:11242110Allele Detail: TargetedTbx1tm1Pa3586912either: (involves: 129) or (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * Swiss Webster)
MGIRRID:MGI:3818641Mus musculusTyrc-14CoS/Tyrc-14CoSneonatal lethality, complete penetrance, neonatal lethality, complete penetranceAvailability unknown check source stock centerPMID:7117820Allele Detail: Radiation inducedTyrc-14CoS3818641involves: 101/Rl * C3H/Rl
MGIRRID:MGI:2451237Mus musculusArxtm1Kkiabnormal glutaminergic neuron morphology, abnormal thalamus morphology, neonatal lethality, complete penetrance, absent hippocampal commissure, enlarged seminiferous tubules, small olfactory bulb, enlarged third ventricle, decreased brain size, abnormal olfactory bulb morphology, abnormal hippocampus development, abnormal neuronal migration, abnormal telencephalon development, abnormal fetal Leydig cell differentiation, abnormal cortical marginal zone morphology, small testis, abnormal cortical plate morphology, abnormal central medial nucleus morphology, seminal vesicle hypoplasia, absent hippocampal fimbria, abnormal hippocampus CA3 region morphology, abnormal neocortex morphology, abnormal brain internal capsule morphology, thin cortical plate, abnormal cortical ventricular zone morphology, abnormal corpus callosum morphology, abnormal dentate gyrus morphology, abnormal telencephalon morphology, abnormal forebrain development, abnormal nervous system tract morphologyAvailability unknown check source stock centerPMID:12379852Allele Detail: TargetedArxtm1Kki2451237involves: 129P2/OlaHsd * C57BL
MGIRRID:MGI:3052107Mus musculusShhtm1Ptch/Shhtm1Ptchdecreased embryo size, abnormal spinal cord interneuron morphology, oligodactyly, neonatal lethality, complete penetrance, decreased motor neuron number, holoprosencephalyAvailability unknown check source stock centerPMID:15075292Allele Detail: TargetedShhtm1Ptch3052107involves: 129P2/OlaHsd * FVB/N * various
MGIRRID:MGI:3053046Mus musculusNfkbiatm1Bal/Nfkbiatm1Bal; Nfkbietm1Syme/Nfkbietm1Symeneonatal lethality, complete penetrance, decreased pre-B cell number, decreased immature B cell number, increased B cell apoptosis, abnormal T cell differentiation, abnormal B cell differentiation, increased T cell apoptosisAvailability unknown check source stock centerPMID:14665694Allele Detail: TargetedNfkbia, Nfkbietm1Bal; tm1Syme3053046involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2
MGIRRID:MGI:6241488Mus musculusH2afvTg(Wnt1-cre)11Rth/H2afv+; Resttm1.1Yasu/Resttm1.1Yasuneonatal lethality, complete penetrance, nervous system phenotypeAvailability unknown check source stock centerPMID:25818501Allele Detail: Targeted, TransgenicRest, H2afvtm1.1Yasu; Tg(Wnt1-cre)11Rth6241488involves: 129S4/SvJae * C57BL/6 * C57BL/6J * CBA/J
MGIRRID:MGI:3037948Mus musculusDgat2tm1Far/Dgat2tm1Fardecreased circulating triglyceride level, decreased fatty acid level, decreased unsaturated fatty acid level, abnormal lipid level, orthokeratosis, decreased triglyceride level, decreased circulating free fatty acid level, decreased body surface temperature, dehydration, weight loss, decreased birth weight, decreased body size, tight skin, dry skin, neonatal lethality, complete penetrance, shiny skin, abnormal suckling behavior, decreased body length, decreased glycogen level, abnormal phospholipid level, tail necrosis, abnormal epidermal layer morphology, abnormal epidermal lamellar body morphology, hypoglycemia, impaired skin barrier function, decreased fetal weight, thin epidermisAvailability unknown check source stock centerPMID:14668353Allele Detail: TargetedDgat2tm1Far3037948involves: 129S4/SvJae * C57BL/6J
MGIRRID:MGI:5470528Mus musculusRobo2tm1Mrt/Robo2tm1Mrt; Robo1tm1Matl/Robo1tm1Matlabnormal foregut morphology, absent gastric milk in neonates, abnormal stomach position or orientation, abnormal diaphragm morphology, abnormal spinal cord ventral commissure morphology, abnormal dorsal aorta morphology, small esophagus, esophagus hypoplasia, abnormal olfactory tract morphology, abnormal axon guidance, decreased cell migration, short trachea, neonatal lethality, complete penetrance, cyanosis, respiratory failureAvailability unknown check source stock centerReferences (3)Allele Detail: TargetedRobo1, Robo2tm1Matl; tm1Mrt5470528involves: 129P2/OlaHsd
MGIRRID:MGI:3653597Mus musculusTg(Col2a1-cre)1Asz; Ilktm3Ref/Ilktm3Refdisproportionate dwarf, decreased cell proliferation, disorganized long bone epiphyseal plate, abnormal chest morphology, decreased fetal size, neonatal lethality, complete penetrance, abnormal cell adhesion, abnormal cell cycle, decreased long bone epiphyseal plate size, abnormal long bone hypertrophic chondrocyte zone, cleft palate, pulmonary hypoplasiaAvailability unknown check source stock centerPMID:12671688Allele Detail: Transgenic, TargetedIlktm3Ref; Tg(Col2a1-cre)1Asz3653597involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
MGIRRID:MGI:3703795Mus musculusMan1a2tm1.1Ahe/Man1a2tm1.1Aheabnormal lung development, thick pulmonary interalveolar septum, pulmonary alveolar hemorrhage, neonatal lethality, complete penetrance, abnormal pulmonary alveolus morphology, respiratory distress, atelectasis, cyanosisAvailability unknown check source stock centerPMID:17121831Allele Detail: TargetedMan1a2tm1.1Ahe3703795involves: 129S4/SvJae * C57BL/6
MGIRRID:MGI:4439274Mus musculusHs2st1tm1.2Je/Hs2st1tm1.2Jeneonatal lethality, complete penetrance, absent kidneyAvailability unknown check source stock centerPMID:19889634Allele Detail: TargetedHs2st1tm1.2Je4439274involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J
MGIRRID:MGI:3833924Mus musculusEif2s1tm1Rjk/Eif2s1tm1Rjk; Ppp1r15btm1Dron/Ppp1r15btm1Dronneonatal lethality, complete penetrance, decreased fetal weight, hypoglycemia, decreased erythrocyte cell numberAvailability unknown check source stock centerPMID:19181853Allele Detail: TargetedPpp1r15b, Eif2s1tm1Dron; tm1Rjk3833924involves: 129P2/OlaHsd
MGIRRID:MGI:5289695Mus musculusLrp4tm2Her/Lrp4tm2Herneonatal lethality, complete penetrance, abnormal ureteric bud invasion, abnormal kidney development, impaired branching involved in ureteric bud morphogenesis, absent kidney, single kidney, absent metanephric mesenchyme, abnormal ureteric bud morphology, ureter hypoplasia, abnormal neuromuscular synapse morphologyAvailability unknown check source stock centerPMID:20454682Allele Detail: TargetedLrp4tm2Her5289695involves: 129S/SvEv * C57BL
MGIRRID:MGI:3796144Mus musculusMirc1tm1.2Tyj/Mirc1tm1.2Tyjabnormal B cell differentiation, decreased embryo weight, decreased pre-B cell number, neonatal lethality, complete penetrance, pulmonary hypoplasia, decreased embryo size, abnormal interventricular septum morphology, increased B cell apoptosisAvailability unknown check source stock centerPMID:18329372Allele Detail: TargetedMirc1tm1.2Tyj3796144involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL
MGIRRID:MGI:4360342Mus musculusCdkn1atm1Led/Cdkn1atm1Led; Brca1tm2.1Cxd/Brca1tm2.1Cxdneonatal lethality, complete penetranceAvailability unknown check source stock centerPMID:12533509Allele Detail: TargetedBrca1, Cdkn1atm1Led; tm2.1Cxd4360342involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB
MGIRRID:MGI:5494467Mus musculusImpad1Gt(RST634)Byg/Impad1Gt(RST634)Byg; Papss2bm/Papss2bmabnormal thoracic cage morphology, short ulna, short sternum, disorganized long bone epiphyseal plate, shortened head, short ribs, short radius, short humerus, short limbs, neonatal lethality, complete penetrance, axial skeleton hypoplasia, short scapula, abnormal cartilage developmentAvailability unknown check source stock centerPMID:23479625Allele Detail: Spontaneous, Gene trappedImpad1, Papss2bm; Gt(RST634)Byg5494467involves: 129P2/OlaHsd * LDJ/Le
MGIRRID:MGI:3588431Mus musculusGdnftm1Lmgd/Gdnftm1Lmgdabnormal enteric cholinergic neuron morphology, impaired branching involved in ureteric bud morphogenesis, intestinal hypoperistalsis, absent enteric neurons, absent ureteric bud, abnormal kidney development, neonatal lethality, complete penetrance, absent kidneyAvailability unknown check source stock centerPMID:8657307Allele Detail: TargetedGdnftm1Lmgd3588431either: (involves: 129S4/SvJae) or (involves: 129S1/Sv * 129X1/SvJ)
MGIRRID:MGI:5518952Mus musculusGata3tm1.1Gan/Gata3tm1.1Gan; Tg(Pax2-cre)1Akgabnormal vestibular ganglion morphology, decreased organ of Corti supporting cell number, decreased cochlear hair cell number, decreased cochlear coiling, neonatal lethality, complete penetrance, cochlear ganglion degeneration, absent cochlear hair cells, abnormal cochlea morphology, abnormal cochlear ganglion morphology, abnormal cochlear hair cell morphology, abnormal crista ampullaris morphology, abnormal inner ear development, abnormal organ of Corti morphology, inner ear hypoplasia, increased apoptosisAvailability unknown check source stock centerPMID:23666531Allele Detail: Transgenic, TargetedGata3tm1.1Gan; Tg(Pax2-cre)1Akg5518952involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6Ncr
MGIRRID:MGI:5466151Mus musculusHspa5baffled/Hspa5baffledabnormal neuron proliferation, abnormal stratification in cerebral cortex, abnormal cerebellum morphology, forebrain hypoplasia, nervous system phenotype, respiratory failure, abnormal cortical intermediate zone morphology, abnormal axon morphology, abnormal axon extension, abnormal cerebral cortex morphology, abnormal neuron differentiation, abnormal brain internal capsule morphology, abnormal axon fasciculation, decreased body size, abnormal corpus callosum morphology, neonatal lethality, complete penetrance, abnormal brain white matter morphology, decreased surfactant secretionAvailability unknown check source stock centerPMID:22821687Allele Detail: Chemically induced (ENU)Hspa5baffled5466151FVB.Cg-Hspa5
MGIRRID:MGI:3706969Mus musculusRbpjtm1Hon/Rbpjtm1Hon; Pax3tm1(cre)Joe/Pax3+loss of GABAergic neurons, abnormal neural tube morphology, abnormal intercostal muscle morphology, abnormal epaxial muscle morphology, abnormal diaphragm morphology, respiratory failure, no spontaneous movement, abnormal neuron differentiation, neonatal lethality, complete penetrance, hypaxial muscle hypoplasia, decreased satellite cell number, decreased neuronal precursor cell number, abnormal spinal cord interneuron morphology, abnormal glutaminergic neuron morphology, abnormal myogenesisAvailability unknown check source stock centerReferences (2)Allele Detail: TargetedPax3, Rbpjtm1(cre)Joe; tm1Hon3706969involves: 129P2/OlaHsd
MGIRRID:MGI:5523682Mus musculusNotch2tm3Grid/Notch2tm3Grid; Tg(Pax3-cre)1Joe; Notch1tm6.1Rko/Notch1tm6.1Rkoneonatal lethality, complete penetrance, renal hypoplasiaAvailability unknown check source stock centerPMID:23806616Allele Detail: Targeted, TransgenicNotch2, Notch1Tg(Pax3-cre)1Joe; tm3Grid; tm6.1Rko5523682involves: 129S1/Sv * C57BL/6 * SJL
MGIRRID:MGI:4949907Mus musculusAdgra2tm1.2Bstc/Adgra2tm1.2Bstcabnormal pallium development, abnormal blood-brain barrier function, abnormal blood-cerebrospinal fluid barrier function, abnormal lateral ventricle morphology, perinatal lethality, complete penetrance, hydrocephaly, intracranial hemorrhage, intraventricular hemorrhage, abnormal blood vessel morphology, neonatal lethality, complete penetrance, spinal hemorrhage, abnormal vascular branching morphogenesis, abnormal brain vasculature morphology, enlarged lateral ventricles, abnormal telencephalon development, abnormal telencephalon morphologyAvailability unknown check source stock centerPMID:21421844Allele Detail: TargetedAdgra2tm1.2Bstc4949907B6.Cg-Adgra2
MGIRRID:MGI:3717123Mus musculusZfand5Gt(ROSA)72Sor/Zfand5Gt(ROSA)72Sorabnormal neurocranium morphology, internal hemorrhage, vascular smooth muscle hypoplasia, hemorrhage, asymmetric sternocostal joints, abnormal blood vessel morphology, abnormal sternum morphology, abnormal skeleton morphology, abnormal frontal bone morphology, decreased fibroblast cell migration, neonatal lethality, complete penetrance, respiratory distress, pulmonary edemaAvailability unknown check source stock centerPMID:17143286Allele Detail: Gene trappedZfand5Gt(ROSA)72Sor3717123involves: 129S4/SvJaeSor
MGIRRID:MGI:5588821Mus musculusTshz1tm1Garr/Tshz1tm2.2Garrabnormal olfactory bulb granule cell layer morphology, neonatal lethality, complete penetranceAvailability unknown check source stock centerPMID:24487590Allele Detail: TargetedTshz1tm2.2Garr; tm1Garr5588821mixed
MGIRRID:MGI:3055716Mus musculusNeurod6tm1(cre)Kan/Neurod6+; Gt(ROSA)26Sortm1(DTA)Riet/Gt(ROSA)26Sor+abnormal cerebral cortex morphology, neonatal lethality, complete penetranceAvailability unknown check source stock centerPMID:15314171Allele Detail: TargetedGt(ROSA)26Sor, Neurod6tm1(cre)Kan; tm1(DTA)Riet3055716involves: 129P2/OlaHsd
MGIRRID:MGI:2672849Mus musculusKcnq2tm1Hsa/Kcnq2tm1Hsanervous system phenotype, atelectasis, neonatal lethality, complete penetranceAvailability unknown check source stock centerPMID:10854243Allele Detail: TargetedKcnq2tm1Hsa2672849involves: 129P2/OlaHsd * C57BL/6
MGIRRID:MGI:2176951Mus musculusGja1tm1Kdr/Gja1tm1Kdrabnormal trabecula carnea morphology, edema, abnormal cardiac outflow tract development, abnormal heart right ventricle outflow tract morphology, abnormal breathing pattern, abnormal pulmonary valve morphology, cyanosis, abnormal pulmonary gas exchange, abnormal vascular smooth muscle physiology, neonatal lethality, complete penetranceAvailability unknown check source stock centerReferences (2)Allele Detail: TargetedGja1tm1Kdr2176951involves: 129S1/Sv * 129X1/SvJ
MGIRRID:MGI:4359264Mus musculuspad/padabnormal rib morphology, neonatal lethality, complete penetrance, abnormal intestine morphology, small maxilla, cleft palate, short limbs, shortened head, abnormal vertebral column morphology, small mandible, chondrodystrophy, decreased basicranium angle, abnormal long bone epiphyseal plate proliferative zone, abnormal epiphyseal plate morphology, small mandibleAvailability unknown check source stock centerPMID:7183705Allele Detail: Spontaneouspad4359264Not Specified
MGIRRID:MGI:2663086Mus musculusDach1tm1Mrd/Dach1tm1Mrdcyanosis, respiratory distress, neonatal lethality, complete penetrance, abnormal suckling behaviorAvailability unknown check source stock centerPMID:11238885Allele Detail: TargetedDach1tm1Mrd2663086involves: 129S7/SvEvBrd
MGIRRID:MGI:3849712Mus musculusMycbp2m274-4Tpo/Mycbp2m274-4Tpodecreased birth weight, respiratory distress, decreased birth body size, neonatal lethality, complete penetrance, hunched postureAvailability unknown check source stock centerPMID:19391113Allele Detail: Chemically induced (ENU)Mycbp2m274-4Tpo3849712involves: C57BL/6J * SSL/LeJ