C57BL/6NTac-Hiratm1a(EUCOMM)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:05901 |
International strain name | C57BL/6NTac-Hiratm1a(EUCOMM)Wtsi/WtsiIeg |
Alternative name | EPD0181_1_A05 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Hiratm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Hira |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0181_1_A05. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References |
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Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- decreased leukocyte cell number / MGI
- abnormal heart morphology / MGI
- abnormal heart development / MGI
- abnormal heart tube morphology / MGI
- abnormal head morphology / MGI
- abnormal forebrain morphology / MGI
- abnormal brain development / MGI
- open neural tube / MGI
- abnormal blood vessel morphology / MGI
- irregular heartbeat / MGI
- abnormal embryo development / MGI
- abnormal axial mesoderm / MGI
- incomplete somite formation / MGI
- abnormal somite shape / MGI
- failure to gastrulate / MGI
- decreased embryo size / MGI
- abnormal embryo turning / MGI
- abnormal left-right axis patterning / MGI
- abnormal allantois morphology / MGI
- embryonic growth arrest / MGI
- pericardial edema / MGI
- abnormal developmental patterning / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal neural tube morphology / MGI
- abnormal primitive streak morphology / MGI
- abnormal notochord morphology / MGI
- abnormal pharyngeal arch morphology / MGI
- no phenotypic analysis / MGI
- abnormal vitelline vasculature morphology / MGI
- decreased rib number / MGI
- kinked neural tube / MGI
- embryonic growth retardation / MGI
- caudal body truncation / MGI
- abnormal midbrain-hindbrain boundary development / MGI
- failure of heart looping / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- abnormal prechordal plate morphology / MGI
- enlarged allantois / MGI
- abnormal rostral-caudal axis patterning / MGI
- embryo phenotype / MGI
- abnormal neural plate morphology / MGI
- abnormal hindbrain development / MGI
- abnormal paraxial mesoderm morphology / MGI
- abnormal mesendoderm development / MGI
- failure of chorioallantoic fusion / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal head mesenchyme morphology / MGI
- decreased somite size / MGI
- embryonic-extraembryonic boundary constriction / MGI
Literature references
- Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.;White Jacqueline K, Gerdin Anna-Karin, Karp Natasha A, Ryder Ed, Buljan Marija, Bussell James N, Salisbury Jennifer, Clare Simon, Ingham Neil J, Podrini Christine, Houghton Richard, Estabel Jeanne, Bottomley Joanna R, Melvin David G, Sunter David, Adams Niels C, null null, Tannahill David, Logan Darren W, Macarthur Daniel G, Flint Jonathan, Mahajan Vinit B, Tsang Stephen H, Smyth Ian, Watt Fiona M, Skarnes William C, Dougan Gordon, Adams David J, Ramirez-Solis Ramiro, Bradley Allan, Steel Karen P, ;2013;Cell;154;452-64; 23870131
- The histone H3.3 chaperone HIRA restrains erythroid-biased differentiation of adult hematopoietic stem cells.;Murdaugh Rebecca L, Hoegenauer Kevin A, Kitano Ayumi, Holt Matthew V, Hill Matthew C, Shi Xiangguo, Tiessen Jonathan F, Chapple Richard, Hu Tianyuan, Tseng Yu-Jung, Lin Angelique, Martin James F, Young Nicolas L, Nakada Daisuke, ;2021;Stem cell reports;16;2014-2028; 34242617
- Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth.;Jeanne Médéric, Vuillaume Marie-Laure, Ung Dévina C, Vancollie Valerie E, Wagner Christel, Collins Stephan C, Vonwill Sandrine, Haye Damien, Chelloug Nora, Pfundt Rolph, Kummeling Joost, Moizard Marie-Pierre, Marouillat Sylviane, Kleefstra Tjitske, Yalcin Binnaz, Laumonnier Frédéric, Toutain Annick, ;2021;Human genetics;140;885-896; 33417013
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