about
P688
Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cellsThe XRCC2 and XRCC3 repair genes are required for chromosome stability in mammalian cellsDifferential contributions of mammalian Rad54 paralogs to recombination, DNA damage repair, and meiosisPARP1-dependent recruitment of KDM4D histone demethylase to DNA damage sites promotes double-strand break repairFBH1 helicase disrupts RAD51 filaments in vitro and modulates homologous recombination in mammalian cellsMutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female miceBRCA2 acts as a RAD51 loader to facilitate telomere replication and cappingRAD51 mutants cause replication defects and chromosomal instabilityEpithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout miceTargeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasiaAnalysis of murine Brca2 reveals conservation of protein-protein interactions but differences in nuclear localization signalsEmbryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2Genetic steps of mammalian homologous repair with distinct mutagenic consequencesMouse maelstrom, a component of nuage, is essential for spermatogenesis and transposon repression in meiosisThe cohesin subunit RAD21L functions in meiotic synapsis and exhibits sexual dimorphism in fertilityRole for the mammalian Swi5-Sfr1 complex in DNA strand break repair through homologous recombinationRad51 expression and localization in B cells carrying out class switch recombinationMouse TEX15 is essential for DNA double-strand break repair and chromosomal synapsis during male meiosisMouse HFM1/Mer3 is required for crossover formation and complete synapsis of homologous chromosomes during meiosisPositional cloning and characterization of Mei1, a vertebrate-specific gene required for normal meiotic chromosome synapsis in miceFancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in miceInfertility and aneuploidy in mice lacking a type IA DNA topoisomerase III betaFunctional conservation of Mei4 for meiotic DNA double-strand break formation from yeasts to miceDSS1 is required for RAD51 focus formation and genomic stability in mammalian cellsDisruption of CHTF18 causes defective meiotic recombination in male miceMammalian CNTD1 is critical for meiotic crossover maturation and deselection of excess precrossover sitesThe Mre11 complex influences DNA repair, synapsis, and crossing over in murine meiosisMeiotic arrest and aneuploidy in MLH3-deficient miceHORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytesAlignment of Homologous Chromosomes and Effective Repair of Programmed DNA Double-Strand Breaks during Mouse Meiosis Require the Minichromosome Maintenance Domain Containing 2 (MCMDC2) Protein
P921
Q22003975-0471F32B-A6A1-4305-852F-C42D699DBD47Q22010434-9E44330B-687E-4DC6-8FB2-5E222C16DE07Q24301697-E1B7AFF6-03F7-4730-AE70-312101C7083CQ24337719-50A9AEB4-3E4F-401F-A476-36690671C7E0Q24338079-CABF580A-F82B-485C-8079-E3C425D701CFQ24606421-E76D55F0-CC54-4339-87F2-0B2B9ECBE0D4Q28115349-91D69487-90B6-4951-855F-8112B511F1E7Q28115721-CD35545A-C77B-4D04-BED5-17AA2743A811Q28191400-963116D4-8ED8-45DF-8A82-A335742B1710Q28201015-445C0E25-AADA-43E0-9A89-55662D2BD7F8Q28209536-3309ADCE-E2C7-497E-934B-71BDFD133C4DQ28236543-5F3183D1-BD7F-4914-A4FD-3F4C56627077Q28287955-07A18625-E39D-43A5-AA3E-346957649438Q28504811-2C2B16EF-0911-4B97-9B94-51969F505EA7Q28507130-A1AC8CD7-D0EC-4AFB-BFDE-A3AF97114E52Q28508150-FE024F06-956E-401E-8775-DF11171555D6Q28508346-62374563-DD04-4B7F-B6B0-48C55B41700DQ28512197-55AF6569-DC16-4360-BA89-B066940F0FC9Q28512386-95E696D7-1C54-4219-8FF4-828A862D9EB2Q28512598-4463BA2E-0E39-42A6-8BE1-E02B55D8E763Q28513158-6A7DA006-4E32-42EA-99B3-74ACD0C3C6FAQ28586376-A20FFEE3-5185-4AF7-9CE9-37DCECA2EF53Q28586489-84FC13B8-A371-45F2-828E-C96A3D1D3E37Q28586983-562B1CE6-6EA7-48B2-96EF-65577D887910Q28587256-CEBD3968-28E5-484B-B830-B720CC9CBCEFQ28592214-E19DDA41-A569-4B1E-A790-F72C2812395CQ28592328-BF3EC6C6-9B1D-42CC-A7D2-48E4ECD56BF1Q28593875-9D1D08BA-E0BC-4E64-BCB9-680376522891Q28594947-E926E23B-21FF-404B-8B8A-442CB64AAAC7Q28771502-05306127-C181-4899-80DC-D1696B10E9DF
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in RAD51 recombinase
@nl
protèin
@ace
protéine
@fr
بروتين في فأر المنازل
@ar
name
RAD51 recombinase
@en
type
label
RAD51 recombinase
@en
altLabel
DNA repair protein RAD51 homolog 1
@en
RAD51 homolog A
@en
Rad51
@en
prefLabel
RAD51 recombinase
@en
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ENSMUSP00000028795
ENSMUSP00000117939
ENSMUSP00000119101
ENSMUSP00000119444