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Search results 401 to 500 out of 681 for Kcnq1

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Type Details Score
Publication
19218243 | J:148806
First Author: Terrenoire C
Year: 2009
Journal: J Biol Chem
Title: The cardiac IKs potassium channel macromolecular complex includes the phosphodiesterase PDE4D3.
Volume: 284
Issue: 14
Pages: 9140-6
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Publication
10369881 | J:56342
First Author: Dao D
Year: 1999
Journal: Hum Mol Genet
Title: Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting.
Volume: 8
Issue: 7
Pages: 1337-52
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Publication
18006587 | J:176411
First Author: Sampson KJ
Year: 2008
Journal: J Physiol
Title: Adrenergic regulation of a key cardiac potassium channel can contribute to atrial fibrillation: evidence from an I Ks transgenic mouse.
Volume: 586
Issue: 2
Pages: 627-37
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Publication
10915772 | J:63702
First Author: Paulsen M
Year: 2000
Journal: Hum Mol Genet
Title: Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse.
Volume: 9
Issue: 12
Pages: 1829-41
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Publication
32127020 | J:288268
First Author: Miwa T
Year: 2020
Journal: Mol Brain
Title: Tsukushi is essential for the development of the inner ear.
Volume: 13
Issue: 1
Pages: 29
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Publication
15240882 | J:91511
First Author: Mai W
Year: 2004
Journal: Proc Natl Acad Sci U S A
Title: Thyroid hormone receptor alpha is a molecular switch of cardiac function between fetal and postnatal life.
Volume: 101
Issue: 28
Pages: 10332-7
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Publication
11007485 | J:77375
First Author: Nguyên-Trân VT
Year: 2000
Journal: Cell
Title: A novel genetic pathway for sudden cardiac death via defects in the transition between ventricular and conduction system cell lineages.
Volume: 102
Issue: 5
Pages: 671-82
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Publication
20457925 | J:160540
First Author: Wang J
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: Pitx2 prevents susceptibility to atrial arrhythmias by inhibiting left-sided pacemaker specification.
Volume: 107
Issue: 21
Pages: 9753-8
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Publication
9467008 | J:46363
First Author: Gould TD
Year: 1998
Journal: Hum Mol Genet
Title: Imprinting of mouse Kvlqt1 is developmentally regulated.
Volume: 7
Issue: 3
Pages: 483-7
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Publication
17901046 | J:132025
First Author: Labialle S
Year: 2008
Journal: Hum Mol Genet
Title: Coordinated diurnal regulation of genes from the Dlk1-Dio3 imprinted domain: implications for regulation of clusters of non-paralogous genes.
Volume: 17
Issue: 1
Pages: 15-26
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Publication
38278860 | J:344965
First Author: Udagawa T
Year: 2024
Journal: Sci Rep
Title: Loss of Pax3 causes reduction of melanocytes in the developing mouse cochlea.
Volume: 14
Issue: 1
Pages: 2210
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Publication
35372344 | J:323119
 
First Author: Renauld JM
Year: 2022
Journal: Front Cell Dev Biol
Title: Intermediate Cells of Dual Embryonic Origin Follow a Basal to Apical Gradient of Ingression Into the Lateral Wall of the Cochlea.
Volume: 10
Pages: 867153
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Publication
19136628 | J:143477
First Author: Chotalia M
Year: 2009
Journal: Genes Dev
Title: Transcription is required for establishment of germline methylation marks at imprinted genes.
Volume: 23
Issue: 1
Pages: 105-17
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Publication
9584186 | J:47668
First Author: Caspary T
Year: 1998
Journal: Mol Cell Biol
Title: Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster.
Volume: 18
Issue: 6
Pages: 3466-74
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Publication
9922400 | J:52861
First Author: Day CD
Year: 1999
Journal: Mamm Genome
Title: The imprinted domain in mouse distal Chromosome 7: reagents for mutagenesis and sequencing.
Volume: 10
Issue: 2
Pages: 182-5
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Publication
10036981 | J:52790
First Author: Ainscough JF
Year: 1998
Journal: Genet Res
Title: Mechanism of imprinting on mouse distal chromosome 7.
Volume: 72
Issue: 3
Pages: 237-45
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Publication
16141072 | J:99680
First Author: Carninci P
Year: 2005
Journal: Science
Title: The transcriptional landscape of the mammalian genome.
Volume: 309
Issue: 5740
Pages: 1559-63
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Publication
- | J:68900
     
First Author: The Jackson Laboratory Mouse Radiation Hybrid Database
Year: 2004
Journal: Database Release
Title: Mouse T31 Radiation Hybrid Data Load
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Publication
10691133 | J:66461
First Author: Kato R
Year: 1999
Journal: DNA Res
Title: Sequence-ready 1-Mb YAC, BAC and cosmid contigs covering the distal imprinted region of mouse chromosome 7.
Volume: 6
Issue: 6
Pages: 401-5
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Publication
27488639 | J:234621
First Author: Shibata S
Year: 2016
Journal: J Neurosci
Title: Hepatocyte Growth Factor-c-MET Signaling Mediates the Development of Nonsensory Structures of the Mammalian Cochlea and Hearing.
Volume: 36
Issue: 31
Pages: 8200-9
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Publication
33964205 | J:306028
First Author: Chen T
Year: 2021
Journal: Dev Cell
Title: Cochlear supporting cells require GAS2 for cytoskeletal architecture and hearing.
Volume: 56
Issue: 10
Pages: 1526-1540.e7
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Publication
37720106 | J:340735
First Author: Rose KP
Year: 2023
Journal: iScience
Title: Spatially distinct otic mesenchyme cells show molecular and functional heterogeneity patterns before hearing onset.
Volume: 26
Issue: 10
Pages: 107769
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Publication
23457544 | J:197180
First Author: Buniello A
Year: 2013
Journal: PLoS One
Title: Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness.
Volume: 8
Issue: 2
Pages: e56274
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Publication
32492036 | J:289625
First Author: Shawer H
Year: 2020
Journal: PLoS One
Title: A missense mutation of ErbB2 produces a novel mouse model of stillbirth associated with a cardiac abnormality but lacking abnormalities of placental structure.
Volume: 15
Issue: 6
Pages: e0233007
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Publication
21267068 | J:153498
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
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Publication
- | J:157972
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome U74 Array Platform (A, B, C v2).
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Publication
- | J:262123
     
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
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Publication
31570121 | J:282828
   
First Author: Fan D
Year: 2019
Journal: Elife
Title: Taste bud formation depends on taste nerves.
Volume: 8
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Publication
21925491 | J:178162
First Author: Trowe MO
Year: 2011
Journal: Dev Biol
Title: Impaired stria vascularis integrity upon loss of E-cadherin in basal cells.
Volume: 359
Issue: 1
Pages: 95-107
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Publication
18353863 | J:134489
First Author: Trowe MO
Year: 2008
Journal: Development
Title: Deafness in mice lacking the T-box transcription factor Tbx18 in otic fibrocytes.
Volume: 135
Issue: 9
Pages: 1725-34
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Publication
27287879 | J:234993
First Author: Nishiguchi Y
Year: 2016
Journal: Dev Biol
Title: Bcl11b/Ctip2 is required for development of lingual papillae in mice.
Volume: 416
Issue: 1
Pages: 98-110
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Publication
37045597 | J:335201
 
First Author: Ohmoto M
Year: 2023
Journal: eNeuro
Title: A Transcription Factor Etv1/Er81 Is Involved in the Differentiation of Sweet, Umami, and Sodium Taste Cells.
Volume: 10
Issue: 4
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Publication
33500348 | J:302583
 
First Author: Jiang W
Year: 2021
Journal: Proc Natl Acad Sci U S A
Title: ZFP57 dictates allelic expression switch of target imprinted genes.
Volume: 118
Issue: 5
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Publication
14610273 | J:86696
First Author: Zambrowicz BP
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.
Volume: 100
Issue: 24
Pages: 14109-14
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Publication
- | J:87349
     
First Author: JAX Neuroscience Mutagenesis Facility
Year: 2004
Journal: MGI Direct Data Submission
Title: Heritable mouse mutants from JAX NMF ENU Mutagenesis Program
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Publication
15163367 | J:187438
First Author: Peters J
Year: 2004
Journal: Brief Funct Genomic Proteomic
Title: Identification and characterisation of imprinted genes in the mouse.
Volume: 2
Issue: 4
Pages: 320-33
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Publication
26321200 | J:239780
First Author: Caputo L
Year: 2015
Journal: Cell Stem Cell
Title: The Isl1/Ldb1 Complex Orchestrates Genome-wide Chromatin Organization to Instruct Differentiation of Multipotent Cardiac Progenitors.
Volume: 17
Issue: 3
Pages: 287-99
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Publication
36343245 | J:332093
First Author: Szeto IYY
Year: 2022
Journal: Proc Natl Acad Sci U S A
Title: SOX9 and SOX10 control fluid homeostasis in the inner ear for hearing through independent and cooperative mechanisms.
Volume: 119
Issue: 46
Pages: e2122121119
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Publication
31550482 | J:278988
     
First Author: Tian C
Year: 2019
Journal: Dev Biol
Title: TBX1 is required for normal stria vascularis and semicircular canal development.
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Publication
22808246 | J:189624
First Author: Son EJ
Year: 2012
Journal: PLoS One
Title: Developmental gene expression profiling along the tonotopic axis of the mouse cochlea.
Volume: 7
Issue: 7
Pages: e40735
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Publication
- | J:75000
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
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Publication
31024170 | J:331853
First Author: Gao R
Year: 2019
Journal: Cell Res
Title: Pioneering function of Isl1 in the epigenetic control of cardiomyocyte cell fate.
Volume: 29
Issue: 6
Pages: 486-501
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Publication
37067297 | J:339839
First Author: Ross JA
Year: 2023
Journal: Cardiovasc Res
Title: Lem2 is essential for cardiac development by maintaining nuclear integrity.
Volume: 119
Issue: 11
Pages: 2074-2088
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Publication
26378152 | J:263568
First Author: Kim GE
Year: 2015
Journal: Cardiovasc Res
Title: LKB1 deletion causes early changes in atrial channel expression and electrophysiology prior to atrial fibrillation.
Volume: 108
Issue: 1
Pages: 197-208
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Publication
- | J:144087
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
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Publication
29107558 | J:245876
First Author: Rohacek AM
Year: 2017
Journal: Dev Cell
Title: ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development.
Volume: 43
Issue: 3
Pages: 318-331.e5
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Publication
37279265 | J:343328
First Author: Xie Z
Year: 2023
Journal: Proc Natl Acad Sci U S A
Title: ZBTB20 is essential for cochlear maturation and hearing in mice.
Volume: 120
Issue: 24
Pages: e2220867120
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Publication
- | J:141210
     
First Author: Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI)
Year: 2008
Journal: Database Download
Title: Mouse Gene Trap Data Load from dbGSS
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Publication
32212902 | J:317550
First Author: Sakamoto T
Year: 2020
Journal: Circ Res
Title: A Critical Role for Estrogen-Related Receptor Signaling in Cardiac Maturation.
Volume: 126
Issue: 12
Pages: 1685-1702
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Publication
- | J:85324
     
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
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Publication
16985003 | J:119550
First Author: Harrell MD
Year: 2007
Journal: Physiol Genomics
Title: Large-scale analysis of ion channel gene expression in the mouse heart during perinatal development.
Volume: 28
Issue: 3
Pages: 273-83
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Publication
- | J:238766
     
First Author: Shanghai Model Organisms Center
Year: 2017
Journal: MGI Direct Data Submission
Title: Information obtained from the Shanghai Model Organisms Center (SMOC), Shanghai, China
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Publication
- | J:91388
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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Publication
- | J:63103
     
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
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Publication
- | J:90438
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
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Publication
18554416 | J:139177
First Author: Hoffman BG
Year: 2008
Journal: Genome Biol
Title: Identification of transcripts with enriched expression in the developing and adult pancreas.
Volume: 9
Issue: 6
Pages: R99
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Publication
- | J:342607
       
First Author: Birgit Meldal and Sandra Orchard (1). (1) European Bioinformatics Institute (EBI), Hinxton, Cambridgeshire, United Kingdom
Year: 2023
Title: Manual transfer of experimentally-verified manual GO annotation data to homologous complexes by curator judgment of sequence, composition and function similarity
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Publication
- | J:326541
       
First Author: Cyagen Biosciences Inc.
Year: 2022
Title: Cyagen Biosciences Website.
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Publication
- | J:157065
     
First Author: Helmholtz Zentrum Muenchen GmbH
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu)
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Publication
- | J:342605
       
First Author: GOA curators
Year: 2016
Title: Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
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Publication
- | J:155856
       
First Author: The Gene Ontology Consortium
Year: 2014
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
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Publication
- | J:293217
       
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
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Publication
- | J:342587
       
First Author: AgBase, BHF-UCL, Parkinson's UK-UCL, dictyBase, HGNC, Roslin Institute, FlyBase and UniProtKB curators
Year: 2011
Title: Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
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Publication
- | J:164563
       
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
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Publication
- | J:161428
       
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
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Publication
- | J:155721
     
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
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Publication
- | J:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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Publication
- | J:53168
     
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
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Publication
- | J:144086
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
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Publication
12670483 | J:83146
First Author: Teng S
Year: 2003
Journal: Biochem Biophys Res Commun
Title: Novel gene hKCNE4 slows the activation of the KCNQ1 channel.
Volume: 303
Issue: 3
Pages: 808-13
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Publication
22721776 | J:185569
First Author: Mohammad F
Year: 2012
Journal: Development
Title: Long noncoding RNA-mediated maintenance of DNA methylation and transcriptional gene silencing.
Volume: 139
Issue: 15
Pages: 2792-803
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Publication
8900283 | -
First Author: Sanguinetti MC
Year: 1996
Journal: Nature
Title: Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.
Volume: 384
Issue: 6604
Pages: 80-3
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Publication
9020846 | -
First Author: Neyroud N
Year: 1997
Journal: Nat Genet
Title: A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.
Volume: 15
Issue: 2
Pages: 186-9
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Protein Domain
IPR005827 | K_chnl_volt-dep_KCQN1
Type: Family
Description: Potassium channels are the most diverse group of the ion channel family [, ]. They are important in shaping the action potential, and in neuronal excitability and plasticity []. The potassium channel family is composed of several functionally distinct isoforms, which can be broadly separated into 2 groups []: the practically non-inactivating 'delayed' group and the rapidly inactivating 'transient' group.These are all highly similar proteins, with only small amino acid changes causing the diversity of the voltage-dependent gating mechanism, channel conductance and toxin binding properties. Each type of K+channel is activated by different signals and conditions depending on their type of regulation: some open in response to depolarisation of the plasma membrane; others in response to hyperpolarisation or an increase in intracellular calcium concentration; some can be regulated by binding of a transmitter, together with intracellular kinases; while others are regulated by GTP-binding proteins or other second messengers []. In eukaryotic cells, K+channels are involved in neural signalling and generation of the cardiac rhythm, act as effectors in signal transduction pathways involving G protein-coupled receptors (GPCRs) and may have a role in target cell lysis by cytotoxic T-lymphocytes []. In prokaryotic cells, they play a role in the maintenance of ionic homeostasis [].All K+channels discovered so far possess a core of alpha subunits, each comprising either one or two copies of a highly conserved pore loop domain (P-domain). The P-domain contains the sequence (T/SxxTxGxG), which has been termed the K+selectivity sequence. In families that contain one P-domain, four subunits assemble to form a selective pathway for K+across the membrane. However, it remains unclear how the 2 P-domain subunits assemble to form a selective pore. The functional diversity of these families can arise through homo- or hetero-associations of alpha subunits or association with auxiliary cytoplasmic beta subunits. K+channel subunits containing one pore domain can be assigned into one of two superfamilies: those that possess six transmembrane (TM) domains and those that possess only two TM domains. The six TM domain superfamily can be further subdivided into conserved gene families: the voltage-gated (Kv) channels; the KCNQ channels (originally known as KvLQT channels); the EAG-like K+channels; and three types of calcium (Ca)-activated K+channels (BK, IK and SK) []. The 2TM domain family comprises inward-rectifying K+channels. In addition, there are K+channel alpha-subunits that possess two P-domains. These are usually highly regulated K+selective leak channels.KCNQ channels (also known as KQT-like channels) differ from other voltage-gated 6 TM helix channels, chiefly in that they possess no tetramerisation domain. Consequently, they rely on interaction with accessory subunits, or form heterotetramers with other members of the family []. Currently, 5 members of the KCNQ family are known. These have been found to be widely distributed within the body, having been shown to be expressed in the heart, brain, pancreas, lung, placenta and ear. They were initially cloned as a result of a search for proteins involved in cardiac arhythmia. Subsequently, mutations in other KCNQ family members have been shown to be responsible for some forms of hereditary deafness []and benign familial neonatal epilepsy [].KCNQ1 was the first member of the KCNQ channel family to be isolated, and has been found to be the most common cause of the disease `long QT syndrome' a cardiac arhythmia resulting in a prolonged QT interval. In exceptional cases, this can lead to sudden death, triggered by extreme stress [, ]. KCNQ1 is expressed in the stria vascularis of the inner ear, and may be the cause of hereditary deafness [].
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Publication
21084694 | J:170745
First Author: Roepke TK
Year: 2011
Journal: FASEB J
Title: Genetic dissection reveals unexpected influence of beta subunits on KCNQ1 K+ channel polarized trafficking in vivo.
Volume: 25
Issue: 2
Pages: 727-36
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Publication
11877438 | J:76523
First Author: Kanduri C
Year: 2002
Journal: J Biol Chem
Title: A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator.
Volume: 277
Issue: 20
Pages: 18106-10
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Publication
21576366 | J:174090
First Author: Jones MJ
Year: 2011
Journal: Mol Cell Biol
Title: An extended domain of Kcnq1ot1 silencing revealed by an imprinted fluorescent reporter.
Volume: 31
Issue: 14
Pages: 2827-37
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Publication
33293505 | J:306451
First Author: Yu XH
Year: 2020
Journal: Cell Death Dis
Title: LncRNA kcnq1ot1 promotes lipid accumulation and accelerates atherosclerosis via functioning as a ceRNA through the miR-452-3p/HDAC3/ABCA1 axis.
Volume: 11
Issue: 12
Pages: 1043
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Allele
Tg(Myh6-KCNQ1_i2)H05Desc | MGI:5575891
Name: transgene insertion H05, Denis Escande
Allele Type: Transgenic
Attribute String: Dominant negative, Humanized sequence, Inserted expressed sequence
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Allele
Tg(Myh6-KCNQ1_i2)H02Desc | MGI:5575890
Name: transgene insertion H02, Denis Escande
Allele Type: Transgenic
Attribute String: Dominant negative, Humanized sequence, Inserted expressed sequence
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Allele
Kcnq1ot1<+> | MGI:2439650
   
Name: KCNQ1 overlapping transcript 1; wild type
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ncRNA Gene
MGP_CAROLIEiJ_G0004094 | -
Type: ncRNA_gene
Organism: Mus caroli
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ncRNA Gene
MGP_129S1SvImJ_G0004525 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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ncRNA Gene
MGP_AJ_G0004505 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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ncRNA Gene
MGP_AKRJ_G0004488 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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ncRNA Gene
MGP_BALBcJ_G0004490 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_C3HHeJ_G0004439 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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lncRNA Gene
MGI_C57BL6J_1926855 | -
Type: lncRNA_gene
Organism: mouse, laboratory
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ncRNA Gene
MGP_C57BL6NJ_G0004640 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_CASTEiJ_G0004399 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_CBAJ_G0004434 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_DBA2J_G0004448 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_FVBNJ_G0004465 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_LPJ_G0004529 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_NODShiLtJ_G0004454 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_NZOHlLtJ_G0004639 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_PWKPhJ_G0004352 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_WSBEiJ_G0004438 | -
Type: ncRNA_gene
Organism: mouse, laboratory
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•
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ncRNA Gene
MGP_PahariEiJ_G0002227 | -
Type: ncRNA_gene
Organism: Mus pahari
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•
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ncRNA Gene
MGP_SPRETEiJ_G0004293 | -
Type: ncRNA_gene
Organism: Mus spretus
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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