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Search results 1 to 100 out of 681 for Kcnq1

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Type Details Score
Gene
3784 | KCNQ1
Type: gene
Organism: human
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Gene
450957 | KCNQ1
Type: gene
Organism: chimpanzee
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Gene
784876 | KCNQ1
Type: gene
Organism: cattle
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Gene
423090 | KCNQ1
Type: gene
Organism: chicken
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Gene
721211 | KCNQ1
Type: gene
Organism: macaque, rhesus
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Gene
100145329 | kcnq1
Type: gene
Organism: frog, western clawed
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Gene
84020 | Kcnq1
Type: gene
Organism: rat
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Gene
483669 | KCNQ1
Type: gene
Organism: dog, domestic
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Protein Coding Gene
MGI:108083 | Kcnq1
Type: protein_coding_gene
Organism: mouse, laboratory
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GXD Expression
GXD Expression
 
Probe: MGI:2060818
Assay Type: RNA in situ
Annotation Date: 2009-01-15
Strength: Strong
Sex: Not Specified
Emaps: EMAPS:3564522
Pattern: Not Specified
Stage: TS22
Assay Id: MGI:3826134
Age: embryonic day 14.5
Image: Additional file 4 Kcnq1
Specimen Label: Additional file 4 Kcnq1
Detected: true
Specimen Num: 1
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Gene
55539 | KCNQ1DN
Type: gene
Organism: human
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Publication
25539921 | J:223238
First Author: Schultz BM
Year: 2015
Journal: Nucleic Acids Res
Title: Enhancers compete with a long non-coding RNA for regulation of the Kcnq1 domain.
Volume: 43
Issue: 2
Pages: 745-59
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Gene
338653 | KCNQ1-AS1
Type: gene
Organism: human
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Publication
26100882 | J:223739
First Author: Asahara S
Year: 2015
Journal: Proc Natl Acad Sci U S A
Title: Paternal allelic mutation at the Kcnq1 locus reduces pancreatic β-cell mass by epigenetic modification of Cdkn1c.
Volume: 112
Issue: 27
Pages: 8332-7
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Publication
24395636 | J:208270
First Author: Zhang H
Year: 2014
Journal: J Cell Biol
Title: Long noncoding RNA-mediated intrachromosomal interactions promote imprinting at the Kcnq1 locus.
Volume: 204
Issue: 1
Pages: 61-75
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Publication
17021040 | J:114401
First Author: Lewis A
Year: 2006
Journal: Development
Title: Epigenetic dynamics of the Kcnq1 imprinted domain in the early embryo.
Volume: 133
Issue: 21
Pages: 4203-10
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Publication
15340049 | J:92776
First Author: Thakur N
Year: 2004
Journal: Mol Cell Biol
Title: An antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control region.
Volume: 24
Issue: 18
Pages: 7855-62
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Publication
15516932 | J:94241
First Author: Umlauf D
Year: 2004
Journal: Nat Genet
Title: Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.
Volume: 36
Issue: 12
Pages: 1296-300
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Gene
10984 | KCNQ1OT1
Type: gene
Organism: human
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Publication
23975432 | J:212747
First Author: Than BL
Year: 2014
Journal: Oncogene
Title: The role of KCNQ1 in mouse and human gastrointestinal cancers.
Volume: 33
Issue: 29
Pages: 3861-8
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Publication
17597584 | J:123033
First Author: Knollmann BC
Year: 2007
Journal: Biochem Biophys Res Commun
Title: Kcnq1 contributes to an adrenergic-sensitive steady-state K+ current in mouse heart.
Volume: 360
Issue: 1
Pages: 212-8
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Publication
19491250 | J:176794
First Author: Song P
Year: 2009
Journal: J Physiol
Title: KCNQ1 is the luminal K+ recycling channel during stimulation of gastric acid secretion.
Volume: 587
Issue: Pt 15
Pages: 3955-65
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Publication
11226272 | J:67873
First Author: Casimiro MC
Year: 2001
Journal: Proc Natl Acad Sci U S A
Title: Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome.
Volume: 98
Issue: 5
Pages: 2526-31
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Publication
20459838 | J:161410
 
First Author: Oh-McGinnis R
Year: 2010
Journal: BMC Dev Biol
Title: Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.
Volume: 10
Pages: 50
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Publication
20573698 | J:163857
First Author: Mohammad F
Year: 2010
Journal: Development
Title: Kcnq1ot1 noncoding RNA mediates transcriptional gene silencing by interacting with Dnmt1.
Volume: 137
Issue: 15
Pages: 2493-9
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Publication
26084842 | J:233544
First Author: Chang Q
Year: 2015
Journal: EMBO Mol Med
Title: Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome.
Volume: 7
Issue: 8
Pages: 1077-86
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Publication
15004216 | J:100283
First Author: Knollmann BC
Year: 2004
Journal: J Pharmacol Exp Ther
Title: Isoproterenol exacerbates a long QT phenotype in Kcnq1-deficient neonatal mice: possible roles for human-like Kcnq1 isoform 1 and slow delayed rectifier K+ current.
Volume: 310
Issue: 1
Pages: 311-8
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Publication
15327781 | J:93878
First Author: Salas M
Year: 2004
Journal: Mech Dev
Title: Placental growth retardation due to loss of imprinting of Phlda2.
Volume: 121
Issue: 10
Pages: 1199-210
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Publication
- | J:71321
     
First Author: Kim JH
Year: 2001
Journal: MGI Direct Data Submission
Title: A new spontaneous mutation in the Kcnq1 gene in mice
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Publication
- | J:112553
     
First Author: Gagnon LH
Year: 2006
Journal: MGI Direct Data Submission
Title: Vertigo-4J, a new spontaneous mouse mutation in the Kcnq1 gene
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Publication
28428215 | J:274138
First Author: Singh VB
Year: 2017
Journal: Development
Title: Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome.
Volume: 144
Issue: 10
Pages: 1820-1830
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Publication
18079696 | J:130529
First Author: Shin JY
Year: 2008
Journal: EMBO J
Title: Two distinct mechanisms of silencing by the KvDMR1 imprinting control region.
Volume: 27
Issue: 1
Pages: 168-78
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Publication
23275875 | J:218369
First Author: Fedoriw AM
Year: 2012
Journal: G3 (Bethesda)
Title: Differentiation-driven nucleolar association of the mouse imprinted Kcnq1 locus.
Volume: 2
Issue: 12
Pages: 1521-8
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Publication
17660684 | J:124275
First Author: Takagi T
Year: 2007
Journal: Exp Anim
Title: Phenotypic analysis of vertigo 2 Jackson mice with a Kcnq1 potassium channel mutation.
Volume: 56
Issue: 4
Pages: 295-300
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Publication
23542581 | J:211437
First Author: de la Rosa AJ
Year: 2013
Journal: Cardiovasc Res
Title: Functional suppression of Kcnq1 leads to early sodium channel remodelling and cardiac conduction system dysmorphogenesis.
Volume: 98
Issue: 3
Pages: 504-14
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Publication
16702402 | J:108700
First Author: Mancini-Dinardo D
Year: 2006
Journal: Genes Dev
Title: Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes.
Volume: 20
Issue: 10
Pages: 1268-82
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Publication
16896189 | J:118073
First Author: Zheng W
Year: 2007
Journal: Am J Physiol Renal Physiol
Title: Cellular distribution of the potassium channel KCNQ1 in normal mouse kidney.
Volume: 292
Issue: 1
Pages: F456-66
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Publication
20368164 | J:164618
First Author: Goldman AM
Year: 2009
Journal: Sci Transl Med
Title: Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.
Volume: 1
Issue: 2
Pages: 2ra6
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Publication
15385447 | J:94410
First Author: Elso CM
Year: 2004
Journal: Hum Mol Genet
Title: Heightened susceptibility to chronic gastritis, hyperplasia and metaplasia in Kcnq1 mutant mice.
Volume: 13
Issue: 22
Pages: 2813-21
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Publication
15891643 | J:110797
First Author: Rivas A
Year: 2005
Journal: Otol Neurotol
Title: Inner ear abnormalities in a Kcnq1 (Kvlqt1) knockout mouse: a model of Jervell and Lange-Nielsen syndrome.
Volume: 26
Issue: 3
Pages: 415-24
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Publication
23154976 | J:194689
First Author: Nguyen N
Year: 2013
Journal: Am J Physiol Gastrointest Liver Physiol
Title: Independent trafficking of the KCNQ1 K+ channel and H+-K+-ATPase in gastric parietal cells from mice.
Volume: 304
Issue: 2
Pages: G157-66
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Publication
26454161 | J:251329
First Author: Agsten M
Year: 2015
Journal: J Mol Cell Cardiol
Title: BACE1 modulates gating of KCNQ1 (Kv7.1) and cardiac delayed rectifier KCNQ1/KCNE1 (IKs).
Volume: 89
Issue: Pt B
Pages: 335-48
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Publication
21859894 | J:178399
First Author: Roepke TK
Year: 2011
Journal: FASEB J
Title: KCNE2 forms potassium channels with KCNA3 and KCNQ1 in the choroid plexus epithelium.
Volume: 25
Issue: 12
Pages: 4264-73
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Publication
12410230 | J:79882
First Author: Fitzpatrick GV
Year: 2002
Journal: Nat Genet
Title: Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1.
Volume: 32
Issue: 3
Pages: 426-31
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Publication
26241757 | J:242795
First Author: Koppes E
Year: 2015
Journal: PLoS One
Title: Partial Loss of Genomic Imprinting Reveals Important Roles for Kcnq1 and Peg10 Imprinted Domains in Placental Development.
Volume: 10
Issue: 8
Pages: e0135202
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Publication
23028363 | J:190449
First Author: Korostowski L
Year: 2012
Journal: PLoS Genet
Title: The Kcnq1ot1 long non-coding RNA affects chromatin conformation and expression of Kcnq1, but does not regulate its imprinting in the developing heart.
Volume: 8
Issue: 9
Pages: e1002956
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Publication
17245608 | J:118209
First Author: Green K
Year: 2007
Journal: Mamm Genome
Title: A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA.
Volume: 18
Issue: 1
Pages: 32-42
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Publication
19144718 | J:144190
First Author: Redrup L
Year: 2009
Journal: Development
Title: The long noncoding RNA Kcnq1ot1 organises a lineage-specific nuclear domain for epigenetic gene silencing.
Volume: 136
Issue: 4
Pages: 525-30
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Publication
16628224 | J:108785
First Author: Kanduri C
Year: 2006
Journal: EMBO J
Title: The length of the transcript encoded from the Kcnq1ot1 antisense promoter determines the degree of silencing.
Volume: 25
Issue: 10
Pages: 2096-106
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Publication
10907850 | J:63552
First Author: Yatsuki H
Year: 2000
Journal: DNA Res
Title: Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human.
Volume: 7
Issue: 3
Pages: 195-206
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Publication
15640248 | J:96366
First Author: Cerrato F
Year: 2005
Journal: Hum Mol Genet
Title: The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.
Volume: 14
Issue: 4
Pages: 503-11
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Publication
1971786 | J:10529
First Author: Bastian H
Year: 1990
Journal: EMBO J
Title: A murine even-skipped homologue, Evx 1, is expressed during early embryogenesis and neurogenesis in a biphasic manner.
Volume: 9
Issue: 6
Pages: 1839-52
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Publication
15516931 | J:94246
First Author: Lewis A
Year: 2004
Journal: Nat Genet
Title: Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.
Volume: 36
Issue: 12
Pages: 1291-5
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Publication
16314573 | J:104389
First Author: Vallon V
Year: 2005
Journal: Proc Natl Acad Sci U S A
Title: KCNQ1-dependent transport in renal and gastrointestinal epithelia.
Volume: 102
Issue: 49
Pages: 17864-9
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Publication
19369585 | J:148694
First Author: Boini KM
Year: 2009
Journal: Am J Physiol Regul Integr Comp Physiol
Title: Enhanced insulin sensitivity of gene-targeted mice lacking functional KCNQ1.
Volume: 296
Issue: 6
Pages: R1695-701
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Publication
12766260 | J:123819
First Author: Tosaka T
Year: 2003
Journal: J Pharmacol Exp Ther
Title: Nicotine induces a long QT phenotype in Kcnq1-deficient mouse hearts.
Volume: 306
Issue: 3
Pages: 980-7
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Publication
38444763 | J:345886
 
First Author: Aubin Vega M
Year: 2024
Journal: Front Physiol
Title: Function of KvLQT1 potassium channels in a mouse model of bleomycin-induced acute lung injury.
Volume: 15
Pages: 1345488
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Publication
30771304 | J:275000
First Author: Sharma A
Year: 2019
Journal: Dev Biol
Title: miR-126 regulates glycogen trophoblast proliferation and DNA methylation in the murine placenta.
Volume: 449
Issue: 1
Pages: 21-34
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Publication
31243019 | J:276955
 
First Author: Du C
Year: 2019
Journal: Biol Open
Title: Different functional roles for K+ channel subtypes in regulating small intestinal glucose and ion transport.
Volume: 8
Issue: 7
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Publication
21354127 | J:173801
First Author: Hudson QJ
Year: 2011
Journal: Dev Biol
Title: Extra-embryonic-specific imprinted expression is restricted to defined lineages in the post-implantation embryo.
Volume: 353
Issue: 2
Pages: 420-31
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Publication
11076855 | J:65742
First Author: Onyango P
Year: 2000
Journal: Genome Res
Title: Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain.
Volume: 10
Issue: 11
Pages: 1697-710
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Publication
12627233 | J:82790
First Author: Mager J
Year: 2003
Journal: Nat Genet
Title: Genome imprinting regulated by the mouse Polycomb group protein Eed.
Volume: 33
Issue: 4
Pages: 502-7
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Publication
12473685 | J:80758
First Author: Mahy NL
Year: 2002
Journal: J Cell Biol
Title: Gene density and transcription influence the localization of chromatin outside of chromosome territories detectable by FISH.
Volume: 159
Issue: 5
Pages: 753-63
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Publication
11063728 | J:65815
First Author: Engemann S
Year: 2000
Journal: Hum Mol Genet
Title: Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting.
Volume: 9
Issue: 18
Pages: 2691-706
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Publication
25331955 | J:218285
First Author: Xie R
Year: 2014
Journal: J Biol Chem
Title: Molecular mechanisms of calcium-sensing receptor-mediated calcium signaling in the modulation of epithelial ion transport and bicarbonate secretion.
Volume: 289
Issue: 50
Pages: 34642-53
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Publication
11668390 | J:72512
First Author: Choi JD
Year: 2001
Journal: Mamm Genome
Title: Microarray expression profiling of tissues from mice with uniparental duplications of chromosomes 7 and 11 to identify imprinted genes.
Volume: 12
Issue: 10
Pages: 758-64
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Publication
21233130 | J:169234
First Author: Kim JD
Year: 2011
Journal: Hum Mol Genet
Title: Rex1/Zfp42 as an epigenetic regulator for genomic imprinting.
Volume: 20
Issue: 7
Pages: 1353-62
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Publication
15498462 | J:93197
First Author: Casimiro MC
Year: 2004
Journal: Genomics
Title: Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans.
Volume: 84
Issue: 3
Pages: 555-64
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Publication
15272004 | J:93340
First Author: Dilly KW
Year: 2004
Journal: J Biol Chem
Title: Overexpression of beta2-adrenergic receptors cAMP-dependent protein kinase phosphorylates and modulates slow delayed rectifier potassium channels expressed in murine heart: evidence for receptor/channel co-localization.
Volume: 279
Issue: 39
Pages: 40778-87
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Publication
34112814 | J:322020
First Author: Lubberding AF
Year: 2021
Journal: Sci Rep
Title: Age-dependent transition from islet insulin hypersecretion to hyposecretion in mice with the long QT-syndrome loss-of-function mutation Kcnq1-A340V.
Volume: 11
Issue: 1
Pages: 12253
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Publication
26971948 | J:239349
First Author: Rannals MD
Year: 2016
Journal: Neuron
Title: Psychiatric Risk Gene Transcription Factor 4 Regulates Intrinsic Excitability of Prefrontal Neurons via Repression of SCN10a and KCNQ1.
Volume: 90
Issue: 1
Pages: 43-55
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Publication
22119056 | J:179381
First Author: Guseva N
Year: 2012
Journal: Dev Biol
Title: Antisense noncoding RNA promoter regulates the timing of de novo methylation of an imprinting control region.
Volume: 361
Issue: 2
Pages: 403-11
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Publication
11528397 | J:71531
First Author: Cleary MA
Year: 2001
Journal: Nat Genet
Title: Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice.
Volume: 29
Issue: 1
Pages: 78-82
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Publication
11223304 | J:108905
First Author: Nicolas M
Year: 2001
Journal: Hear Res
Title: KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells.
Volume: 153
Issue: 1-2
Pages: 132-45
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Publication
11889581 | J:106204
First Author: Warth R
Year: 2002
Journal: Pflugers Arch
Title: The role of KCNQ1/KCNE1 K(+) channels in intestine and pancreas: lessons from the KCNE1 knockout mouse.
Volume: 443
Issue: 5-6
Pages: 822-8
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Publication
22549510 | J:187467
First Author: Purtell K
Year: 2012
Journal: FASEB J
Title: The KCNQ1-KCNE2 K⁺ channel is required for adequate thyroid I⁻ uptake.
Volume: 26
Issue: 8
Pages: 3252-9
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Publication
20051516 | J:160721
First Author: Preston P
Year: 2010
Journal: J Biol Chem
Title: Disruption of the K+ channel beta-subunit KCNE3 reveals an important role in intestinal and tracheal Cl- transport.
Volume: 285
Issue: 10
Pages: 7165-75
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Publication
31162977 | J:289339
First Author: Zhou L
Year: 2019
Journal: FASEB J
Title: The KCNE2 potassium channel β subunit is required for normal lung function and resilience to ischemia and reperfusion injury.
Volume: 33
Issue: 9
Pages: 9762-9774
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Publication
29265344 | J:273036
First Author: Vanhoof-Villalba SL
Year: 2018
Journal: Epilepsia
Title: Pharmacogenetics of KCNQ channel activation in 2 potassium channelopathy mouse models of epilepsy.
Volume: 59
Issue: 2
Pages: 358-368
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Publication
24018950 | J:215845
First Author: Singh AK
Year: 2013
Journal: J Physiol
Title: Molecular transport machinery involved in orchestrating luminal acid-induced duodenal bicarbonate secretion in vivo.
Volume: 591
Issue: 21
Pages: 5377-91
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Publication
22219655 | J:196547
 
First Author: Liu X
Year: 2011
Journal: J Biomed Biotechnol
Title: ENU mutagenesis screen to establish motor phenotypes in wild-type mice and modifiers of a pre-existing motor phenotype in tau mutant mice.
Volume: 2011
Pages: 130947
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Publication
11527966 | J:119156
First Author: Grahammer F
Year: 2001
Journal: J Biol Chem
Title: The small conductance K+ channel, KCNQ1: expression, function, and subunit composition in murine trachea.
Volume: 276
Issue: 45
Pages: 42268-75
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Publication
26546361 | J:234526
First Author: Slaats GG
Year: 2015
Journal: J Cell Sci
Title: Screen-based identification and validation of four new ion channels as regulators of renal ciliogenesis.
Volume: 128
Issue: 24
Pages: 4550-9
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Publication
16463373 | J:174181
First Author: de Castro MP
Year: 2006
Journal: Anat Rec A Discov Mol Cell Evol Biol
Title: Protein distribution of Kcnq1, Kcnh2, and Kcne3 potassium channel subunits during mouse embryonic development.
Volume: 288
Issue: 3
Pages: 304-15
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Publication
16901941 | J:121998
First Author: Knipper M
Year: 2006
Journal: J Physiol
Title: Deafness in LIMP2-deficient mice due to early loss of the potassium channel KCNQ1/KCNE1 in marginal cells of the stria vascularis.
Volume: 576
Issue: Pt 1
Pages: 73-86
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Publication
10903843 | J:63607
First Author: Enklaar T
Year: 2000
Journal: Genomics
Title: Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene family.
Volume: 67
Issue: 2
Pages: 179-87
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Publication
24595108 | J:258659
First Author: Abbott GW
Year: 2014
Journal: Sci Signal
Title: KCNQ1, KCNE2, and Na+-coupled solute transporters form reciprocally regulating complexes that affect neuronal excitability.
Volume: 7
Issue: 315
Pages: ra22
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Publication
11557234 | J:74171
First Author: Franco D
Year: 2001
Journal: Cardiovasc Res
Title: Divergent expression of delayed rectifier K(+) channel subunits during mouse heart development.
Volume: 52
Issue: 1
Pages: 65-75
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Publication
9618174 | J:48435
First Author: Paulsen M
Year: 1998
Journal: Hum Mol Genet
Title: Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.
Volume: 7
Issue: 7
Pages: 1149-59
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Publication
11208532 | J:68046
First Author: Demolombe S
Year: 2001
Journal: Am J Physiol Cell Physiol
Title: Differential expression of KvLQT1 and its regulator IsK in mouse epithelia.
Volume: 280
Issue: 2
Pages: C359-72
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Publication
25037568 | -
First Author: Dvir M
Year: 2014
Journal: J Cell Sci
Title: Long QT mutations at the interface between KCNQ1 helix C and KCNE1 disrupt I(KS) regulation by PKA and PIP₂.
Volume: 127
Issue: Pt 18
Pages: 3943-55
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Publication
23741519 | J:200823
First Author: Li X
Year: 2013
Journal: PLoS One
Title: Endolymphatic Na⁺ and K⁺ concentrations during cochlear growth and enlargement in mice lacking Slc26a4/pendrin.
Volume: 8
Issue: 5
Pages: e65977
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Publication
29143340 | J:290594
First Author: Julio-Kalajzić F
Year: 2018
Journal: J Physiol
Title: K2P TASK-2 and KCNQ1-KCNE3 K+ channels are major players contributing to intestinal anion and fluid secretion.
Volume: 596
Issue: 3
Pages: 393-407
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ncRNA Gene
MGI:1926855 | Kcnq1ot1
Type: lncRNA_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CAROLIEiJ_G0030737 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_129S1SvImJ_G0033271 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AJ_G0033254 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AKRJ_G0033185 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_BALBcJ_G0033254 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C3HHeJ_G0032970 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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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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