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Search results 101 to 200 out of 231 for Fanci

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Hits by Pathway

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Hits by Category

Type Details Score
Protein
B2RSU4
Organism: Mus musculus/domesticus
Length: 1450  
Fragment?: false
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Protein
Q3U202
Organism: Mus musculus/domesticus
Length: 1429  
Fragment?: true
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Protein
Q3TLN3
Organism: Mus musculus/domesticus
Length: 1144  
Fragment?: true
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Protein
A0A0N4SV29
Organism: Mus musculus/domesticus
Length: 1437  
Fragment?: false
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Protein
A0A0N4SVS0
Organism: Mus musculus/domesticus
Length: 84  
Fragment?: true
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Protein
Q3UQJ0
Organism: Mus musculus/domesticus
Length: 1450  
Fragment?: false
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Publication
23444773 | -
First Author: Yao CJ
Year: 2013
Journal: Pharmazie
Title: Fanconi anemia pathway--the way of DNA interstrand cross-link repair.
Volume: 68
Issue: 1
Pages: 5-11
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Publication
11530803 | -
First Author: Yamashita T
Year: 2001
Journal: Int J Hematol
Title: Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes.
Volume: 74
Issue: 1
Pages: 33-41
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Publication
20603073 | -
First Author: Smogorzewska A
Year: 2010
Journal: Mol Cell
Title: A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair.
Volume: 39
Issue: 1
Pages: 36-47
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Publication
20603016 | -
First Author: Kratz K
Year: 2010
Journal: Cell
Title: Deficiency of FANCD2-associated nuclease KIAA1018/FAN1 sensitizes cells to interstrand crosslinking agents.
Volume: 142
Issue: 1
Pages: 77-88
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Publication
20603015 | -
First Author: MacKay C
Year: 2010
Journal: Cell
Title: Identification of KIAA1018/FAN1, a DNA repair nuclease recruited to DNA damage by monoubiquitinated FANCD2.
Volume: 142
Issue: 1
Pages: 65-76
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Publication
21464321 | -
First Author: Yamamoto KN
Year: 2011
Journal: Proc Natl Acad Sci U S A
Title: Involvement of SLX4 in interstrand cross-link repair is regulated by the Fanconi anemia pathway.
Volume: 108
Issue: 16
Pages: 6492-6
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Publication
24556218 | -
First Author: Yeo JE
Year: 2014
Journal: Hum Mol Genet
Title: CtIP mediates replication fork recovery in a FANCD2-regulated manner.
Volume: 23
Issue: 14
Pages: 3695-705
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Protein Domain
IPR029448 | FANCD2
Type: Family
Description: The Fanconi Anemia (FA) pathway is responsible for interstrand crosslink DNA repair []. The name originates the recessive syndrome known as Fanconi anemia, which causes developmental problems and cancer predisposition []. In this pathway, the FANCI-FANCD2 (ID) complex is ubiquitinated by the FA core complex and then travels to sites of damage to coordinate repair [, ]. FA pathway activation seems to trigger dissociation of FANCD2 from FANCI, coinciding with FANCD2 monoubiquitination which precedes monoubiquitination of FANCI []. This suggests a functional separation for FANCD2 from FANCI [].Monoubiquitinated FANCD2 functions to recruit DNA repair factors FAN1 (Fanconi-associated nuclease 1) []and SLX4 [], suggesting that chromatin-bound FANCD2Ub is a docking platform for certain DNA repair nucleases. FANCD2 has also a role in replication fork recovery [].
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Protein
P50652
Organism: Mus musculus/domesticus
Length: 591  
Fragment?: false
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Protein
Q3UI88
Organism: Mus musculus/domesticus
Length: 660  
Fragment?: true
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Protein
A0A1D5RLC1
Organism: Mus musculus/domesticus
Length: 169  
Fragment?: true
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Protein
E0CYQ7
Organism: Mus musculus/domesticus
Length: 229  
Fragment?: true
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Protein
A0A1Y7VKS5
Organism: Mus musculus/domesticus
Length: 412  
Fragment?: false
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Protein
E0CXC4
Organism: Mus musculus/domesticus
Length: 212  
Fragment?: true
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Protein
E0CYI2
Organism: Mus musculus/domesticus
Length: 43  
Fragment?: true
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Protein
E9QAE8
Organism: Mus musculus/domesticus
Length: 461  
Fragment?: false
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Protein
F7DEE2
Organism: Mus musculus/domesticus
Length: 117  
Fragment?: true
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Protein
E0CYC3
Organism: Mus musculus/domesticus
Length: 216  
Fragment?: true
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Protein
Q3V2X6
Organism: Mus musculus/domesticus
Length: 283  
Fragment?: false
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Protein
Q8CBR3
Organism: Mus musculus/domesticus
Length: 558  
Fragment?: false
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Protein Domain
IPR000686 | FANCC
Type: Family
Description: Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages. The FA complex repairs the interstrand cross-linking (ICL) lesions and coordinates activities of the downstream DNA repair pathway including nucleotide excision repair, translesion synthesis, and homologous recombination. It is required for the monoubiquitylation of FANCD2 and FANCI heterodimer. The FA core complex consists of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM, FANCT (UBET2), FAAP100 and FAAP24 [, ].This entry represents FANCC [].
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Protein Domain
IPR003516 | FANCA
Type: Family
Description: Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages. The FA complex repairs the interstrand cross-linking (ICL) lesions and coordinates activities of the downstream DNA repair pathway including nucleotide excision repair, translesion synthesis, and homologous recombination. It is required for the monoubiquitylation of FANCD2 and FANCI heterodimer. The FA core complex consists of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM, FANCT (UBET2), FAAP100 and FAAP24 [, ].This entry represents FANCA [].
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Protein
Q80X51
Organism: Mus musculus/domesticus
Length: 258  
Fragment?: false
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Publication
18212739 | -
First Author: Wilson JB
Year: 2008
Journal: Oncogene
Title: FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3.
Volume: 27
Issue: 26
Pages: 3641-52
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Protein Domain
IPR031729 | Fanconi_A_N
Type: Domain
Description: Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages. The FA complex repairs the interstrand cross-linking (ICL) lesions and coordinates activities of the downstream DNA repair pathway including nucleotide excision repair, translesion synthesis, and homologous recombination. It is required for the monoubiquitylation of FANCD2 and FANCI heterodimer. The FA core complex consists of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM, FANCT (UBET2), FAAP100 and FAAP24 [, ].This entry represents the N-terminal domain of FANCA.
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Protein Domain
IPR039684 | FANCG
Type: Family
Description: Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages. This entry represents FANCG, which is part of the FA core complex required for the monoubiquitylation of FANCD2 and the FANCI heterodimer. The FA complex coordinates activities of the downstream DNA repair pathway including nucleotide excision repair, translesion synthesis, and homologous recombination []. Besides being part of the FA complex, FANCG also promotes formation of a protein complex containing BRCA2, FANCD2 and XRCC3 [].
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Protein Domain
IPR039685 | FANCE
Type: Family
Description: Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages. The FA complex repairs the interstrand cross-linking (ICL) lesions and coordinates activities of the downstream DNA repair pathway including nucleotide excision repair, translesion synthesis, and homologous recombination. It is required for the monoubiquitylation of FANCD2 and FANCI heterodimer. The FA core complex consists of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM, FANCT (UBET2), FAAP100 and FAAP24 [, ].The FA group E protein (FANCE) has an important role in DNA repair, functioning as the FANCD2-binding protein in the FA core complex [].
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Publication
22012619 | J:177489
First Author: Blazek D
Year: 2011
Journal: Genes Dev
Title: The Cyclin K/Cdk12 complex maintains genomic stability via regulation of expression of DNA damage response genes.
Volume: 25
Issue: 20
Pages: 2158-72
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Protein
Q9JL70
Organism: Mus musculus/domesticus
Length: 1439  
Fragment?: false
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Protein
B2RWU3
Organism: Mus musculus/domesticus
Length: 1439  
Fragment?: false
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Protein
D3Z6Y5
Organism: Mus musculus/domesticus
Length: 481  
Fragment?: false
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Protein
F7CAP1
Organism: Mus musculus/domesticus
Length: 246  
Fragment?: true
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Protein
F7CK17
Organism: Mus musculus/domesticus
Length: 771  
Fragment?: true
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Publication
29017571 | -
First Author: Bhattacharjee S
Year: 2017
Journal: Cell Commun Signal
Title: DNA damage response and cancer therapeutics through the lens of the Fanconi Anemia DNA repair pathway.
Volume: 15
Issue: 1
Pages: 41
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Publication
22036606 | J:330492
First Author: van de Vrugt HJ
Year: 2011
Journal: DNA Repair (Amst)
Title: Evidence for complete epistasis of null mutations in murine Fanconi anemia genes Fanca and Fancg.
Volume: 10
Issue: 12
Pages: 1252-61
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Protein
A2ACJ2
Organism: Mus musculus/domesticus
Length: 879  
Fragment?: false
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Protein
Q9D7M0
Organism: Mus musculus/domesticus
Length: 421  
Fragment?: false
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Publication
17938197 | -
First Author: Alpi A
Year: 2007
Journal: Mol Cell Biol
Title: UBE2T, the Fanconi anemia core complex, and FANCD2 are recruited independently to chromatin: a basis for the regulation of FANCD2 monoubiquitination.
Volume: 27
Issue: 24
Pages: 8421-30
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Publication
12973351 | J:86047
First Author: Meetei AR
Year: 2003
Journal: Nat Genet
Title: A novel ubiquitin ligase is deficient in Fanconi anemia.
Volume: 35
Issue: 2
Pages: 165-70
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Publication
15502827 | -
First Author: Meetei AR
Year: 2004
Journal: Nat Genet
Title: X-linked inheritance of Fanconi anemia complementation group B.
Volume: 36
Issue: 11
Pages: 1219-24
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Publication
22287633 | -
First Author: Sato K
Year: 2012
Journal: Nucleic Acids Res
Title: DNA robustly stimulates FANCD2 monoubiquitylation in the complex with FANCI.
Volume: 40
Issue: 10
Pages: 4553-61
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Publication
17396147 | -
First Author: Ling C
Year: 2007
Journal: EMBO J
Title: FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway.
Volume: 26
Issue: 8
Pages: 2104-14
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Publication
16633336 | -
First Author: Huang TT
Year: 2006
Journal: Nat Rev Mol Cell Biol
Title: Regulation of DNA repair by ubiquitylation.
Volume: 7
Issue: 5
Pages: 323-34
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Publication
16531995 | -
First Author: Huang TT
Year: 2006
Journal: Nat Cell Biol
Title: Regulation of monoubiquitinated PCNA by DUB autocleavage.
Volume: 8
Issue: 4
Pages: 339-47
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Publication
15694335 | -
First Author: Nijman SM
Year: 2005
Journal: Mol Cell
Title: The deubiquitinating enzyme USP1 regulates the Fanconi anemia pathway.
Volume: 17
Issue: 3
Pages: 331-9
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Publication
19686080 | -
 
First Author: Moldovan GL
Year: 2009
Journal: Annu Rev Genet
Title: How the fanconi anemia pathway guards the genome.
Volume: 43
Pages: 223-49
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Protein Domain
IPR026985 | FAAP24
Type: Family
Description: Fanconi anemia-associated protein of 24kDa (FAAP24) plays a role in DNA repair through recruitment of the FA core complex to damaged DNA. It regulates FANCD2 monoubiquitination upon DNA damage. When repressed, it induces chromosomal instability as well as hypersensitivity to DNA cross-linking agents. It targets FANCM/FAAP24 complex to the DNA, preferentially to single strand DNA [].Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages. The FA complex repairs the interstrand cross-linking (ICL) lesions and coordinates activities of the downstream DNA repair pathway including nucleotide excision repair, translesion synthesis, and homologous recombination. It is required for the monoubiquitylation of FANCD2 and FANCI heterodimer. The FA core complex consists of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM, FANCT (UBET2), FAAP100 and FAAP24 [, ].
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Protein Domain
IPR026848 | Fancl
Type: Family
Description: Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages. The FA complex repairs the interstrand cross-linking (ICL) lesions and coordinates activities of the downstream DNA repair pathway including nucleotide excision repair, translesion synthesis, and homologous recombination. It is required for the monoubiquitylation of FANCD2 and FANCI heterodimer. The FA core complex consists of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM, FANCT (UBET2), FAAP100 and FAAP24 [, ].FANCL is an ubiquitin ligase that mediates monoubiquitination of FANCD2, a key step in the repair of interstrand DNA crosslinks (ICLs) in the Fanconi anemia (FA) pathway [, ]. In humans, defects in FANCL are the cause of Fanconi anemia complementation group L (FANCL). FANCL is a disorder affecting all bone marrow elements and resulting in anemia, leukopenia and thrombopenia. At the cellular level it is associated with hypersensitivity to DNA-damaging agents, chromosomal instability (increased chromosome breakage) and defective DNA repair [, ].
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Protein Domain
IPR029251 | Faap100
Type: Family
Description: Fanconi anemia-associated protein of 100kDa (FAAP100) is component of the Fanconi anemia (FA) core complex, which plays a central role in FA-associated DNA damage response. FAAP100 is essential for the stability and function of the complex [].Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages. The FA complex repairs the interstrand cross-linking (ICL) lesions and coordinates activities of the downstream DNA repair pathway including nucleotide excision repair, translesion synthesis, and homologous recombination. It is required for the monoubiquitylation of FANCD2 and FANCI heterodimer. The FA core complex consists of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM, FANCT (UBET2), FAAP100 and FAAP24 [, ].
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Protein Domain
IPR033815 | USP1
Type: Domain
Description: Peptidase C19 contains ubiquitin hydrolases. They are intracellular peptidases that remove ubiquitin molecules from polyubiquitinated peptides by cleavage of isopeptide bonds. They hydrolyze bonds involving the carboxyl group of the C-terminal Gly residue of ubiquitin. The purpose of the de-ubiquitination is thought to be editing of the ubiquitin conjugates, which could rescue them from degradation, as well as recycling of the ubiquitin. The ubiquitin/proteasome system is responsible for most protein turnover in the mammalian cell, and with over 50 members, family C19 is one of the largest families of peptidases in the human genome [, ].This entry encompasses ubiquitin-specific hydrolase 1 (MEROPS identifier C19.019). It is required for deubiquitination of monoubiquitinated proteins involved in various DNA repair pathways and is a key regulator of DNA repair mechanisms []. Substrates include monoubiquitinated PCNA [], and components FANCD2 []and FANCI []of the Fanconi anemia pathway, a genetic disorder that resultsin the inability to monoubiquitinate these components [].
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Protein Domain
IPR035428 | FANCF
Type: Family
Description: Fanconi anemia (FA) is a human disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages. The FA complex repairs the interstrand cross-linking (ICL) lesions and coordinates activities of the downstream DNA repair pathway including nucleotide excision repair, translesion synthesis, and homologous recombination. It is required for the monoubiquitylation of FANCD2 and FANCI heterodimer. The FA core complex consists of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM, FANCT (UBET2), FAAP100 and FAAP24 [, ].Fanconi anemia group F protein (FANCF) is a component of the FA core complex [, ]. FANCF regulates its own expression by methylation at both mRNA and protein levels. Methylation-induced inactivation of FANCF has an important role on the occurrence of ovarian cancers by disrupting the FA-BRCA pathway [].This entry also includes homologues from plants.
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Protein Coding Gene
MGI:3045266 | Fan1
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CAROLIEiJ_G0029827 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_129S1SvImJ_G0032336 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AJ_G0032315 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AKRJ_G0032251 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_BALBcJ_G0032327 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C3HHeJ_G0032040 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGI_C57BL6J_3045266 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C57BL6NJ_G0032820 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CASTEiJ_G0031369 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CBAJ_G0032006 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_DBA2J_G0032162 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_FVBNJ_G0032116 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_LPJ_G0032242 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NODShiLtJ_G0032153 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NZOHlLtJ_G0032837 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PWKPhJ_G0031089 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_WSBEiJ_G0031487 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PahariEiJ_G0013052 | -
Type: protein_coding_gene
Organism: Mus pahari
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Protein Coding Gene
MGP_SPRETEiJ_G0030930 | -
Type: protein_coding_gene
Organism: Mus spretus
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Publication
24981866 | J:217316
First Author: Pennell S
Year: 2014
Journal: Cell Rep
Title: FAN1 activity on asymmetric repair intermediates is mediated by an atypical monomeric virus-type replication-repair nuclease domain.
Volume: 8
Issue: 1
Pages: 84-93
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Publication
27026368 | J:242198
First Author: Airik R
Year: 2016
Journal: J Am Soc Nephrol
Title: A FANCD2/FANCI-Associated Nuclease 1-Knockout Model Develops Karyomegalic Interstitial Nephritis.
Volume: 27
Issue: 12
Pages: 3552-3559
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GXD Expression
GXD Expression
 
Assay Type: In situ reporter (knock in)
Annotation Date: 2021-04-16
Strength: Present
Sex: Male
Emaps: EMAPS:1868128
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6692889
Age: postnatal adult
Image: UC Davis_1859386
Note: vas deferens
Specimen Label: UC Davis_1859386
Detected: true
Specimen Num: 4
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GXD Expression
GXD Expression
   
Assay Type: In situ reporter (knock in)
Annotation Date: 2021-04-16
Strength: Present
Sex: Male
Emaps: EMAPS:1797228
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6692889
Age: postnatal adult
Image: UC Davis_1859383
Specimen Label: UC Davis_1859383
Detected: true
Specimen Num: 1
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GXD Expression
GXD Expression
   
Assay Type: In situ reporter (knock in)
Annotation Date: 2021-04-16
Strength: Present
Sex: Male
Emaps: EMAPS:1797228
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6692889
Age: postnatal adult
Image: UC Davis_1859384
Specimen Label: UC Davis_1859384
Detected: true
Specimen Num: 2
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GXD Expression
GXD Expression
   
Assay Type: In situ reporter (knock in)
Annotation Date: 2021-04-16
Strength: Present
Sex: Male
Emaps: EMAPS:1929028
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6692889
Age: postnatal adult
Image: UC Davis_1859385
Specimen Label: UC Davis_1859385
Detected: true
Specimen Num: 3
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Publication
20347428 | -
First Author: Yan Z
Year: 2010
Journal: Mol Cell
Title: A histone-fold complex and FANCM form a conserved DNA-remodeling complex to maintain genome stability.
Volume: 37
Issue: 6
Pages: 865-78
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Protein
B8JJD8
Organism: Mus musculus/domesticus
Length: 384  
Fragment?: false
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Protein
B8JJD5
Organism: Mus musculus/domesticus
Length: 462  
Fragment?: false
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Protein
B8JJD2
Organism: Mus musculus/domesticus
Length: 71  
Fragment?: true
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Protein
F7DAL6
Organism: Mus musculus/domesticus
Length: 484  
Fragment?: false
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Protein
B8JJD1
Organism: Mus musculus/domesticus
Length: 151  
Fragment?: true
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Protein
B8JJD6
Organism: Mus musculus/domesticus
Length: 406  
Fragment?: false
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Protein
Q3UY28
Organism: Mus musculus/domesticus
Length: 412  
Fragment?: true
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Protein
B8JJD3
Organism: Mus musculus/domesticus
Length: 526  
Fragment?: false
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Protein
A0A3B2W3J1
Organism: Mus musculus/domesticus
Length: 355  
Fragment?: true
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•
•
•
•
Protein
B8JJD7
Organism: Mus musculus/domesticus
Length: 154  
Fragment?: true
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•
•
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•
Protein
Q8R3Z2
Organism: Mus musculus/domesticus
Length: 171  
Fragment?: false
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•
•
•
•
Publication
17308347 | -
First Author: Nookala RK
Year: 2007
Journal: Nucleic Acids Res
Title: Insights into Fanconi Anaemia from the structure of human FANCE.
Volume: 35
Issue: 5
Pages: 1638-48
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Protein
E9Q5Z5
Organism: Mus musculus/domesticus
Length: 343  
Fragment?: false
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Publication
17289582 | J:320165
First Author: Ciccia A
Year: 2007
Journal: Mol Cell
Title: Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.
Volume: 25
Issue: 3
Pages: 331-43
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Publication
17768402 | -
First Author: Wang W
Year: 2007
Journal: Nat Rev Genet
Title: Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins.
Volume: 8
Issue: 10
Pages: 735-48
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Publication
16418574 | -
First Author: Wang Z
Year: 2006
Journal: Cancer Biol Ther
Title: Promoter hypermethylation of FANCF plays an important role in the occurrence of ovarian cancer through disrupting Fanconi anemia-BRCA pathway.
Volume: 5
Issue: 3
Pages: 256-60
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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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