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Detailed topic list for MITOMAP Web

Results from MITOMAP web retrieved at 17:21 (GMT)

HiFreqHGcalc
High Frequency Haplogroup (HFHG) Flags: Calculation Criteria For full length (FL) or control region (CR) sequences, the following conditions are applied to fla...
HumanMitoCode
The Human Mitochondrial Genetic Code Translations: ATP6, ATP8, ND1, ND2, ND3, ND4, ND4L, ND5, ND6, CO1, CO2, CO3, CytB. Phe F UUUUUC Thr T ...
HumanMitoReport
The Report of the Committee on the Human Mitochondrial Genome Adapted from the original print report: Wallace DC, Lott MT, Brown MD, Huoponen K, Torroni A 1995. R...
HumanMitoSeq
.error { color:red; background color: #FFFF00; } .rare { color:green; background color: #FFFF00; } Revised Cambridge Reference Sequence (rCRS) ...
HumanMitoSeq2Strands
.error { color:red; background color: #FFFF00; font weight:bold; } .rare { color:green; background color: #FFFF00; font weight:bold; } ...
HumanMitoStrands
Human Mitochondrial DNA H L Strands Explained The rCRS (NC_012920 ) and the original CRS (J01415.1) are sequences are described as being the "L strand". The fol...
Indels
th, td { padding: 3px; border: solid 1px #CCC; } th { text align: center; } .even { background: #EEE; } Indel Variants Converted to Comply with HG...
InsertionsSimple
MITOMAP: mtDNA Simple Insertions Last Edited: May 02, 2008 th { text align: center; } #gb footer { font size: 12px; } .mark { color: red; } #gb footer ....
InsertionsSimpleIE
MITOMAP: mtDNA Simple Insertions Last Edited: May 02, 2008 Parental Molecule Insert Size (bp) Insert (nt) Insert Point (nt) Flanking Repeats N Refe...
InsertionsSimpleTemplate
MITOMAP: mtDNA Simple Insertions Last Edited: MM:EditDate:MM Parental Molecule Insert Size (bp) Insert (nt) Insert Point (nt) Flanking Repeats N Re...
LargeDeletions
Bibliography: Large Deletions in the Human mtDNA Abnet, C. C., Huppi, K., Carrera, A., Armistead, D., McKenney, K., Hu, N., Tang, Z. Z., Taylor, P. R. and Dawsey,...
LeberDiseaseMutations
Leber's Hereditary Optic Neuropathy (LHON) Disease Mutations A. "Top 10" Primary LHON mutations, the first 3 mutations listed (in boldface) represent approximatel...
LocusATP6
The Amino Acids of mtATP6 (8527 9207) 8535 8544 8553 8562 8571 8580 5' ATG AAC GAA AAT CTG TTC GCT TCA TTC ATT GCC ...
LocusATP8
The Amino Acids of mtATP8 (8366 8572) 8374 8383 8392 8401 8410 8419 5' ATG CCC CAA CTA AAT ACT ACC GTA TGG CCC ACC ...
LocusCO1
The Amino Acids of mtCO1 (5904 7445) 5912 5921 5930 5939 5948 5957 5' ATG TTC GCC GAC CGT TGA CTA TTC TCT ACA AAC...
LocusCO2
The Amino Acids of mtCO2 (7586 8269) 7594 7603 7612 7621 7630 7639 5' ATG GCA CAT GCA GCG CAA GTA GGT CTA CAA GAC...
LocusCO3
The Amino Acids of mtCO3 (9207 9990) 9215 9224 9233 9242 9251 9260 5' ATG ACC CAC CAA TCA CAT GCC TAT CAT ATA GTA...
LocusCytB
The Amino Acids of mtCytB (14747 15887) 14755 14764 14773 14782 14791 14800 5' ATG ACC CCA ATA CGC AAA ACT AAC CCC CTA ...
LocusND1
The Amino Acids of mtND1 (3307 4262) 3315 3324 3333 3342 3351 3360 5' ATA CCC ATG GCC AAC CTC CTA CTC CTC ATT GTA C...
LocusND2
The Amino Acids of mtND2 (4470 5511) 4478 4487 4496 4505 4514 4523 5' ATT AAT CCC CTG GCC CAA CCC GTC ATC TAC TCT A...
LocusND3
The Amino Acids of mtND3 (10059 10404) 10067 10076 10085 10094 10103 10112 5' ATA AAC TTC GCC TTA ATT TTA ATA ATC AAC ACC...
LocusND4
The Amino Acids of mtND4 (10760 12137) 10768 10777 10786 10795 10804 10813 5' ATG CTA AAA CTA ATC GTC CCA ACA ATT ATA T...
LocusND4L
The Amino Acids of mtND4L (10470 10766) 10478 10487 10496 10505 10514 10523 5' ATG CCC CTC ATT TAC ATA AAT ATT ATA CTA ...
LocusND5
The Amino Acids of mtND5 (12337 14148) 12345 12354 12363 12372 12381 12390 5' ATA ACC ATG CAC ACT ACT ATA ACC ACC CTA A...
LocusND6
The Amino Acids of mtND6 (14149 14673) Reminder: mtND6 is transcribed off of the reverse strand, beginning at 14673. * N G R A I E I V I ...
MissingVariants
Patched Variants Index ID Position Refna Regna AlleleType NAChange AAChange Locus Phenotype Ethnicity 1 20100804015 896 A G polymorphism A G rRNA MT RNR1 2 201105...
MitoDiseases
MITOMAP Disease Listing / Allele Classification with links to OMIM AD: Alzheimer's Disease ADPD: Alzheimer's Disease and Parkinsons's Disease AMDF: Ataxia, Myoclo...
MitoPolypeptide
MITOMAP: Mitochondrial DNA Polypeptide Assignments Last Edited: Mar 09, 2004 th { text align: center; } #gb footer { font size: 12px; } .mark { color: re...
MitoPolypeptideIE
MITOMAP: Mitochondrial DNA Polypeptide Assignments Last Edited: Mar 09, 2004 Locus Predicted Mol. Wt. SDS PAGE MobilityTris glycine Number SDS PAGE Mobili...
MitoPolypeptideTemplate
MITOMAP: Mitochondrial DNA Polypeptide Assignments Last Edited: MM:EditDate:MM Locus Predicted Mol. Wt. SDS PAGE MobilityTris glycine Number SDS PAGE Mobi...
MitoSeqs
Complete Mitochondrial DNA Sequences The revised Cambridge Reference Sequence (rCRS) is GenBank number NC_012920. Please use this new number when citing the rCRS ...
MitoSeqsBak
Complete Mitochondrial DNA Sequences The revised Cambridge Reference Sequence (rCRS) is GenBank number NC_012920. Please use this new number when citing the rCRS ...
MitoSites
MitoSites Mitochondrial Resources on the Web C. elegans Mitochondrial Directory (UK) Complex I Database (Scripps) DNA Polymerase Gamma Mutation Database EMPOP Co...
MitoTipInfo
MitoTIP An in silico tool for predicting pathogenicity of novel mitochondrial tRNA variants, developed by Neal Sondheimer and Sanjay Sonney (http://journals.plos....
MitoTipScores
th, .range { text align: center; } th, td { padding left: 20px; padding right: 20px; } MitoTip Scores The current MitoTip scores are available for downloadi...
Mitobank
MITOBANKMitochondrial DNA Sequences To submit unpublished mtDNA variant data to an online database, please contact lishen #64;chla.usc.edu at MSeqDR. To submit se...
MitobankCounts1
61,134 (FL)81,124 (CR) as of 2024 01 16
MitobankCounts2
67,306 (FL)81,777 (CR) as of 2024 11 30
MitomapFigures
MITOMAP Figures The following figures require Adobe Acrobat Reader. Click here to download. Figure 1: Mitochondrial DNA Map Figure 2: Eleven pathological mutat...
MoleDay
October 23rd is being celebrated as "*Mole Day*" by chemists. A mole is a group of atoms or molecules which number 6.02 times 10 to the 23rd power. For any chemi...
MutationsCodingControl
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: Coding and Control Region Point Mutations Last Edited: Nov 20, 2024 The GB frequency data in Mitom...
MutationsCodingControlCfrm
MITOMAP: Mitochondrial DNA Base Substitution Diseases:Coding and Control Region Point Mutations with Cfrm Status Last Edited: Nov 20, 2024 For Mitomap to assign a...
MutationsCodingControlCfrmIE
MITOMAP: Mitochondrial DNA Base Substitution Diseases:Coding and Control Region Point Mutations with Cfrm Status Last Edited: Nov 20, 2024 For Mitomap to assign a...
MutationsCodingControlCfrmTemplate
MITOMAP: Mitochondrial DNA Base Substitution Diseases:Coding and Control Region Point Mutations with Cfrm Status Last Edited: MM:EditDate:MM For Mitomap to assign...
MutationsCodingControlIE
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: Coding and Control Region Point Mutations Last Edited: Nov 20, 2024 The GB frequency data in Mitom...
MutationsCodingControlTemplate
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: Coding and Control Region Point Mutations Last Edited: MM:EditDate:MM The GB frequency data in Mit...
MutationsLHON
DIV.Section1 { page: Section1 } Leber's Hereditary Optic Neuropathy (LHON) Disease Mutations A. "Top 19" Primary LHON mutations, the first 3 mutations listed...
MutationsRNA
MITOMAP: Reported Mitochondrial DNA Base Substitution Diseases: rRNA/tRNA mutations Last Edited: Nov 14, 2024 The GB frequency data in Mitomap is derived from 61...
MutationsRNACfrm
MITOMAP: Mitochondrial DNA Base Substitution Diseases:rRNA/tRNA Mutations with Cfrm Status Last Edited: Nov 14, 2024 For Mitomap to assign a status of "Cfrm" to a...
MutationsRNACfrmIE
MITOMAP: Mitochondrial DNA Base Substitution Diseases:rRNA/tRNA Mutations with Crfm Status Last Edited: Nov 14, 2024 For Mitomap to assign a status of "Cfrm" to ...
Number of topics: 50
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Topic revision: r1 - 15 Sep 2015, UnknownUser

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