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FTMT Gene

protein-coding   GIFtS: 52
GCID: GC05P121187

Ferritin Mitochondrial

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(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
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Aliases
Ferritin Mitochondrial1 2
EC 1.16.3.13 8
MTF2
Ferritin H Subunit2
Ferritin, Mitochondrial2
Mitochondrial Ferritin2

External Ids:    HGNC: 173451   Entrez Gene: 940332   Ensembl: ENSG000001818677   OMIM: 6088475   UniProtKB: Q8N4E73   

Export aliases for FTMT gene to outside databases

Previous GC identifers: GC05P121264 GC05P121215 GC05P116379


(According to Entrez Gene, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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GeneCards Summary for FTMT Gene:
FTMT (ferritin mitochondrial) is a protein-coding gene. Diseases associated with FTMT include friedreich ataxia, and primary spontaneous pneumothorax. GO annotations related to this gene include ferric iron binding and ferroxidase activity. An important paralog of this gene is FTHL17.

UniProtKB/Swiss-Prot: FTMT_HUMAN, Q8N4E7
Function: Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Has
ferroxidase activity. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation

Gene Wiki entry for FTMT (Mitochondrial ferritin) Gene


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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RefSeq DNA sequence:
NC_000005.10  NC_018916.2  NT_034772.7  
Regulatory elements:
   Regulatory transcription factor binding sites in the FTMT gene promoter:
         c-Fos   TBP   AP-1   Pax-6   RORalpha2   YY1   AREB6   Pax-3   c-Myb   Zic3   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFTMT promoter sequence
   Search Chromatin IP Primers for FTMT

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat FTMT


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 5q21.3   Ensembl cytogenetic band:  5q23.1   HGNC cytogenetic band: 5q23.1

FTMT Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FTMT gene location

GeneLoc information about chromosome 5         GeneLoc Exon Structure

GeneLoc location for GC05P121187:  view genomic region     (about GC identifiers)

Start:
121,187,650 bp from pter      End:
121,188,528 bp from pter
Size:
879 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, 2neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
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UniProtKB/Swiss-Prot: FTMT_HUMAN, Q8N4E7 (See protein sequence)
Recommended Name: Ferritin, mitochondrial precursor  
Size: 242 amino acids; 27538 Da
Subunit: Homooligomer of 24 subunits. The functional molecule is roughly spherical and contains a central cavity
into which the polymeric mineral iron core is deposited
1 PDB 3D structure from and Proteopedia for FTMT:
1R03 (3D)    

Explore the universe of human proteins at neXtProt for FTMT: NX_Q8N4E7

Explore proteomics data for FTMT at MOPED

Selected DME Specific Peptides for FTMT (Q8N4E7) (see all 5)
 DPHLCDF  EQVKSIK  LQDIKKP  LEKNVNQ 


See FTMT Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

REFSEQ proteins: NP_803431.1  
ENSEMBL proteins: 
 ENSP00000313691  

FTMT Human Recombinant Protein Products:

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Cloud-Clone Corp. CLIAs for FTMT


(According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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Selected InterPro protein domains (see all 6):
 IPR009040 Ferritin-like_diiron
 IPR012347 Ferritin-rel
 IPR001519 Ferritin
 IPR014034 Ferritin_CS
 IPR009078 Ferritin-like_SF

Graphical View of Domain Structure for InterPro Entry Q8N4E7

ProtoNet protein and cluster: Q8N4E7

3 Blocks protein domains:
IPB001519 Ferritin
IPB008331 Ferritin and Dps
IPB014034 Ferritin


UniProtKB/Swiss-Prot: FTMT_HUMAN, Q8N4E7
Similarity: Belongs to the ferritin family
Similarity: Contains 1 ferritin-like diiron domain


FTMT for domains           About GeneDecksing


(According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
transcription factor targeting from QIAGEN and/or HOMER, miRNA Gene Targets from miRTarBase, shRNA from OriGene, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, SwitchGear Genomics, Gene Editing from DNA2.0, Clones from OriGene, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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Molecular Function:

     UniProtKB/Swiss-Prot Summary: FTMT_HUMAN, Q8N4E7
Function: Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Has
ferroxidase activity. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation
Catalytic activity: 4 Fe(2+) + 4 H(+) + O(2) = 4 Fe(3+) + 2 H(2)O

     Enzyme Number (IUBMB): EC 1.16.3.11 2

     Gene Ontology (GO): 2 molecular function terms:    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0004322ferroxidase activity IEA--
GO:0008199ferric iron binding IEA--
     
FTMT for ontologies           About GeneDecksing


Phenotypes:
     1 MGI mutant phenotype (inferred from 1 allele(MGI details for Ftmt):
 normal 

FTMT for phenotypes           About GeneDecksing

Animal Models:
     MGI mouse knock-out Ftmttm1Mdf for FTMT

   inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for FTMT
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   genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for FTMT
   genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for FTMT

miRNA
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GenScript: all cDNA clones in your preferred vector: FTMT (NM_177478)
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DNA2.0 Custom Codon Optimized Gene Synthesis Service for FTMT
Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FTMT

Cell Line
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Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FTMT


(According to UniProtKB, COMPARTMENTS Subcellular localization database, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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Subcellular locations from UniProtKB/Swiss-Prot
FTMT_HUMAN, Q8N4E7: Mitochondrion
Subcellular locations from COMPARTMENTS: 

CompartmentConfidence
mitochondrion5
cytosol1

Gene Ontology (GO): 1 cellular component term:    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0005739mitochondrion IEA--

FTMT for ontologies           About GeneDecksing


(SuperPaths according to PathCards, Pathways according to R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to QIAGEN, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene).
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SuperPaths for FTMT About    
See pathways by source

SuperPathContained pathways About
1Metabolism of porphyrins
Porphyrin and chlorophyll metabolism0.56
2Mineral absorption
Mineral absorption

Pathways by source                                                                                                                                                                 See SuperPaths
Show all pathways



2 Kegg Pathways  (Kegg details for FTMT):
    Porphyrin and chlorophyll metabolism
Mineral absorption


FTMT for pathways           About GeneDecksing

    Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for FTMT
Interactions:

    Search GeneGlobe Interaction Network for FTMT

STRING Interaction Network Preview (showing 5 interactants - click image to see 20)

Selected Interacting proteins for FTMT (ENSP000003136914) via UniProtKB, MINT, STRING, and/or I2D (see all 20)
InteractantInteraction Details
GeneCardExternal ID(s)
FECHENSP000003723264STRING: ENSP00000372326
EIF1ADENSP000003091754STRING: ENSP00000309175
MRPL50ENSP000003639994STRING: ENSP00000363999
GSTA4ENSP000003599984STRING: ENSP00000359998
NFYAENSP000003457024STRING: ENSP00000345702
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Gene Ontology (GO): Selected biological process terms (see all 6):    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0006826iron ion transport IEA--
GO:0006879cellular iron ion homeostasis IDA18160053
GO:0008284positive regulation of cell proliferation IDA18160053
GO:0051347positive regulation of transferase activity IDA18160053
GO:0051349positive regulation of lyase activity IDA18160053

FTMT for ontologies           About GeneDecksing



(Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience, ApexBio, HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB)
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Browse Small Molecules at EMD Millipore
   Browse drugs & compounds from Enzo Life Sciences
  Browse compounds at ApexBio 

Browse Tocris compounds for FTMT

4 HMDB Compounds for FTMT    About this table
CompoundSynonyms CAS #PubMed Ids
CopperCu (see all 2)7440-50-8--
IronArmco iron (see all 19)7439-89-6--
OxygenOxygen (see all 5)7782-44-7--
WaterDihydrogen oxide (see all 2)7732-18-5--

7 Novoseek inferred chemical compound relationships for FTMT gene    About this table
Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
iron 70.5 100 12547228 (9), 18691669 (8), 18815198 (7), 15282205 (6) (see all 26)
ferric ammonium citrate 70.3 5 10691965 (4)
deferoxamine 50.7 5 10691965 (4)
iron-sulfur 38.5 1 15282205 (1)
endotoxin 31.8 6 11469787 (1), 12801518 (1), 11429389 (1), 12139748 (1)
sulfur 14 2 18560166 (1), 18560167 (1)
atp 9.05 2 11033347 (1), 18815198 (1)



FTMT for compounds           About GeneDecksing



(Secondary structures according to fRNAdb,
GenBank/EMBL/DDBJ Accessions according to
Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
RefSeq according to Entrez Gene,
DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
Conferences by KenesGroup, exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, and/or QIAGEN )
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REFSEQ mRNAs for FTMT gene: 
NM_177478.1  

Unigene Cluster for FTMT:

Ferritin mitochondrial
Hs.105324  [show with all ESTs]
Unigene Representative Sequence: NM_177478
1 Ensembl transcript including schematic representation, and UCSC links where relevant:
ENST00000321339(uc003kss.3)

miRNA
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Search for qRT-PCR Assays for microRNAs that regulate FTMT
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Inhib. RNA
Products:
     
OriGene RNAi products in human, mouse, rat for FTMT
Predesigned siRNA for gene silencing in human, mouse, rat FTMT
Clone
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GenScript: all cDNA clones in your preferred vector: FTMT (NM_177478)
DNA2.0 Custom Codon Optimized Gene Synthesis Service for FTMT
Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FTMT
Primer
Products:
    
OriGene qPCR primer pairs and template standards for FTMT
OriGene qSTAR qPCR primer pairs in human, mouse for FTMT
Pre-validated RT2 qPCR Primer Assay in human, mouse, rat FTMT
  QuantiTect SYBR Green Assays in human, mouse, rat FTMT
  QuantiFast Probe-based Assays in human, mouse, rat FTMT

Additional mRNA sequence: BC034419.1 

1 DOTS entry:

DT.95302809 

7 AceView cDNA sequences:

NM_177478 AA469940 AA470110 BC034419 BX116510 AI024273 AI149710 

GeneLoc Exon Structure


(RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MaxQB, plus additional links to SOURCE, and/or BioGPS, and/or UniProtKB,
PCR Arrays from QIAGEN, Primers from OriGene, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
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FTMT expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS <intensity>2/3
CGAP TAG: GAGTGTGCTC
FTMT Expression
About this image

FTMT Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

FTMT Protein Expression

SOURCE GeneReport for Unigene cluster: Hs.105324

UniProtKB/Swiss-Prot: FTMT_HUMAN, Q8N4E7
Tissue specificity: Detected in testis and erythroleukemia. Expression is very low or not detectable in brain,
colon, heart, kidney, liver, lung, muscle, placental, spleen and small intestine

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In Situ
Assay Products:
 

 
Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FTMT

(Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
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This gene was present in the common ancestor of animals.

Orthologs for FTMT gene from Selected species (see all 11)    About this table
Organism Taxonomic
classification
Gene Description Human
Similarity
Orthology
Type
Details
mouse
(Mus musculus)
Mammalia Ftmt1 , 5 ferritin mitochondrial1, 5 78.76(n)1
77.64(a)1
  18 (28.19 cM)5
676341  NM_026286.31  NP_080562.21 
 523315365 
chicken
(Gallus gallus)
Aves FTH6
Gallus gallus ferritin, heavy polypeptide 1 (FTH1)...
77(a)
1 → many
5(16149680-16154242)
lizard
(Anolis carolinensis)
Reptilia --
--
78(a)
1 → many
GL343235.1(2273171-2283525)
zebrafish
(Danio rerio)
Actinopterygii zgc:920661 zgc:92066 67.84(n)
67.65(a)
  436651  NM_001002378.1  NP_001002378.1 
fruit fly
(Drosophila melanogaster)
Insecta Fer3HCH1 Ferritin 3 heavy chain homologue 54.12(n)
46.3(a)
  32260  NM_132626.2  NP_572854.1 


ENSEMBL Gene Tree for FTMT (if available)
TreeFam Gene Tree for FTMT (if available)

(Paralogs according to 1HomoloGene,
2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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Paralogs for FTMT gene
FTHL172  FTH12  FTL2  
4 SIMAP similar genes for FTMT using alignment to 1 protein entry:     FTMT_HUMAN:
FTH1    FTH1P19    FTHL17    FTL

FTMT for paralogs           About GeneDecksing


1 Pseudogenes.org Pseudogene for FTMT
PGOHUM00000244158


(SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD), the Human Cytochrome P450 Allele Nomenclature Database, and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers, Cancer Mutation PCR Arrays and Assays, and Copy Number PCR Arrays from QIAGEN)
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Selected SNPs for FTMT (see all 94)    About this table    
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 5 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs1898421891,2
--121185800(+) TACTTC/TAATGC 1 -- us2k10--------
rs1810634021,2
--121185801(+) ACTTCA/GATGCA 1 -- us2k10--------
rs1121503191,2
C,F--121185803(+) TTCAAC/TGCAAA 1 -- us2k11Minor allele frequency- T:0.50CSA 2
rs1863059461,2
--121185829(+) AACACA/CAGCAC 1 -- us2k10--------
rs1914987631,2
--121185931(+) ACACTA/CTGCTG 1 -- us2k10--------
rs1382546511,2
C--121186020(+) TAATCC/TGGCTT 1 -- us2k10--------
rs1832908741,2
--121186067(+) TCTGAC/TCACAG 1 -- us2k10--------
rs1427569051,2
--121186214(+) AGGAAC/TTACTG 1 -- us2k10--------
rs1461050631,2
--121186235(+) CAGTGC/TGGATG 1 -- us2k10--------
rs1874004431,2
--121186255(+) ATAATC/TACACT 1 -- us2k10--------

HapMap Linkage Disequilibrium report for FTMT (121187650 - 121188528 bp)

Structural Variations
     Database of Genomic Variants (DGV) 1 variation for FTMT:    About this table    
Variant IDTypeSubtypePubMed ID
nsv830469CNV Gain17160897

Human Gene Mutation Database (HGMD): FTMT
Site Specific Mutation Identification with PCR Assays
Search QIAGEN SeqTarget long-range PCR primers for resequencing FTMT
DNA2.0 Custom Variant and Variant Library Synthesis for FTMT

(in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
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OMIM gene information: 608847    OMIM disorders: --

14 diseases for FTMT:    
About MalaCards
friedreich ataxia    primary spontaneous pneumothorax    myelodysplastic syndromes    spontaneous pneumothorax
sideroblastic anemia    age related macular degeneration    pneumothorax    restless legs syndrome
cerebritis    ataxia    hypoxia    melanoma
alzheimer's disease    ovarian cancer

1 disease from the University of Copenhagen DISEASES database for FTMT:
Friedreich ataxia

FTMT for disorders           About GeneDecksing


Congresses - knowledge worth sharing:
Alzheimer's & Parkinson's Diseases Congress (ADPD) 18 - 22 March 2015

9 Novoseek inferred disease relationships for FTMT gene    About this table

Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
anemia sideroblastic 87.8 6 12406866 (4), 15282205 (1), 18160053 (1)
friedreich ataxia 80.2 2 18815198 (2)
anemia refractory 48.3 1 12406866 (1)
cerebral vasospasm 43.2 1 11680510 (1)
iron overload 42.8 3 15282205 (2), 15747401 (1)
melanoma 37.6 17 19017294 (5), 8836133 (3), 10691965 (3), 11033347 (2) (see all 7)
myelodysplastic syndromes 33.7 1 15755901 (1)
vasospasm 29.9 4 9303007 (3)
cerebral infarction 21.6 2 9303007 (2)

Genetic Association Database (GAD): FTMT
Human Genome Epidemiology (HuGE) Navigator: FTMT (2 documents)

Export disorders for FTMT gene to outside databases

(in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
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PubMed articles for FTMT gene, integrated from 10 sources (see all 74):
(articles sorted by number of sources associating them with FTMT)
    Utopia: connect your pdf to the dynamic
world of online information

  1. A human mitochondrial ferritin encoded by an intronless gene. (PubMed id 11323407)1, 2, 3, 9 Levi S.... Drysdale J. (J. Biol. Chem. 2001)
  2. Crystal structure and biochemical properties of the human mitochondrial ferritin and its mutant Ser144Ala. (PubMed id 15201052)1, 2, 9 Langlois d'Estaintot B.... Arosio P. (J. Mol. Biol. 2004)
  3. Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression. (PubMed id 20877624)1, 4 Hendrickson S.L....O'Brien S.J. (PLoS ONE 2010)
  4. Sequence variations in mitochondrial ferritin: distribution in healthy controls and different types of patients. (PubMed id 20939738)1, 4 Castiglioni E....Arosio P. (Genet Test Mol Biomarkers 2010)
  5. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S.... Malek J. (Genome Res. 2004)
  6. Mitochondrial ferritin: a new player in iron metabolism. (PubMed id 12547228)1, 9 Drysdale J....Levi S. (amp 2002)
  7. Mitochondrial ferritin limits oxidative damage regulating mitochondrial iron availability: hypothesis for a protective role in Friedreich ataxia. (PubMed id 18815198)1, 9 Campanella A....Levi S. (Hum. Mol. Genet. 2009)
  8. Unique iron binding and oxidation properties of human mitochondrial ferritin: a comparative analysis with Human H-chain ferritin. (PubMed id 15755449)1, 9 Bou-Abdallah F....Chasteen N.D. (J. Mol. Biol. 2005)
  9. Mitochondrial ferritin in the substantia nigra in restless legs syndrome. (PubMed id 19816198)1, 9 Snyder A.M....Connor J.R. (J. Neuropathol. Exp. Neurol. 2009)
  10. Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia. (PubMed id 12406866)1, 9 Cazzola M....Arosio P. (Blood 2003)

(in PubMed, OMIM, and NCBI Bookshelf)
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Aliases
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  Query String
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(According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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Entrez Gene: 94033 HGNC: 17345 AceView: FTMT Ensembl:ENSG00000181867 euGenes: HUgn94033
ECgene: FTMT Kegg: 94033 H-InvDB: FTMT

(According to HUGE)
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(According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
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NameDescription
PharmGKB entry for FTMT Pharmacogenomics, SNPs, Pathways
Wikipedia http://en.wikipedia.org/wiki/Ferritin

(Patent information from GeneIP,
Licensable technologies from WIS Yeda, Salk, Tufts,
IP news from LifeMap Sciences, Inc.)
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Patent Information for FTMT gene:
Search GeneIP for patents involving FTMT

GeneCards and IP:
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(Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, and ESI BIO, PCR Arrays from QIAGEN, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, Enzo Life Sciences, and/or ApexBio, In Situ Hybridization Assays from
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