This gene encodes a member of the non-metastatic expressed family of nucleoside diphosphate kinases. Members of this family are enzymes that catalyzes phosphate transfer from nucleoside triphosphates to nucleoside diphosphates. This protein contains two kinase domains, one of which is involved in autophosphorylation and the other may be inactive. This protein localizes to the c... See more...

Aliases for NME7 Gene

Aliases for NME7 Gene

  • NME/NM23 Family Member 7 2 3 5
  • Non-Metastatic Cells 7, Protein Expressed In (Nucleoside-Diphosphate Kinase) 2 3
  • Cilia And Flagella Associated Protein 67 2 3
  • Nucleoside Diphosphate Kinase 7 3 4
  • NDP Kinase 7 3 4
  • EC 4 50
  • Nm23-H7 3 4
  • CFAP67 2 3
  • NDK 7 3 4
  • FLJ37194 2
  • NM23-H7 2
  • MN23H7 3
  • NDK7 3
  • NME7 5

External Ids for NME7 Gene

Previous GeneCards Identifiers for NME7 Gene

  • GC01P166788
  • GC01M164752
  • GC01M165797
  • GC01M166289
  • GC01M165833
  • GC01M167368
  • GC01M140347

Summaries for NME7 Gene

Entrez Gene Summary for NME7 Gene

  • This gene encodes a member of the non-metastatic expressed family of nucleoside diphosphate kinases. Members of this family are enzymes that catalyzes phosphate transfer from nucleoside triphosphates to nucleoside diphosphates. This protein contains two kinase domains, one of which is involved in autophosphorylation and the other may be inactive. This protein localizes to the centrosome and functions as a component of the gamma-tubulin ring complex which plays a role in microtubule organization. Mutations in this gene may be associated with venous thromboembolism. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]

GeneCards Summary for NME7 Gene

NME7 (NME/NM23 Family Member 7) is a Protein Coding gene. Diseases associated with NME7 include Dextrocardia With Situs Inversus and Deafness, Autosomal Dominant 7. Among its related pathways are superpathway of pyrimidine deoxyribonucleotides de novo biosynthesis and purine nucleotides de novo biosynthesis. Gene Ontology (GO) annotations related to this gene include nucleoside diphosphate kinase activity. An important paralog of this gene is NME8.

UniProtKB/Swiss-Prot Summary for NME7 Gene

  • Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate.

No data available for CIViC Summary , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , Rfam classification and piRNA Summary for NME7 Gene

Genomics for NME7 Gene

GeneHancer (GH) Regulatory Elements Pubs

Promoters and enhancers for NME7 Gene
GeneHancer (GH) Identifier GH Type GH
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH01J169362 Promoter/Enhancer 2.4 EPDnew Ensembl ENCODE CraniofacialAtlas dbSUPER 287.8 +1.6 1646 7.8 SP1 ZNF207 NCOR1 MYC IKZF1 SSRP1 JUND ZNF580 YY1 MXD4 NME7 BLZF1 CCDC181 C1orf112 METTL18 piR-43676-003 ATP1B1
GH01J169311 Enhancer 1.1 Ensembl ENCODE 36.4 +55.5 55547 1.2 MYC NCOR1 JUND ZNF592 ZNF10 CEBPB REST HES1 BHLHE40 ZNF639 NME7 CCDC181 lnc-CCDC181-2 piR-58929-007 ENSG00000235575 ATP1B1
GH01J169338 Enhancer 0.9 Ensembl ENCODE 42.8 +29.1 29148 0.8 NCOR1 ZNF592 TAL1 ZNF316 NFE2 RELA STAT5A SMARCA4 NFE2L2 FOXM1 NME7 ENSG00000235575 ATP1B1 LOC101928596 piR-34697-003 piR-43676-003
GH01J169308 Promoter/Enhancer 1.2 Ensembl ENCODE 32.1 +58.6 58597 1.9 NCOR1 ZNF592 NFIC REST HES1 MBD2 TBP ARNT IRF2 TAF9B NME7 RN7SL333P METTL18 C1orf112 SCYL3 DPT ATP1B1 LOC101928596 lnc-CCDC181-2 piR-58929-007
GH01J169427 Promoter/Enhancer 1.7 EPDnew Ensembl ENCODE CraniofacialAtlas 21.2 -59.3 -59253 2 ZNF600 ZNF580 ZNF223 SIN3A YY1 BHLHE40 ZNF189 NRF1 TAF1 CBX2 CCDC181 NME7 piR-33998-001 lnc-SLC19A2-1 BLZF1
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around NME7 on the GeneHancer Hub at the UCSC Golden Path

Cistromic (ChIP-Seq) regulation report from SPP (The Signaling Pathways Project) for NME7

Top Transcription factor binding sites by QIAGEN in the NME7 gene promoter:
  • ATF6
  • COMP1
  • CUTL1
  • Egr-2
  • En-1
  • Nkx2-2
  • p53
  • STAT1
  • STAT1alpha
  • STAT1beta

Genomic Locations for NME7 Gene

Latest Assembly
235,418 bases
Minus strand

Previous Assembly
(GRCh37/hg19 by Entrez Gene)
235,267 bases
Minus strand

(GRCh37/hg19 by Ensembl)
235,437 bases
Minus strand

Genomic View for NME7 Gene

Genes around NME7 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
NME7 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for NME7 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for NME7 Gene

Proteins for NME7 Gene

  • Protein details for NME7 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Recommended name:
    Nucleoside diphosphate kinase 7
    Protein Accession:
    Secondary Accessions:
    • A8K3T6
    • A8MY09
    • B3KSW9
    • Q5TGZ4

    Protein attributes for NME7 Gene

    376 amino acids
    Molecular mass:
    42492 Da
    Name=Mg(2+); Xref=ChEBI:CHEBI:18420;
    Quaternary structure:
    No Data Available

    Alternative splice isoforms for NME7 Gene


neXtProt entry for NME7 Gene

Selected DME Specific Peptides for NME7 Gene


Post-translational modifications for NME7 Gene

  • Ubiquitination at Lys51
  • Modification sites at PhosphoSitePlus

Other Protein References for NME7 Gene

Domains & Families for NME7 Gene

Gene Families for NME7 Gene

Human Protein Atlas (HPA):
  • Enzymes
  • Predicted intracellular proteins

Protein Domains for NME7 Gene

  • Nucleoside diphosphate kinase
  • Protein of unknown function DM10

Suggested Antigen Peptide Sequences for NME7 Gene

GenScript: Design optimal peptide antigens:
  • cDNA FLJ58336, highly similar to Nucleoside diphosphate kinase 7 (EC (B4DXC8_HUMAN)
  • nm23-H7 (NDK7_HUMAN)

Graphical View of Domain Structure for InterPro Entry



  • Belongs to the NDK family.
  • Belongs to the NDK family.
genes like me logo Genes that share domains with NME7: view

Function for NME7 Gene

Molecular function for NME7 Gene

UniProtKB/Swiss-Prot Function:
Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate.
UniProtKB/Swiss-Prot CatalyticActivity:
Reaction=a 2'-deoxyribonucleoside 5'-diphosphate + ATP = a 2'-deoxyribonucleoside 5'-triphosphate + ADP; Xref=Rhea:RHEA:44640, ChEBI:CHEBI:30616, ChEBI:CHEBI:61560, ChEBI:CHEBI:73316, ChEBI:CHEBI:456216; EC=;.
UniProtKB/Swiss-Prot CatalyticActivity:
Reaction=a ribonucleoside 5'-diphosphate + ATP = a ribonucleoside 5'-triphosphate + ADP; Xref=Rhea:RHEA:18113, ChEBI:CHEBI:30616, ChEBI:CHEBI:57930, ChEBI:CHEBI:61557, ChEBI:CHEBI:456216; EC=;.

Enzyme Numbers (IUBMB) for NME7 Gene

Phenotypes From GWAS Catalog for NME7 Gene

Gene Ontology (GO) - Molecular Function for NME7 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000166 nucleotide binding IEA --
GO:0004550 nucleoside diphosphate kinase activity IEA --
GO:0005515 protein binding IPI 16189514
GO:0005524 ATP binding IEA --
GO:0016301 kinase activity IEA --
genes like me logo Genes that share ontologies with NME7: view
genes like me logo Genes that share phenotypes with NME7: view

Animal Models for NME7 Gene

MGI Knock Outs for NME7:
  • Nme7 Nme7<tm2b(EUCOMM)Hmgu>

Animal Models for research

  • Taconic Biosciences Mouse Models for NME7

miRNA for NME7 Gene

miRTarBase miRNAs that target NME7

Inhibitory RNAs for research

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for NME7

No data available for Human Phenotype Ontology , Transcription Factor Targets and HOMER Transcription for NME7 Gene

Localization for NME7 Gene

Subcellular locations from

Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for NME7 gene
Compartment Confidence
cytoskeleton 5
cytosol 5
mitochondrion 3
plasma membrane 2
nucleus 2
extracellular 1
endoplasmic reticulum 1
lysosome 1
golgi apparatus 1

Subcellular locations from the

Human Protein Atlas (HPA)

Gene Ontology (GO) - Cellular Components for NME7 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005813 centrosome IBA,IDA 21399614
GO:0005829 cytosol TAS --
genes like me logo Genes that share ontologies with NME7: view

No data available for Subcellular locations from UniProtKB/Swiss-Prot for NME7 Gene

Pathways & Interactions for NME7 Gene

genes like me logo Genes that share pathways with NME7: view

Gene Ontology (GO) - Biological Process for NME7 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0006165 nucleoside diphosphate phosphorylation IEA --
GO:0006183 GTP biosynthetic process IEA --
GO:0006228 UTP biosynthetic process IEA --
GO:0006241 CTP biosynthetic process IEA --
GO:0009117 nucleotide metabolic process IEA --
genes like me logo Genes that share ontologies with NME7: view

No data available for SIGNOR curated interactions for NME7 Gene

Drugs & Compounds for NME7 Gene

(12) Drugs for NME7 Gene - From: HMDB

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Magnesium Approved, Experimental, Investigational Pharma 0
CDP Experimental Pharma 0
Cytidine triphosphate Experimental Pharma 0
dATP Experimental Pharma 0
dctp Experimental Pharma 0

(11) Additional Compounds for NME7 Gene - From: HMDB

Name Synonyms Role CAS Number PubChem IDs PubMed IDs
2'-Deoxyinosine triphosphate
  • 2'-Deoxyinosine 5'-triphosphate
  • 2'-Deoxyinosine-5'-triphosphate
  • Deoxyinosine 5'-triphosphate
  • 2'-Deoxyinosine 5'-triphosphoric acid
  • 2'-Deoxyinosine-5'-triphosphoric acid
  • 5'-Adenylphosphoric acid
  • Adenosine 5'-diphosphate
  • ADENOSINE-5'-diphosphATE
  • H3ADP
  • 5'-Adenylphosphate
  • 2'-Deoxyadenosine-5'-diphosphate
  • Deoxyadenosine diphosphate
  • 2'-Deoxycytidine 5'-diphosphate
  • 2'-Deoxycytidine diphosphate
  • D-1beta-Ribofuranosylcytosine diphosphate
  • Deoxycytidine diphosphate
  • 2'-Deoxycytidine 5'-diphosphoric acid
Deoxyuridine triphosphate
  • 2'-Deoxyuridine 5'-triphosphate
  • 2'-Deoxyuridine 5'-triphosphoric acid
  • Deoxyuridine triphosphoric acid
  • 2'-Deoxyuridine-5'-triphosphorate
  • 2'-Deoxyuridine-5'-triphosphoric acid
genes like me logo Genes that share compounds with NME7: view

Transcripts for NME7 Gene

mRNA/cDNA for NME7 Gene

8 NCBI additional mRNA sequence :
14 Ensembl transcripts including schematic representations, and UCSC links to gene/alias where relevant :

Inhibitory RNAs for research

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for NME7

Alternative Splicing Database (ASD) splice patterns (SP) for NME7 Gene

No ASD Table

Relevant External Links for NME7 Gene

GeneLoc Exon Structure for

Expression for NME7 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and SAGE for NME7 Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

Protein differential expression in normal tissues from HIPED for NME7 Gene

This gene is overexpressed in Breast (27.4), Bone (8.1), Neutrophil (8.0), and Pancreatic juice (7.6).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, MaxQB, and MOPED for NME7 Gene

Transcriptomic regulation report from SPP (The Signaling Pathways Project) for NME7

SOURCE GeneReport for Unigene cluster for NME7 Gene:


Evidence on tissue expression from TISSUES for NME7 Gene

  • Nervous system(4.8)
  • Lung(4.5)
  • Blood(4.4)
  • Kidney(2.6)
genes like me logo Genes that share expression patterns with NME7: view

No data available for mRNA differential expression in normal tissues , Protein tissue co-expression partners , mRNA Expression by UniProt/SwissProt and Phenotype-based relationships between genes and organs from Gene ORGANizer for NME7 Gene

Orthologs for NME7 Gene

This gene was present in the common ancestor of animals and fungi.

Orthologs for NME7 Gene

Organism Taxonomy Gene Similarity Type Details
(Pan troglodytes)
Mammalia NME7 29 30
  • 99.73 (n)
(Canis familiaris)
Mammalia NME7 29 30
  • 92.38 (n)
(Bos Taurus)
Mammalia NME7 29 30
  • 91.49 (n)
(Mus musculus)
Mammalia Nme7 29 16 30
  • 85.42 (n)
(Rattus norvegicus)
Mammalia Nme7 29
  • 84.36 (n)
(Ornithorhynchus anatinus)
Mammalia NME7 30
  • 81 (a)
(Monodelphis domestica)
Mammalia NME7 30
  • 78 (a)
(Gallus gallus)
Aves NME7 29 30
  • 76.53 (n)
(Anolis carolinensis)
Reptilia NME7 30
  • 65 (a)
Tropical Clawed Frog
(Silurana tropicalis)
Amphibia nme7 29
  • 68.79 (n)
MGC75677 29
(Danio rerio)
Actinopterygii nme7 29 30
  • 65.5 (n)
ndpkz4 29
Rainbow Trout
(Oncorhynchus mykiss)
Actinopterygii Omy.6857 29
African malaria mosquito
(Anopheles gambiae)
Insecta AgaP_AGAP003227 29
  • 49.58 (n)
Fruit Fly
(Drosophila melanogaster)
Insecta nmdyn-D7 29 30 31
  • 48.94 (n)
Baker's yeast
(Saccharomyces cerevisiae)
Saccharomycetes YNK1 30
  • 29 (a)
Sea Squirt
(Ciona savignyi)
Ascidiacea -- 30
  • 50 (a)
Sea Vase
(Ciona intestinalis)
Ascidiacea Cin.25 29
Species where no ortholog for NME7 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Eremothecium gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • Alicante grape (Vitis vinifera)
  • Alpha proteobacteria (Wolbachia pipientis)
  • Amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • Barley (Hordeum vulgare)
  • Beta proteobacteria (Neisseria meningitidis)
  • Bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • Common water flea (Daphnia pulex)
  • Corn (Zea mays)
  • E. coli (Escherichia coli)
  • Filamentous fungi (Aspergillus nidulans)
  • Firmicute Bacteria (Streptococcus pneumoniae)
  • Fission Yeast (Schizosaccharomyces pombe)
  • Green Algae (Chlamydomonas reinhardtii)
  • Honey Bee (Apis mellifera)
  • K. Lactis Yeast (Kluyveromyces lactis)
  • Loblloly Pine (Pinus taeda)
  • Malaria Parasite (Plasmodium falciparum)
  • Medicago Trunc (Medicago Truncatula)
  • Moss (Physcomitrella patens)
  • Orangutan (Pongo pygmaeus)
  • Pig (Sus scrofa)
  • Rice (Oryza sativa)
  • Rice Blast Fungus (Magnaporthe grisea)
  • Schistosome Parasite (Schistosoma mansoni)
  • Sea Anemone (Nematostella vectensis)
  • Sea Urchin (Strongylocentrotus purpuratus)
  • Sorghum (Sorghum bicolor)
  • Soybean (Glycine max)
  • Stem Rust Fungus (Puccinia graminis)
  • Sugarcane (Saccharum officinarum)
  • Thale Cress (Arabidopsis thaliana)
  • Tomato (Lycopersicon esculentum)
  • Toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • Wheat (Triticum aestivum)
  • Worm (Caenorhabditis elegans)

Evolution for NME7 Gene

Gene Tree for NME7 (if available)
Gene Tree for NME7 (if available)
Evolutionary constrained regions (ECRs) for NME7: view image
Alliance of Genome Resources:
Additional Orthologs for NME7

Paralogs for NME7 Gene

Paralogs for NME7 Gene

(8) SIMAP similar genes for NME7 Gene using alignment to 3 proteins:

genes like me logo Genes that share paralogs with NME7: view

Variants for NME7 Gene

Sequence variations, with clinical significance, from ClinVar and Humsavar, with links to dbSNP for NME7 Gene

SNP ID Clinical significance and condition Chr 01 pos Variation AA Info Type
rs267598155 Uncertain Significance: Cardiac arrhythmia 169,130,013(-) C/T
NM_001677.4(ATP1B1):c.571C>T (p.Pro191Ser)

dbSNP identifiers (rs#s) for variants without ClinVar clinical significance for NME7 Gene

All consequence types are included: molecular consequences (e.g. missense, synonymous), and location-based (e.g. intron, upstream).

Structural Variations from Database of Genomic Variants (DGV) for NME7 Gene

Variant ID Type Subtype PubMed ID
dgv112e212 CNV loss 25503493
dgv113e212 CNV loss 25503493
dgv114e212 CNV gain 25503493
dgv115e212 CNV gain 25503493
dgv42n27 CNV loss 19166990
dgv459n100 CNV gain 25217958
dgv625n54 CNV loss 21841781
dgv626n54 CNV gain+loss 21841781
dgv627n54 CNV gain 21841781
dgv628n54 CNV gain 21841781
dgv629n54 CNV loss 21841781
dgv630n54 CNV loss 21841781
dgv78e199 CNV deletion 23128226
esv1001229 CNV deletion 20482838
esv1007713 CNV loss 20482838
esv1106459 CNV deletion 17803354
esv1514014 CNV deletion 17803354
esv1584020 CNV insertion 17803354
esv1749280 CNV deletion 17803354
esv22143 CNV gain+loss 19812545
esv2421693 CNV deletion 20811451
esv2674167 CNV deletion 23128226
esv2677177 CNV deletion 23128226
esv2677260 CNV deletion 23128226
esv2719350 CNV deletion 23290073
esv2719362 CNV deletion 23290073
esv2719373 CNV deletion 23290073
esv2761410 CNV loss 21179565
esv2764197 CNV loss 21179565
esv2848902 CNV deletion 24192839
esv3008234 CNV deletion 24192839
esv32640 CNV gain+loss 17666407
esv33347 CNV loss 17666407
esv3542356 CNV deletion 23714750
esv3575272 CNV gain 25503493
esv3575283 CNV gain 25503493
esv3587879 CNV loss 21293372
esv3587880 CNV loss 21293372
esv3587881 CNV loss 21293372
esv3890760 CNV loss 25118596
esv4017 CNV loss 18987735
esv5790 CNV loss 19470904
esv993090 CNV deletion 20482838
nsv1004674 CNV gain 25217958
nsv1010010 CNV gain 25217958
nsv1068314 CNV deletion 25765185
nsv1078878 OTHER inversion 25765185
nsv1122418 CNV deletion 24896259
nsv1124598 CNV duplication 24896259
nsv1161886 OTHER complex 26073780
nsv159064 CNV insertion 16902084
nsv442352 CNV loss 18776908
nsv477399 CNV novel sequence insertion 20440878
nsv508044 OTHER sequence alteration 20534489
nsv508637 CNV deletion 20534489
nsv511149 CNV loss 21212237
nsv514015 CNV loss 21397061
nsv515530 CNV gain+loss 19592680
nsv525520 CNV loss 19592680
nsv548157 CNV gain 21841781
nsv548164 CNV loss 21841781
nsv548183 CNV gain+loss 21841781
nsv548186 CNV loss 21841781
nsv818567 CNV gain+loss 17921354
nsv820118 CNV gain 19587683
nsv820717 CNV deletion 20802225
nsv825376 CNV loss 20364138
nsv825387 CNV gain 20364138
nsv825398 CNV gain 20364138
nsv831858 CNV gain 17160897
nsv831871 CNV loss 17160897
nsv947448 CNV deletion 23825009
nsv958041 CNV deletion 24416366

Variation tolerance for NME7 Gene

Residual Variation Intolerance Score: 73.1% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 2.22; 40.04% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for NME7 Gene

Human Gene Mutation Database (HGMD)
SNPedia medical, phenotypic, and genealogical associations of SNPs for
Leiden Open Variation Database (LOVD)

SNP Genotyping and Copy Number Assays for research

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for NME7 Gene

Disorders for NME7 Gene

MalaCards: The human disease database

(5) MalaCards diseases for NME7 Gene - From: ORP and COP

Disorder Aliases PubMed IDs
dextrocardia with situs inversus
  • situs inversus totalis
deafness, autosomal dominant 7
  • dfna7
renal glucosuria
  • glys
visceral heterotaxy
  • heterotaxia
primary ciliary dyskinesia
  • ciliary motility disorder
- elite association - COSMIC cancer census association via MalaCards
Search NME7 in MalaCards View complete list of genes associated with diseases

Additional Disease Information for NME7

Human Genome Epidemiology Navigator
ATLAS of Genetics and Cytogenetics in Oncology and Haematology
Open Targets Platform
Open Targets Platform
genes like me logo Genes that share disorders with NME7: view

No data available for UniProtKB/Swiss-Prot and Genatlas for NME7 Gene

Publications for NME7 Gene

  1. A Homozygous Nme7 Mutation Is Associated with Situs Inversus Totalis. (PMID: 27060491) Reish O … Parvari R (Human mutation 2016) 3 72
  2. Genetic predictors of fibrin D-dimer levels in healthy adults. (PMID: 21502573) Smith NL … Hayward C (Circulation 2011) 3 40
  3. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PMID: 20379614) Rose JE … Uhl GR (Molecular medicine (Cambridge, Mass.) 2010) 3 40
  4. Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling. (PMID: 19240061) Trynka G … Wijmenga C (Gut 2009) 3 40
  5. Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation. (PMID: 19064610) Cheung CL … Kung AW (Human molecular genetics 2009) 3 40

Products for NME7 Gene

Sources for NME7 Gene