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MTRNR2L10 Gene

protein-coding   GIFtS: 25
GCID: GC0XM055274

MT-RNR2-Like 10

  See MTRNR2L10-related disease
at  

(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
MT-RNR2-Like 101 2
Humanin-Like 101 2
HN102 3
Humanin-Like Protein 102
MTRNR2-Like 102
MT-RNR2-Like Protein 103

External Ids:    HGNC: 371671   Entrez Gene: 1004634882   Ensembl: ENSG000002560457   UniProtKB: P0CJ773   

Export aliases for MTRNR2L10 gene to outside databases

Previous GC identifers: GC0XU901540 GC0XM055217 GC0XM055243 GC0XM055247 GC0XM055253 GC0XM055261 GC0XM055266 GC0XM055270


(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 MTRNR2L10 Gene:
MTRNR2L10 (MT-RNR2-like 10) is a protein-coding gene. Diseases associated with MTRNR2L10 include alzheimer's disease.

UniProtKB/Swiss-Prot: HMN10_HUMAN, P0CJ77
Function: Plays a role as a neuroprotective and antiapoptotic factor (By similarity)




(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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Regulatory elements:
   Search for regulatory transcription factor binding sites for MTRNR2L10
         Other transcription factors

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Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing in human, mouse, rat MTRNR2L10


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

Entrez Gene cytogenetic band: Xp11.21   Ensembl cytogenetic band:  Xp11.21   HGNC cytogenetic band: Xp11.21

MTRNR2L10 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
MTRNR2L10 gene location

GeneLoc information about chromosome X         GeneLoc Exon Structure

GeneLoc location for GC0XM055274:  view genomic region     (about GC identifiers)

Start:
55,207,824 bp from pter      End:
55,208,944 bp from pter
Size:
1,121 bases      Orientation:
minus 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, Cloud-Clone Corp., and/or eBioscience,
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UniProtKB/Swiss-Prot: HMN10_HUMAN, P0CJ77 (See protein sequence)
Recommended Name: Humanin-like protein 10  
Size: 24 amino acids; 2806 Da

Explore the universe of human proteins at neXtProt for MTRNR2L10: NX_P0CJ77

REFSEQ proteins: NP_001177637.1  
ENSEMBL proteins: 
 ENSP00000442159  

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(According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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1 InterPro protein domain:
 IPR028139 Humanin

Graphical View of Domain Structure for InterPro Entry P0CJ77

ProtoNet protein and cluster: P0CJ77

UniProtKB/Swiss-Prot: HMN10_HUMAN, P0CJ77
Similarity: Belongs to the humanin family


Find genes that share domains with MTRNR2L10           About GenesLikeMe


(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, Vector BioLabs and/or Addgene, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Flow cytometry from eBioscience, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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Molecular Function:

     UniProtKB/Swiss-Prot Summary: HMN10_HUMAN, P0CJ77
Function: Plays a role as a neuroprotective and antiapoptotic factor (By similarity)
Induction: Down-regulated 6 hours following staurosporine (STS) treatment and up-regulated 24 hours following STS
treatment. Down-regulated 6 hours following beta-carotene treatment, while it is up-regulated 24 hours following
beta-carotene treatment

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(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
HMN10_HUMAN, P0CJ77: Cytoplasm (By similarity). Secreted (By similarity)

Gene Ontology (GO): 2 cellular component terms:    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0005576extracellular region IEA--
GO:0005737cytoplasm IEA--

Find genes that share ontologies with MTRNR2L10           About GenesLikeMe


(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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(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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(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,
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, and/or Addgene, Primers from OriGene, and/or QIAGEN, Flow cytometry from eBioscience )
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REFSEQ mRNAs for MTRNR2L10 gene: 
NM_001190708.1  

1 Ensembl transcript including schematic representation, and UCSC links where relevant:
ENST00000545075(uc022bxr.1)
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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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MTRNR2L10 expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS <intensity>2/3
CGAP TAG: AGAATTCTCA
MTRNR2L10 Expression
About this image

MTRNR2L10 Protein expression data from MOPED1, PaxDb2 and MaxQB3 --

UniProtKB/Swiss-Prot: HMN10_HUMAN, P0CJ77
Tissue specificity: Expressed in mature brain, thyroid gland and testis

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(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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  --

ENSEMBL Gene Tree for MTRNR2L10 (if available)
TreeFam Gene Tree for MTRNR2L10 (if available)

(Paralogs according to 1HomoloGene,
2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
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Paralogs for MTRNR2L10 gene
2 SIMAP similar genes for MTRNR2L10 using alignment to 1 protein entry:     HMN10_HUMAN:
MTRNR2L7    MTRNR2L13

Find genes that share paralogs with MTRNR2L10           About GenesLikeMe



(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 MTRNR2L10 (see all 79)    About this table                                 

Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr X posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs1850338161,2
--55207358(+) AGCTCA/GTGATG 1 -- ds50010--------
rs1395591951,2
C--55207364(+) TGATGC/TGCCAA 1 -- ds50010--------
rs1890718671,2
--55207547(+) AAAGGG/TTAATA 1 -- ds50010--------
rs1817301901,2
C--55207554(+) AATAGC/TAGATG 1 -- ds50010--------
rs1425793401,2
--55207600(+) ATTGCA/GTTAGC 1 -- ds50010--------
rs1509278121,2
C--55207605(+) GTTAGC/TGAATG 1 -- ds50010--------
rs1861941291,2
C--55207652(+) CTTTGC/TGTAGT 1 -- ds50010--------
rs1498387571,2
--55207689(+) GATGAC/GTGTAA 1 -- ds50010--------
rs1468804761,2
--55207767(+) GAGAGA/GAGTTG 1 -- ds50010--------
rs1132388981,2
C--55207805(+) TATGCG/AATTGC 1 -- ds50011Minor allele frequency- A:0.00CSA 1

HapMap Linkage Disequilibrium report for MTRNR2L10 (55207824 - 55208944 bp)

Structural Variations
     Database of Genomic Variants (DGV) 3 variations for MTRNR2L10:    About this table    
Variant IDTypeSubtypePubMed ID
esv2740175CNV Deletion23290073
nsv435891CNV Deletion17901297
esv2740181CNV Deletion23290073

Site Specific Mutation Identification with PCR Assays
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(in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
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1 disease for MTRNR2L10:    
About MalaCards
alzheimer's disease


Find genes that share disorders with MTRNR2L10           About GenesLikeMe


Export disorders for MTRNR2L10 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 MTRNR2L10 gene integrated from 10 sources:
(articles sorted by number of sources associating them with MTRNR2L10)
    Utopia: connect your pdf to the dynamic
world of online information

  1. Evidence for potential functionality of nuclearly-encoded humanin isoforms. (PubMed id 19477263)1, 2, 3 Bodzioch M....Dembinska-Kiec A. (Genomics 2009)
  2. The DNA sequence of the human X chromosome. (PubMed id 15772651)1, 2 Ross M.T.... Bentley D.R. (Nature 2005)
  3. Humanin: a harbinger of mitochondrial-derived peptides? (PubMed id 23402768)1 Lee C....Cohen P. (Trends Endocrinol. Metab. 2013)
  4. Immunolocalization of humanin in human sperm and testis. (PubMed id 20542501)1 Moretti E....Collodel G. (Fertil. Steril. 2010)
  5. Humanin: a novel central regulator of peripheral insulin action. (PubMed id 19623253)1 Muzumdar R.H....Cohen P. (PLoS ONE 2009)
  6. Humanin peptide suppresses apoptosis by interfering with Bax activation. (PubMed id 12732850)1 Guo B....Reed J.C. (Nature 2003)
  7. Evidence for in vivo production of Humanin peptide, a neuroprotective factor against Alzheimer's disease-related insults. (PubMed id 12009529)1 Tajima H.... Nishimoto I. (Neurosci. Lett. 2002)
  8. A rescue factor abolishing neuronal cell death by a wide spectrum of familial Alzheimer's disease genes and Abeta. (PubMed id 11371646)1 Hashimoto Y.... Nashimoto I. (Proc. Natl. Acad. Sci. U.S.A. 2001)

(in PubMed, OMIM, and NCBI Bookshelf)
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 ANDOR
Aliases
Free Text  

  Query String
PubMed
OMIM
NCBI Bookshelf
  (Note: In FireFox, select the above section and copy using Ctrl-C)

(According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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Entrez Gene: 100463488 HGNC: 37167 Ensembl:ENSG00000256045 euGenes: HUgn100463488 ECgene: MTRNR2L10
H-InvDB: MTRNR2L10

(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 MTRNR2L10 Pharmacogenomics, SNPs, Pathways

(Patent information from GeneIP,
Licensable technologies from WIS Yeda, Salk, Tufts,
IP news from LifeMap Sciences, Inc.)
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Patent Information for MTRNR2L10 gene:
Search GeneIP for patents involving MTRNR2L10

GeneCards and IP:
Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



(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, eBioscience, and/or others, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Addgene, Cell lines from GenScript, and ESI BIO, Flow cytometery from eBioscience, 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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The GeneCards human gene database gene index: 1 3 5 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 


Developed at the Crown Human Genome Center, Department of Molecular Genetics, the Weizmann Institute of Science

Hot genes      Disease genes      MTRNR2L10 gene at Home site.
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