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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

NMS Gene

protein-coding   GIFtS: 44
GCID: GC02P101086

neuromedin S

 Explore 9 diseases affiliated with
NMS via our new
 Human Malady Compendium 
Biological research products
for NMS
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Neuromedin S1 2
Neuromedin-S1
BCS1L5
BJS5
FLGRACILE5
PTD5

External Ids:    HGNC: 322031   Entrez Gene: 1295212   Ensembl: ENSG000002046407   OMIM: 6036475   UniProtKB: Q5H8A33   

Export aliases for NMS gene to outside databases

Previous GC identifers: GC02P100546 GC02P100453 GC02P094851


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

UniProtKB/Swiss-Prot: NMS_HUMAN, Q5H8A3
Function: Implicated in the regulation of circadian rhythms through autocrine and/or paracrine actions (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 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000002.11  NC_018913.1  NT_022171.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the NMS gene promoter:
         STAT1   AML1a   NRSF form 1   NF-YC   CUTL1   Nkx2-5   Cdc5   NRSF form 2   Evi-1   IRF-2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidNMS promoter sequence
   Search SABiosciences Chromatin IP Primers for NMS

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat NMS


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

Entrez Gene cytogenetic band: 2q11.2   Ensembl cytogenetic band:  2q11.2   HGNC cytogenetic band: 2q11.2

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

GeneLoc information about chromosome 2         GeneLoc Exon Structure

GeneLoc location for GC02P101086:  view genomic region     (about GC identifiers)

Start:
101,086,944 bp from pter      End:
101,099,742 bp from pter
Size:
12,799 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, 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 Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: NMS_HUMAN, Q5H8A3 (See protein sequence)
Recommended Name: Neuromedin-S precursor  
Size: 153 amino acids; 17731 Da
Subcellular location: Secreted (By similarity)

Explore the universe of human proteins at neXtProt for NMS: NX_Q5H8A3

NMS Protein expression data from MOPED and PaxDb:    About this image 

Estimated protein expression log10 (pmol).

REFSEQ proteins: NP_001011717.1  
ENSEMBL proteins: 
 ENSP00000366061  
Reactome Protein details: Q5H8A3
Human Recombinant Protein Products: 
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Uscn Proteins for NMS

Gene Ontology (GO): 1 cellular component term (GO ID links to tree view):    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0005576extracellular region TAS--


NMS for ontologies           About GeneDecksing



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(According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
About This Section

NMS for domains           About GeneDecksing

2 InterPro domains/families:
 IPR018070 Neuromedin-U_amidation-site
 IPR008200 NMU_C

Graphical View of Domain Structure for InterPro Entry Q5H8A3

ProtoNet protein and cluster: Q5H8A3

UniProtKB/Swiss-Prot: NMS_HUMAN, Q5H8A3
Similarity: Belongs to the NmU family


(According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
About This Section

Function Summary:

     UniProtKB/Swiss-Prot: NMS_HUMAN, Q5H8A3
Function: Implicated in the regulation of circadian rhythms through autocrine and/or paracrine actions (By similarity)

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In Situ Assay
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Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for NMS

Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0001664G-protein coupled receptor binding ----


NMS for ontologies           About GeneDecksing



(Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, 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 Mar 2013 via Entrez Gene).
About This Section

Unified GeneCards pathways  About this table 
See pathways by source

Super-pathwaycontained gene-specific pathways
1Class A/1 (Rhodopsin-like receptors)
Class A/1 (Rhodopsin-like receptors)1.00
Peptide ligand-binding receptors0.61
GPCR ligand binding0.75
G alpha (i) signalling events0.44
2Signaling by GPCR
Signaling by GPCR1.00
Signal Transduction0.56
GPCR downstream signaling0.89
3G alpha (q) signalling events
G alpha (q) signalling events1.00
Gastrin-CREB signalling pathway via PKC and MAPK0.90

Pathway sources
See GeneCards unified pathways
Show all pathways


5/9        Reactome Pathways for NMS (see all 9)
    GPCR downstream signaling
Peptide ligand-binding receptors
Gastrin-CREB signalling pathway via PKC and MAPK
Signaling by GPCR
GPCR ligand binding



NMS for pathways           About GeneDecksing

Interactions:

    Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for NMS

STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

5/247 Interacting proteins for NMS (Q5H8A33 ENSP000003660614) via UniProtKB, MINT, STRING, and/or I2D (see all 247)
InteractantInteraction Details
GeneCardExternal ID(s)
NMUR1Q9HB893, ENSP000003058774I2D: score=3 STRING: ENSP00000305877
NMUR2Q9GZQ43, ENSP000002552624I2D: score=2 STRING: ENSP00000255262
CASRENSP000002961544STRING: ENSP00000296154
CCKENSP000003356574STRING: ENSP00000335657
DRD2ENSP000003548594STRING: ENSP00000354859
About this table

Gene Ontology (GO): 3 biological process terms (GO ID links to tree view):    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0006940regulation of smooth muscle contraction IEA--
GO:0007218neuropeptide signaling pathway IEA--
GO:0045475locomotor rhythm ----


NMS for ontologies           About GeneDecksing



(Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
About This Section
Browse Small Molecules at EMD Millipore
Browse drugs & compounds from Enzo Life Sciences

Browse Tocris compounds for NMS
Search CenterWatch for drugs/clinical trials and news about NMS 

(Secondary structures according to fRNAdb,
GenBank/EMBL/DDBJ Accessions according to
Unigene (Build 235 Homo sapiens; Mar 10 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,
RNAi Products from EMD Millipore,
siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
About This Section

REFSEQ mRNAs for NMS gene: 
NM_001011717.1  

Unigene Cluster for NMS:

Neuromedin S
Hs.567676
Unigene Representative Sequence: AB164464
1 Ensembl transcript including schematic representation, and UCSC links where relevant:
ENST00000376865(uc002tan.1)

miRNA
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Inhib. RNA
Products:
     
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OriGene siRNA: NMS
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Clone
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  QIAGEN QuantiFast Probe-based Assays in human, mouse, rat NMS

Additional cDNA sequence: AB164464.1 

1 DOTS entry:

DT.120994010 

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™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
About This Section

NMS expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: CTACAGATTC

Microarray
RNAseq (Illumina Body Map)
(100×FPKM)½
SAGE (Serial Analysis of Gene Expression)

About this image
See NMS Protein Expression from SPIRE MOPED and PaxDB
SOURCE GeneReport for Unigene cluster: Hs.567676
    SABiosciences Expression via Pathway-Focused PCR Array including NMS: 
          Circadian Rhythms in human mouse rat

Primer
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In Situ
Assay Products:
 

 
Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for NMS

(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)
About This Section

This gene was present in the common ancestor of chordates.

Orthologs for NMS gene from 3/7 species (see all 7)    About this table
Organism Taxonomic
classification
Gene Description Human
Similarity
Orthology
Type
Details
mouse
(Mus musculus)
Mammalia Nms1 , 5 neuromedin S1, 5 76.44(n)1
66(a)1
  1 (17.31 cM)5
4332921  NM_001011684.21  NP_001011684.31 
 389391495 
chicken
(Gallus gallus)
Aves --
Uncharacterized protein
36(a)
1 ↔ 1
1(137269821-137274811)
zebrafish
(Danio rerio)
Actinopterygii BC057408.12   -- 73.69(n)   393603  BC057408.1 


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

(Paralogs according to 1HomoloGene,
2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
About This Section
  --

(SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, 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) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
About This Section

10/307 NCBI SNPs in NMS are shown (see all 307    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 2 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs803477461,2
F,--101084947(+) TGCATA/GAACAC 1 -- us2k11Minor allele frequency- G:0.04WA 118
rs75993211,2
C,F,A,H,--101085113(+) AAAAAT/GCATTT 1 -- us2k110Minor allele frequency- G:0.29NS EA NA WA 780
rs1998270111,2
--101085125(+) TCATG-/TTTTTT 1 -- us2k10--------
rs1424485121,2
--101085254(+) ACTGTA/TATAAA 1 -- us2k10--------
rs76087741,2
C,F,A,H,--101085322(+) GTAGTG/TTATAA 1 -- us2k18Minor allele frequency- T:0.28NS NA WA EA 478
rs75995571,2
C,F,A,--101085332(+) ATTATT/CGCTCT 1 -- us2k16Minor allele frequency- C:0.29NA WA EA 364
rs75995651,2
C,F,A,--101085339(+) CTCTGT/CTATGA 1 -- us2k16Minor allele frequency- C:0.29NA WA EA 364
rs75968511,2
C,F,H,--101085481(+) TATTAA/GCATGT 1 -- us2k1 tfbs38Minor allele frequency- G:0.28NS EA WA NA 774
rs1468521331,2
--101085483(+) TTAACA/GTGTTT 1 -- us2k10--------
rs46307911,2
C,F,A,H,--101085556(+) AAAGAC/TATGCG 1 -- us2k1 tfbs310Minor allele frequency- T:0.29NS EA NA WA 782

HapMap Linkage Disequilibrium report for NMS (101086944 - 101099742 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
Database of Genomic Variants (DGV): 1 variation for NMS
     1 CNV: 4302

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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.)
About This Section

NMS for disorders           About GeneDecksing

OMIM gene information: 603647   
OMIM disorders: 124000  603358  256000  262000  
9 diseases for NMS:    About MalaCards
acral lentiginous melanoma    mitochondrial complex iii deficiency    neuroleptic malignant syndrome    bjornstad syndrome
gracile syndrome    nodular malignant melanoma    anorexia nervosa    thymoma
melanoma

Human Genome Epidemiology (HuGE) Navigator: NMS (10 documents)

Export disorders for NMS 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)
About This Section

PubMed articles for NMS gene integrated from 9 sources:
(articles sorted by number of sources associating them with NMS)
    Utopia: connect your pdf to the dynamic
world of online information

  1. Identification of neuromedin S and its possible role in the mammalian circadian oscillator system. (PubMed id 15635449)1, 2, 3 Mori K.... Kangawa K. (2005)
  2. Expression and vasoconstrictor function of anorexigenic peptides neuromedin U-25 and S in the human cardiovascular system. (PubMed id 18987052)1, 9 Mitchell J.D....Davenport A.P. (2009)
  3. Emerging pharmacology and physiology of neuromedin U and the structurally related peptide neuromedin S. (PubMed id 19519756)1, 9 Mitchell J.D....Davenport A.P. (2009)
  4. Association study of 182 candidate genes in anorexia nervosa. (PubMed id 20468064)1 Pinheiro A.P....Woodside D.B. (2010)
  5. Identification and functional analysis of a novel ligand for G protein-coupled receptor, Neuromedin S. (PubMed id 17870195)1 Miyazato M....Kangawa K. (2008)
  6. Stable association between G alpha(q) and phospholipase C beta 1 in living cells. (PubMed id 16754659)1 Dowal L....Scarlata S. (2006)
  7. Identification and characterization of two neuromedin U receptors differentially expressed in peripheral tissues and the central nervous system. (PubMed id 10899166)1 Raddatz R....Adham N. (2000)
  8. Expression of NMS and NMU2R in the pig reproductive a xis during the estrus cycle and the effect of NMS on the reproductive axis in v itro. (PubMed id 19781586)9 Yang G....Liu Y. (2009)
  9. Structural and functional analogs of the novel mammalian neuropeptide, neuromedin S (NmS), in the dermal venoms of Eurasian bombinid toads. (PubMed id 16682011)9 Chen T....Shaw C. (2006)
  10. Appetite-modifying actions of pro-neuromedin U-derive d peptides. (PubMed id 19531638)9 Bechtold D.A....Luckman S.M. (2009)

(in PubMed, OMIM, and NCBI Bookshelf)
About This Section
 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)
About This Section
Entrez Gene: 129521 HGNC: 32203 Ensembl:ENSG00000204640 euGenes: HUgn129521 ECgene: NMS
H-InvDB: NMS

(According to HUGE)
About This Section
  --

(According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
About This Section
NameDescription
PharmGKB entry for NMS Pharmacogenomics, SNPs, Pathways

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

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, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
In Situ Hybridization Assays from
Advanced Cell Diagnostics
About This Section

 
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 QIAGEN Custom miScript Target Protector blocks miRNA-binding site of in human, mouse, rat NMS
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GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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VWF
(GIFTS: 73)
von Willebrand factor
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The GeneCards human gene database gene index: 1 3 5 6 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 


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