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O95897 (NOE2_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 87. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Noelin-2
Alternative name(s):
Olfactomedin-2
Gene names
Name:OLFM2
Synonyms:NOE2
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length454 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at transcript level

General annotation (Comments)

Subcellular location

Secreted Probable.

Sequence similarities

Contains 1 olfactomedin-like domain.

Ontologies

Keywords
   Cellular componentSecreted
   Coding sequence diversityPolymorphism
   DomainCoiled coil
Signal
   PTMDisulfide bond
Glycoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular componentextracellular region

Inferred from electronic annotation. Source: UniProtKB-SubCell

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 2020 Potential
Chain21 – 454434Noelin-2
PRO_0000020078

Regions

Domain194 – 446253Olfactomedin-like
Coiled coil58 – 8528 Potential
Coiled coil136 – 19358 Potential

Amino acid modifications

Glycosylation741N-linked (GlcNAc...) Potential
Glycosylation1551N-linked (GlcNAc...) Potential
Glycosylation2751N-linked (GlcNAc...) Potential
Glycosylation3101N-linked (GlcNAc...) Potential
Glycosylation3991N-linked (GlcNAc...) Potential
Glycosylation4411N-linked (GlcNAc...) Potential
Disulfide bond195 ↔ 377 By similarity

Natural variations

Natural variant861T → M in a colorectal cancer sample; somatic mutation. Ref.5
VAR_036532
Natural variant1061R → Q. Ref.1
Corresponds to variant rs2303100 [ dbSNP | Ensembl ].
VAR_022550
Natural variant1271T → M. Ref.1
Corresponds to variant rs11556087 [ dbSNP | Ensembl ].
VAR_050423

Sequences

Sequence LengthMass (Da)Tools
O95897 [UniParc].

Last modified June 7, 2005. Version 2.
Checksum: EBF4AE8DF909C77F

FASTA45451,386
        10         20         30         40         50         60 
MWPLTVPPPL LLLLCSGLAG QTLFQNPEEG WQLYTSAQAP DGKCICTAVI PAQSTCSRDG 

        70         80         90        100        110        120 
RSRELRQLME KVQNVSQSME VLELRTYRDL QYVRGMETLM RSLDARLRAA DGSLSAKSFQ 

       130        140        150        160        170        180 
ELKDRMTELL PLSSVLEQYK ADTRTIVRLR EEVRNLSGSL AAIQEEMGAY GYEDLQQRVM 

       190        200        210        220        230        240 
ALEARLHACA QKLGCGKLTG VSNPITVRAM GSRFGSWMTD TMAPSADSRV WYMDGYYKGR 

       250        260        270        280        290        300 
RVLEFRTLGD FIKGQNFIQH LLPQPWAGTG HVVYNGSLFY NKYQSNVVVK YHFRSRSVLV 

       310        320        330        340        350        360 
QRSLPGAGYN NTFPYSWGGF SDMDFMVDES GLWAVYTTNQ NAGNIVVSRL DPHTLEVMRS 

       370        380        390        400        410        420 
WDTGYPKRSA GEAFMICGVL YVTNSHLAGA KVYFAYFTNT SSYEYTDVPF HNQYSHISML 

       430        440        450 
DYNPRERALY TWNNGHQVLY NVTLFHVIST SGDP 

« Hide

References

« Hide 'large scale' references
[1]Mei G., Yu W., Gibbs R.A.
Submitted (FEB-1999) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANTS GLN-106 AND MET-127.
Tissue: Brain.
[2]"The DNA sequence and biology of human chromosome 19."
Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E., Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M., Aerts A., Altherr M., Ashworth L., Bajorek E., Black S., Branscomb E., Caenepeel S., Carrano A.V. expand/collapse author list , Caoile C., Chan Y.M., Christensen M., Cleland C.A., Copeland A., Dalin E., Dehal P., Denys M., Detter J.C., Escobar J., Flowers D., Fotopulos D., Garcia C., Georgescu A.M., Glavina T., Gomez M., Gonzales E., Groza M., Hammon N., Hawkins T., Haydu L., Ho I., Huang W., Israni S., Jett J., Kadner K., Kimball H., Kobayashi A., Larionov V., Leem S.-H., Lopez F., Lou Y., Lowry S., Malfatti S., Martinez D., McCready P.M., Medina C., Morgan J., Nelson K., Nolan M., Ovcharenko I., Pitluck S., Pollard M., Popkie A.P., Predki P., Quan G., Ramirez L., Rash S., Retterer J., Rodriguez A., Rogers S., Salamov A., Salazar A., She X., Smith D., Slezak T., Solovyev V., Thayer N., Tice H., Tsai M., Ustaszewska A., Vo N., Wagner M., Wheeler J., Wu K., Xie G., Yang J., Dubchak I., Furey T.S., DeJong P., Dickson M., Gordon D., Eichler E.E., Pennacchio L.A., Richardson P., Stubbs L., Rokhsar D.S., Myers R.M., Rubin E.M., Lucas S.M.
Nature 428:529-535(2004) [PubMed: 15057824] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Brain.
[4]"Bioinformatic approaches for identification and characterization of olfactomedin related genes with a potential role in pathogenesis of ocular disorders."
Mukhopadhyay A., Talukdar S., Bhattacharjee A., Ray K.
Mol. Vis. 10:304-314(2004) [PubMed: 15123989] [Abstract]
Cited for: IDENTIFICATION OF GENOMIC DNA.
[5]"The consensus coding sequences of human breast and colorectal cancers."
Sjoeblom T., Jones S., Wood L.D., Parsons D.W., Lin J., Barber T.D., Mandelker D., Leary R.J., Ptak J., Silliman N., Szabo S., Buckhaults P., Farrell C., Meeh P., Markowitz S.D., Willis J., Dawson D., Willson J.K.V. expand/collapse author list , Gazdar A.F., Hartigan J., Wu L., Liu C., Parmigiani G., Park B.H., Bachman K.E., Papadopoulos N., Vogelstein B., Kinzler K.W., Velculescu V.E.
Science 314:268-274(2006) [PubMed: 16959974] [Abstract]
Cited for: VARIANT [LARGE SCALE ANALYSIS] MET-86.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF131839 mRNA. Translation: AAD20056.1.
AC008742 Genomic DNA. No translation available.
BC011361 mRNA. Translation: AAH11361.1.
BK001428 Genomic DNA. Translation: DAA01550.1.
IPIIPI00295767.
RefSeqNP_477512.1. NM_058164.2.
UniGeneHs.169743.

3D structure databases

ProteinModelPortalO95897.
ModBaseSearch...

Protein-protein interaction databases

IntActO95897. 11 interactions.
MINTMINT-1385503.
STRINGO95897.

Proteomic databases

PRIDEO95897.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000264833; ENSP00000264833; ENSG00000105088.
GeneID93145.
KEGGhsa:93145.
UCSCuc002mmo.1. human.

Organism-specific databases

CTD93145.
GeneCardsGC19M009964.
HGNCHGNC:17189. OLFM2.
neXtProtNX_O95897.
PharmGKBPA31916.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG13587.
GeneTreeENSGT00560000076789.
HOGENOMHBG717166.
HOVERGENHBG006513.
InParanoidO95897.
OMAWPLTVPP.
OrthoDBEOG4QZ7KQ.
PhylomeDBO95897.

Gene expression databases

ArrayExpressO95897.
BgeeO95897.
CleanExHS_OLFM2.
GenevestigatorO95897.
GermOnlineENSG00000105088. Homo sapiens.

Family and domain databases

InterProIPR022082. Noelin-1.
IPR003112. Olfac-like.
[Graphical view]
PfamPF12308. Noelin-1. 1 hit.
PF02191. OLF. 1 hit.
[Graphical view]
SMARTSM00284. OLF. 1 hit.
[Graphical view]
PROSITEPS51132. OLF. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio78006.

Entry information

Entry nameNOE2_HUMAN
AccessionPrimary (citable) accession number: O95897
Secondary accession number(s): Q6IMJ3, Q96FC2
Entry history
Integrated into UniProtKB/Swiss-Prot: February 21, 2001
Last sequence update: June 7, 2005
Last modified: January 25, 2012
This is version 87 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 19

Human chromosome 19: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

SIMILARITY comments

Index of protein domains and families