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Q8N3F9 (G137C_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 3, 2013. Version 55. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
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Names and origin

Protein namesRecommended name:
Integral membrane protein GPR137C
Alternative name(s):
Transmembrane 7 superfamily member 1-like 2 protein
Gene names
Name:GPR137C
Synonyms:TM7SF1L2
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length429 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Subcellular location

Membrane; Multi-pass membrane protein Potential.

Sequence similarities

Belongs to the GPR137 family.

Ontologies

Keywords
   Cellular componentMembrane
   Coding sequence diversityPolymorphism
   DomainTransmembrane
Transmembrane helix
   PTMGlycoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular_componentintegral to membrane

Inferred from electronic annotation. Source: UniProtKB-KW

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 429429Integral membrane protein GPR137C
PRO_0000304803

Regions

Topological domain1 – 4848Extracellular Potential
Transmembrane49 – 6921Helical; Potential
Topological domain70 – 8314Cytoplasmic Potential
Transmembrane84 – 10421Helical; Potential
Topological domain105 – 12016Extracellular Potential
Transmembrane121 – 14121Helical; Potential
Topological domain142 – 16726Cytoplasmic Potential
Transmembrane168 – 18821Helical; Potential
Topological domain189 – 20517Extracellular Potential
Transmembrane206 – 22621Helical; Potential
Topological domain227 – 24620Cytoplasmic Potential
Transmembrane247 – 26721Helical; Potential
Topological domain268 – 30033Extracellular Potential
Transmembrane301 – 32121Helical; Potential
Topological domain322 – 429108Cytoplasmic Potential

Amino acid modifications

Glycosylation2851N-linked (GlcNAc...) Potential

Natural variations

Natural variant2481V → I. Ref.3
Corresponds to variant rs762063 [ dbSNP | Ensembl ].
VAR_053880

Experimental info

Sequence conflict2391K → KITGSHSFLWLNSTPLC in CAD39035. Ref.3

Sequences

Sequence LengthMass (Da)Tools
Q8N3F9 [UniParc].

Last modified September 11, 2007. Version 2.
Checksum: DD307DE80AF6B1C8

FASTA42947,075
        10         20         30         40         50         60 
MRVSVPGPAA AAAPAAGREP STPGGGSGGG GAVAAASGAA VPGSVQLALS VLHALLYAAL 

        70         80         90        100        110        120 
FAFAYLQLWR LLLYRERRLS YQSLCLFLCL LWAALRTTLF SAAFSLSGSL PLLRPPAHLH 

       130        140        150        160        170        180 
FFPHWLLYCF PSCLQFSTLC LLNLYLAEVI CKVRCATELD RHKILLHLGF IMASLLFLVV 

       190        200        210        220        230        240 
NLTCAMLVHG DVPENQLKWT VFVRALINDS LFILCAISLV CYICKITKMS SANVYLESKG 

       250        260        270        280        290        300 
MSLCQTVVVG SVVILLYSSR ACYNLVVVTI SQDTLESPFN YGWDNLSDKA HVEDISGEEY 

       310        320        330        340        350        360 
IVFGMVLFLW EHVPAWSVVL FFRAQRLNQN LAPAGMINSH SYSSRAYFFD NPRRYDSDDD 

       370        380        390        400        410        420 
LPRLGSSREG SLPNSQSLGW YGTMTGCGSS SYTVTPHLNG PMTDTAPLLF TCSNLDLNNH 


HSLYVTPQN 

« Hide

References

[1]"The DNA sequence and analysis of human chromosome 14."
Heilig R., Eckenberg R., Petit J.-L., Fonknechten N., Da Silva C., Cattolico L., Levy M., Barbe V., De Berardinis V., Ureta-Vidal A., Pelletier E., Vico V., Anthouard V., Rowen L., Madan A., Qin S., Sun H., Du H. expand/collapse author list , Pepin K., Artiguenave F., Robert C., Cruaud C., Bruels T., Jaillon O., Friedlander L., Samson G., Brottier P., Cure S., Segurens B., Aniere F., Samain S., Crespeau H., Abbasi N., Aiach N., Boscus D., Dickhoff R., Dors M., Dubois I., Friedman C., Gouyvenoux M., James R., Madan A., Mairey-Estrada B., Mangenot S., Martins N., Menard M., Oztas S., Ratcliffe A., Shaffer T., Trask B., Vacherie B., Bellemere C., Belser C., Besnard-Gonnet M., Bartol-Mavel D., Boutard M., Briez-Silla S., Combette S., Dufosse-Laurent V., Ferron C., Lechaplais C., Louesse C., Muselet D., Magdelenat G., Pateau E., Petit E., Sirvain-Trukniewicz P., Trybou A., Vega-Czarny N., Bataille E., Bluet E., Bordelais I., Dubois M., Dumont C., Guerin T., Haffray S., Hammadi R., Muanga J., Pellouin V., Robert D., Wunderle E., Gauguet G., Roy A., Sainte-Marthe L., Verdier J., Verdier-Discala C., Hillier L.W., Fulton L., McPherson J., Matsuda F., Wilson R., Scarpelli C., Gyapay G., Wincker P., Saurin W., Quetier F., Waterston R., Hood L., Weissenbach J.
Nature 421:601-607(2003) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[2]"The G protein-coupled receptor repertoires of human and mouse."
Vassilatis D.K., Hohmann J.G., Zeng H., Li F., Ranchalis J.E., Mortrud M.T., Brown A., Rodriguez S.S., Weller J.R., Wright A.C., Bergmann J.E., Gaitanaris G.A.
Proc. Natl. Acad. Sci. U.S.A. 100:4903-4908(2003) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 32-148.
[3]"The full-ORF clone resource of the German cDNA consortium."
Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H., Heubner D., Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A., Wiemann S., Schupp I.
BMC Genomics 8:399-399(2007) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 48-429, VARIANT ILE-248.
Tissue: Melanoma.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL157971 Genomic DNA. No translation available.
AY255590 mRNA. Translation: AAO85102.1.
AL834372 mRNA. Translation: CAD39035.1.
IPIIPI00855960.
RefSeqNP_001093122.1. NM_001099652.1.
UniGeneHs.416214.

3D structure databases

ProteinModelPortalQ8N3F9.
ModBaseSearch...

Protein-protein interaction databases

STRING9606.ENSP00000315106.

Polymorphism databases

DMDM158563844.

Proteomic databases

PaxDbQ8N3F9.
PRIDEQ8N3F9.

Protocols and materials databases

DNASU283554.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000321662; ENSP00000315106; ENSG00000180998.
GeneID283554.
KEGGhsa:283554.
UCSCuc001wzt.4. human.

Organism-specific databases

CTD283554.
GeneCardsGC14P053020.
H-InvDBHIX0011659.
HGNCHGNC:25445. GPR137C.
HPAHPA030763.
neXtProtNX_Q8N3F9.
PharmGKBPA143485483.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG307093.
HOGENOMHOG000286020.
HOVERGENHBG058911.
InParanoidQ8N3F9.
OMALSDKAHV.
OrthoDBEOG4H9XKT.

Gene expression databases

ArrayExpressQ8N3F9.
BgeeQ8N3F9.
CleanExHS_GPR137C.
GenevestigatorQ8N3F9.

Family and domain databases

ProtoNetSearch...

Other

GenomeRNAi283554.
NextBio94034.

Entry information

Entry nameG137C_HUMAN
AccessionPrimary (citable) accession number: Q8N3F9
Secondary accession number(s): Q86SM2
Entry history
Integrated into UniProtKB/Swiss-Prot: September 11, 2007
Last sequence update: September 11, 2007
Last modified: April 3, 2013
This is version 55 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 14

Human chromosome 14: 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