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P0C862

- C1T9A_HUMAN

UniProt

P0C862 - C1T9A_HUMAN

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Protein
Complement C1q and tumor necrosis factor-related protein 9A
Gene
C1QTNF9, C1QTNF9A, UNQ6503/PRO21380
Organism
Homo sapiens (Human)
Status
Reviewed - Annotation score: 3 out of 5 - Experimental evidence at protein leveli

Functioni

Probable adipokine. Activates AMPK, AKT, and p44/42 MAPK signaling pathways By similarity.

Keywords - Molecular functioni

Hormone

Names & Taxonomyi

Protein namesi
Recommended name:
Complement C1q and tumor necrosis factor-related protein 9A
Alternative name(s):
Complement C1q and tumor necrosis factor-related protein 9
Gene namesi
Name:C1QTNF9
Synonyms:C1QTNF9A
ORF Names:UNQ6503/PRO21380
OrganismiHomo sapiens (Human)
Taxonomic identifieri9606 [NCBI]
Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
ProteomesiUP000005640: Chromosome 13

Organism-specific databases

HGNCiHGNC:28732. C1QTNF9.

Subcellular locationi

Secreted By similarity 1 Publication

GO - Cellular componenti

  1. collagen trimer Source: UniProtKB-KW
  2. extracellular region Source: UniProtKB-SubCell
Complete GO annotation...

Keywords - Cellular componenti

Secreted

Pathology & Biotechi

Organism-specific databases

PharmGKBiPA145008937.

PTM / Processingi

Molecule processing

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Signal peptidei1 – 1919 Reviewed prediction
Add
BLAST
Chaini20 – 333314Complement C1q and tumor necrosis factor-related protein 9A
PRO_0000291751Add
BLAST

Amino acid modifications

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Modified residuei31 – 3114-hydroxyproline By similarity
Modified residuei34 – 3414-hydroxyproline By similarity
Modified residuei40 – 4014-hydroxyproline By similarity
Modified residuei58 – 5814-hydroxyproline By similarity
Modified residuei61 – 6114-hydroxyproline By similarity
Modified residuei64 – 6414-hydroxyproline By similarity
Modified residuei73 – 7315-hydroxylysine By similarity
Glycosylationi73 – 731O-linked (Gal...) By similarity
Modified residuei127 – 12715-hydroxylysine By similarity
Glycosylationi127 – 1271O-linked (Gal...) By similarity
Modified residuei151 – 15114-hydroxyproline By similarity
Modified residuei160 – 16014-hydroxyproline By similarity
Modified residuei175 – 17514-hydroxyproline By similarity

Keywords - PTMi

Glycoprotein, Hydroxylation

Proteomic databases

PaxDbiP0C862.
PRIDEiP0C862.

Expressioni

Tissue specificityi

Expressed predominantly in adipose tissue.1 Publication

Gene expression databases

BgeeiP0C862.
CleanExiHS_C1QTNF9.
GenevestigatoriP0C862.

Interactioni

Subunit structurei

Multimers (predominantly trimers). Interacts with ADIPOQ via the C1q domain to form a heterotrimeric complex By similarity. Interacts with CTRP9B. Forms heterotrimers and heterooligomeric complexes with CTRP9B.1 Publication

Protein-protein interaction databases

IntActiP0C862. 17 interactions.

Structurei

3D structure databases

ProteinModelPortaliP0C862.
SMRiP0C862. Positions 201-330.

Family & Domainsi

Domains and Repeats

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Domaini24 – 8259Collagen-like 1
Add
BLAST
Domaini95 – 15460Collagen-like 2
Add
BLAST
Domaini155 – 19137Collagen-like 3
Add
BLAST
Domaini197 – 333137C1q
Add
BLAST

Sequence similaritiesi

Contains 1 C1q domain.

Keywords - Domaini

Collagen, Repeat, Signal

Phylogenomic databases

eggNOGiNOG12793.
HOGENOMiHOG000085653.
HOVERGENiHBG108220.
InParanoidiP0C862.
OMAiCYLEINC.
OrthoDBiEOG70ZZPW.
PhylomeDBiP0C862.
TreeFamiTF334029.

Family and domain databases

Gene3Di2.60.120.40. 1 hit.
InterProiIPR001073. C1q.
IPR008160. Collagen.
IPR008983. Tumour_necrosis_fac-like_dom.
[Graphical view]
PfamiPF00386. C1q. 1 hit.
PF01391. Collagen. 3 hits.
[Graphical view]
PRINTSiPR00007. COMPLEMNTC1Q.
SMARTiSM00110. C1Q. 1 hit.
[Graphical view]
SUPFAMiSSF49842. SSF49842. 1 hit.
PROSITEiPS50871. C1Q. 1 hit.
[Graphical view]

Sequencei

Sequence statusi: Complete.

Sequence processingi: The displayed sequence is further processed into a mature form.

P0C862-1 [UniParc]FASTAAdd to Basket

« Hide

MRIWWLLLAI EICTGNINSQ DTCRQGHPGI PGNPGHNGLP GRDGRDGAKG    50
DKGDAGEPGR PGSPGKDGTS GEKGERGADG KVEAKGIKGD QGSRGSPGKH 100
GPKGLAGPMG EKGLRGETGP QGQKGNKGDV GPTGPEGPRG NIGPLGPTGL 150
PGPMGPIGKP GPKGEAGPTG PQGEPGVRGI RGWKGDRGEK GKIGETLVLP 200
KSAFTVGLTV LSKFPSSDMP IKFDKILYNE FNHYDTAAGK FTCHIAGVYY 250
FTYHITVFSR NVQVSLVKNG VKILHTKDAY MSSEDQASGG IVLQLKLGDE 300
VWLQVTGGER FNGLFADEDD DTTFTGFLLF SSP 333
Length:333
Mass (Da):34,681
Last modified:September 2, 2008 - v1
Checksum:iF2EBF303B034E307
GO

Natural variant

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Natural varianti6 – 61L → F.
Corresponds to variant rs1974332 [ dbSNP | Ensembl ].
VAR_059148
Natural varianti219 – 2191M → V.3 Publications
Corresponds to variant rs3751357 [ dbSNP | Ensembl ].
VAR_032840
Natural varianti301 – 3011V → M.1 Publication
Corresponds to variant rs4589405 [ dbSNP | Ensembl ].
VAR_032841

Sequence databases

Select the link destinations:
EMBL
GenBank
DDBJ
Links Updated
AY358145 mRNA. Translation: AAQ88512.1.
AL359736 Genomic DNA. Translation: CAH72292.1.
AL359736 Genomic DNA. Translation: CAH72293.1.
BC040438 mRNA. Translation: AAH40438.1.
CCDSiCCDS9306.1.
RefSeqiNP_848635.2. NM_178540.3.
UniGeneiHs.362854.

Genome annotation databases

EnsembliENST00000332018; ENSP00000333737; ENSG00000240654.
ENST00000382071; ENSP00000371503; ENSG00000240654.
GeneIDi338872.
KEGGihsa:338872.
UCSCiuc001upj.3. human.

Polymorphism databases

DMDMi205686199.

Keywords - Coding sequence diversityi

Polymorphism

Cross-referencesi

Sequence databases

Select the link destinations:
EMBL
GenBank
DDBJ
Links Updated
AY358145 mRNA. Translation: AAQ88512.1 .
AL359736 Genomic DNA. Translation: CAH72292.1 .
AL359736 Genomic DNA. Translation: CAH72293.1 .
BC040438 mRNA. Translation: AAH40438.1 .
CCDSi CCDS9306.1.
RefSeqi NP_848635.2. NM_178540.3.
UniGenei Hs.362854.

3D structure databases

ProteinModelPortali P0C862.
SMRi P0C862. Positions 201-330.
ModBasei Search...
MobiDBi Search...

Protein-protein interaction databases

IntActi P0C862. 17 interactions.

Polymorphism databases

DMDMi 205686199.

Proteomic databases

PaxDbi P0C862.
PRIDEi P0C862.

Protocols and materials databases

DNASUi 338872.
Structural Biology Knowledgebase Search...

Genome annotation databases

Ensembli ENST00000332018 ; ENSP00000333737 ; ENSG00000240654 .
ENST00000382071 ; ENSP00000371503 ; ENSG00000240654 .
GeneIDi 338872.
KEGGi hsa:338872.
UCSCi uc001upj.3. human.

Organism-specific databases

CTDi 338872.
GeneCardsi GC13P024881.
H-InvDB HIX0079546.
HGNCi HGNC:28732. C1QTNF9.
MIMi 614285. gene.
neXtProti NX_P0C862.
PharmGKBi PA145008937.
GenAtlasi Search...

Phylogenomic databases

eggNOGi NOG12793.
HOGENOMi HOG000085653.
HOVERGENi HBG108220.
InParanoidi P0C862.
OMAi CYLEINC.
OrthoDBi EOG70ZZPW.
PhylomeDBi P0C862.
TreeFami TF334029.

Miscellaneous databases

GenomeRNAii 338872.
NextBioi 97187.
PROi P0C862.
SOURCEi Search...

Gene expression databases

Bgeei P0C862.
CleanExi HS_C1QTNF9.
Genevestigatori P0C862.

Family and domain databases

Gene3Di 2.60.120.40. 1 hit.
InterProi IPR001073. C1q.
IPR008160. Collagen.
IPR008983. Tumour_necrosis_fac-like_dom.
[Graphical view ]
Pfami PF00386. C1q. 1 hit.
PF01391. Collagen. 3 hits.
[Graphical view ]
PRINTSi PR00007. COMPLEMNTC1Q.
SMARTi SM00110. C1Q. 1 hit.
[Graphical view ]
SUPFAMi SSF49842. SSF49842. 1 hit.
PROSITEi PS50871. C1Q. 1 hit.
[Graphical view ]
ProtoNeti Search...

Publicationsi

« Hide 'large scale' publications
  1. "CTRP8 and CTRP9B are novel proteins that hetero-oligomerize with C1q/TNF family members."
    Peterson J.M., Wei Z., Wong G.W.
    Biochem. Biophys. Res. Commun. 388:360-365(2009) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA], SUBCELLULAR LOCATION, INTERACTION WITH C1QL1, TISSUE SPECIFICITY.
    Tissue: Hippocampus.
  2. Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT VAL-219.
  3. "The DNA sequence and analysis of human chromosome 13."
    Dunham A., Matthews L.H., Burton J., Ashurst J.L., Howe K.L., Ashcroft K.J., Beare D.M., Burford D.C., Hunt S.E., Griffiths-Jones S., Jones M.C., Keenan S.J., Oliver K., Scott C.E., Ainscough R., Almeida J.P., Ambrose K.D., Andrews D.T.
    , Ashwell R.I.S., Babbage A.K., Bagguley C.L., Bailey J., Bannerjee R., Barlow K.F., Bates K., Beasley H., Bird C.P., Bray-Allen S., Brown A.J., Brown J.Y., Burrill W., Carder C., Carter N.P., Chapman J.C., Clamp M.E., Clark S.Y., Clarke G., Clee C.M., Clegg S.C., Cobley V., Collins J.E., Corby N., Coville G.J., Deloukas P., Dhami P., Dunham I., Dunn M., Earthrowl M.E., Ellington A.G., Faulkner L., Frankish A.G., Frankland J., French L., Garner P., Garnett J., Gilbert J.G.R., Gilson C.J., Ghori J., Grafham D.V., Gribble S.M., Griffiths C., Hall R.E., Hammond S., Harley J.L., Hart E.A., Heath P.D., Howden P.J., Huckle E.J., Hunt P.J., Hunt A.R., Johnson C., Johnson D., Kay M., Kimberley A.M., King A., Laird G.K., Langford C.J., Lawlor S., Leongamornlert D.A., Lloyd D.M., Lloyd C., Loveland J.E., Lovell J., Martin S., Mashreghi-Mohammadi M., McLaren S.J., McMurray A., Milne S., Moore M.J.F., Nickerson T., Palmer S.A., Pearce A.V., Peck A.I., Pelan S., Phillimore B., Porter K.M., Rice C.M., Searle S., Sehra H.K., Shownkeen R., Skuce C.D., Smith M., Steward C.A., Sycamore N., Tester J., Thomas D.W., Tracey A., Tromans A., Tubby B., Wall M., Wallis J.M., West A.P., Whitehead S.L., Willey D.L., Wilming L., Wray P.W., Wright M.W., Young L., Coulson A., Durbin R.M., Hubbard T., Sulston J.E., Beck S., Bentley D.R., Rogers J., Ross M.T.
    Nature 428:522-528(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], VARIANTS VAL-219 AND MET-301.
  4. "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] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT VAL-219.

Entry informationi

Entry nameiC1T9A_HUMAN
AccessioniPrimary (citable) accession number: P0C862
Secondary accession number(s): A2A3T6
, Q0VGC5, Q5VX65, Q5VX66, Q8IUU4
Entry historyi
Integrated into UniProtKB/Swiss-Prot: September 2, 2008
Last sequence update: September 2, 2008
Last modified: July 9, 2014
This is version 53 of the entry and version 1 of the sequence. [Complete history]
Entry statusiReviewed (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.

Miscellaneousi

Keywords - Technical termi

Complete proteome, Reference proteome

Documents

  1. Human chromosome 13
    Human chromosome 13: entries, gene names and cross-references to MIM
  2. Human entries with polymorphisms or disease mutations
    List of human entries with polymorphisms or disease mutations
  3. Human polymorphisms and disease mutations
    Index of human polymorphisms and disease mutations
  4. MIM cross-references
    Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot
  5. SIMILARITY comments
    Index of protein domains and families

External Data

Dasty 3

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