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A0PJX2 (CT118_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 38. 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:
Uncharacterized protein C20orf118
Gene names
Name:C20orf118
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length215 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Sequence similarities

Belongs to the OXR1 family.

Contains 1 TLD domain.

Ontologies

Keywords
   Coding sequence diversityPolymorphism
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
None. [Check GOA]

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 215215Uncharacterized protein C20orf118
PRO_0000318690

Regions

Domain79 – 215137TLD
Compositional bias26 – 327Poly-Glu

Natural variations

Natural variant1021G → R.
Corresponds to variant rs3748460 [ dbSNP | Ensembl ].
VAR_050439

Sequences

Sequence LengthMass (Da)Tools
A0PJX2 [UniParc].

Last modified January 9, 2007. Version 1.
Checksum: 6245E8FAC2C16D15

FASTA21523,912
        10         20         30         40         50         60 
MRGLRWRYTR LPSQVEDTLS GEEGNEEEEE EEAAPDPAAA PEDPTVPQLT EASQVLSASE 

        70         80         90        100        110        120 
IRQLSFHFPP RVTGHPWSLV FCTSRDGFSL QSLYRRMEGC SGPVLLVLRD QDGQIFGAFS 

       130        140        150        160        170        180 
SSAIRLSKGF YGTGETFLFS FSPQLKVFKW TGSNSFFVKG DLDSLMMGSG SGRFGLWLDG 

       190        200        210 
DLFRGGSSPC PTFNNEVLAR QEQFCIQELE AWLLS 

« Hide

References

[1]"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. expand/collapse author list , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Colon.
[2]"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.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AK123544 mRNA. Translation: BAG53910.1.
BC127688 mRNA. Translation: AAI27689.1.
BC130646 mRNA. Translation: AAI30647.1.
BC130648 mRNA. Translation: AAI30649.1.
IPIIPI00552055.
RefSeqNP_542195.1. NM_080628.1.
UniGeneHs.472630.

3D structure databases

ProteinModelPortalA0PJX2.
ModBaseSearch...

Proteomic databases

PRIDEA0PJX2.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000217320; ENSP00000217320; ENSG00000101342.
GeneID140711.
KEGGhsa:140711.
UCSCuc002xgg.1. human.

Organism-specific databases

CTD140711.
GeneCardsGC20P035504.
HGNCHGNC:16112. C20orf118.
neXtProtNX_A0PJX2.
PharmGKBPA25658.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG10214.
GeneTreeENSGT00410000025363.
HOGENOMHBG748961.
HOVERGENHBG057616.
InParanoidA0PJX2.
OMAHLLPRSM.
OrthoDBEOG4N04FZ.
PhylomeDBA0PJX2.

Gene expression databases

BgeeA0PJX2.
CleanExHS_C20orf118.
GenevestigatorA0PJX2.

Family and domain databases

InterProIPR006571. TLDc.
[Graphical view]
PfamPF07534. TLD. 1 hit.
[Graphical view]
SMARTSM00584. TLDc. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio84287.

Entry information

Entry nameCT118_HUMAN
AccessionPrimary (citable) accession number: A0PJX2
Secondary accession number(s): B3KVU8
Entry history
Integrated into UniProtKB/Swiss-Prot: February 26, 2008
Last sequence update: January 9, 2007
Last modified: January 25, 2012
This is version 38 of the entry and version 1 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 20

Human chromosome 20: 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