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Q8N910 (CO056_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 16, 2014. Version 61. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (3) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Putative uncharacterized protein C15orf56
Gene names
Name:C15orf56
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length161 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

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 – 161161Putative uncharacterized protein C15orf56
PRO_0000317190

Natural variations

Natural variant1191P → S.
Corresponds to variant rs55863440 [ dbSNP | Ensembl ].
VAR_061614
Natural variant1511P → R.
Corresponds to variant rs55974545 [ dbSNP | Ensembl ].
VAR_061615
Natural variant1601I → T.
Corresponds to variant rs55799438 [ dbSNP | Ensembl ].
VAR_061616

Sequences

Sequence LengthMass (Da)Tools
Q8N910 [UniParc].

Last modified October 1, 2002. Version 1.
Checksum: F2F46991878661C1

FASTA16117,040
        10         20         30         40         50         60 
MPRAGRAPAE GGPAPGTRSS RCLRPRPLAW RRLVPNFGAW APRKGAARVG RPVLSPRTSG 

        70         80         90        100        110        120 
AAGEPTCGAG SPGTLEEGVA SGRTRRRTQS AGEVAKCRWG LGQEPLCPRG AVLLNSFSPP 

       130        140        150        160 
AWPQFPPALR LRALAWPQPR GPACGSTAQW PPRGDPTWRI S 

« 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] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Heart.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AK095915 mRNA. Translation: BAC04647.1.
RefSeqNP_001034994.1. NM_001039905.2.
UniGeneHs.631718.

3D structure databases

ProteinModelPortalQ8N910.
ModBaseSearch...
MobiDBSearch...

Proteomic databases

PRIDEQ8N910.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000319503; ENSP00000315794; ENSG00000176753.
GeneID644809.
KEGGhsa:644809.
UCSCuc001zla.2. human.

Organism-specific databases

CTD644809.
GeneCardsGC15M040542.
HGNCHGNC:33868. C15orf56.
HPAHPA046873.
neXtProtNX_Q8N910.
PharmGKBPA162378225.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG126954.
HOGENOMHOG000111859.
InParanoidQ8N910.
OMAGPACGST.
OrthoDBEOG7GXPD3.
TreeFamTF342135.

Gene expression databases

BgeeQ8N910.
CleanExHS_C15orf56.
GenevestigatorQ8N910.

Family and domain databases

ProtoNetSearch...

Other

NextBio116680.

Entry information

Entry nameCO056_HUMAN
AccessionPrimary (citable) accession number: Q8N910
Entry history
Integrated into UniProtKB/Swiss-Prot: February 5, 2008
Last sequence update: October 1, 2002
Last modified: April 16, 2014
This is version 61 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 polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human chromosome 15

Human chromosome 15: entries, gene names and cross-references to MIM