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Reviewed, UniProtKB/Swiss-Prot Q8IYD9 (CR054_HUMAN)

Last modified November 24, 2009. Version 50. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (3) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Uncharacterized protein C18orf54
Gene names
Name: C18orf54
OrganismHomo sapiens (Human) [Complete proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length372 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 Potential.

Ontologies

Keywords
   Cellular componentSecreted
   Coding sequence diversityAlternative splicing
Polymorphism
   DomainSignal
   Technical termComplete proteome
Gene Ontology (GO)
   Cellular componentextracellular region

Inferred from electronic annotation. Source: UniProtKB-SubCell

Complete GO annotation...

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q8IYD9-1)

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.
Isoform 2 (identifier: Q8IYD9-2)

The sequence of this isoform differs from the canonical sequence as follows:
     197-197: G → GRLKNPKLMN...PGQSTKPFSG
Note: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 3131 Potential
Chain32 – 372341Uncharacterized protein C18orf54
PRO_0000019561

Natural variations

Alternative sequence1971G → GRLKNPKLMNRTNNCISESS LSFPKKSSFKDSSEHSLEKN YPRWLTSQKSDLNVSGITSI PDFKYPVWLHNQDLLPDANS QRVYQIFKDDQCSPRHSHQA QGTSRLINKLDCFEYAFEPS NFSNSLSDDKELVNEYKCDF EHSQCQCENPLLPGQSTKPF SG in isoform 2.
VSP_015085
Natural variant1471R → P: dbSNP rs1657907.
VAR_050903
Natural variant1961C → F: dbSNP rs16958096.
VAR_050904

Experimental info

Sequence conflict1021K → E in CAE45934. Ref.1
Sequence conflict1141T → I in CAE45934. Ref.1

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified March 1, 2003. Version 1.
Checksum: F4BCD1BEA28FF61E

FASTA37241,811
        10         20         30         40         50         60 
MAKSKTKHRL CSQESSVSAL LASCTLSGSN SSNSDGSFHY KDKLYRSASQ ALQAYIDDFD 

        70         80         90        100        110        120 
LGQIYPGAST GKINIDEDFT NMSQFCNYIY KPNNAFENLD HKKHSNFISC RRHTVNDIDS 

       130        140        150        160        170        180 
MSLTTDDLLR LPADGSFSYT YVGPSHRTSK KNKKCRGRLG SLDIEKNPHF QGPYTSMGKD 

       190        200        210        220        230        240 
NFVTPVIRSN INGKQCGDKI ELLILKAKRN LEQCTEELPK SMKKDDSPCS LDKLEADRSW 

       250        260        270        280        290        300 
ENIPVTFKSP VPVNSDDSPQ QTSRAKSAKG VLEDFLNNDN QSCTLSGGKH HGPVEALKQM 

       310        320        330        340        350        360 
LFNLQAVQER FNQNKTTDPK EEIKQVSEDD FSKLQLKESM IPITRSLQKA LHHLSRLRDL 

       370 
VDDTNGERSP KM 

« Hide

Isoform 2.

Checksum: FE15C3FFA41DFC41
Show »

FASTA53360,320

References

[1]"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: 17974005] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
Tissue: Uterine endothelium.
[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] (ISOFORM 1).
Tissue: Testis.
[3]"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] OF 88-372 (ISOFORM 2).
Tissue: Uterus.

Cross-references

Sequence databases

BX640877 mRNA. Translation: CAE45934.1.
BC036054 mRNA. Translation: AAH36054.1.
AK126503 mRNA. Translation: BAC86570.1. Different initiation.
IPIIPI00217756.
IPI00445152.
RefSeqNP_775800.3.
UniGeneHs.208701

3D structure databases

ModBaseSearch...

Protein-protein interaction databases

IntActQ8IYD9. 1 interaction.

Proteomic databases

PRIDEQ8IYD9.

Genome annotation databases

EnsemblENST00000300091; ENSP00000300091; ENSG00000166845; Homo sapiens. [Genome view]
GeneID162681.
KEGGhsa:162681.
UCSCuc002lfn.2. human.
uc002lfo.2. human.

Organism-specific databases

CTD162681.
GeneCardsGC18P050140.
HGNCHGNC:13796. C18orf54.
PharmGKBPA134942612.
GenAtlasSearch...

Phylogenomic databases

HOVERGENQ8IYD9.
OMAMKKDDSP
OrthoDBEOG99W51M

Enzyme and pathway databases

BioCycCATTLE:ENSBTAG00000008169-MON.

Gene expression databases

ArrayExpressQ8IYD9.
BgeeQ8IYD9.
CleanExHS_C18orf54.
GenevestigatorQ8IYD9.
GermOnlineENSG00000166845. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other Resources

NextBio88212.

Entry information

Entry nameCR054_HUMAN
AccessionPrimary (citable) accession number: Q8IYD9
Secondary accession number(s): Q6MZU3, Q6ZTL6
Entry history
Integrated into UniProtKB/Swiss-Prot: August 16, 2005
Last sequence update: March 1, 2003
Last modified: November 24, 2009
This is version 50 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)
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 18

Human chromosome 18: 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

Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents