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A2RUQ5 (CQ102_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified February 19, 2014. Version 49. 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:
Uncharacterized protein C17orf102
Gene names
Name:C17orf102
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length167 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 – 167167Uncharacterized protein C17orf102
PRO_0000348468

Natural variations

Natural variant981G → R. Ref.1
Corresponds to variant rs58529418 [ dbSNP | Ensembl ].
VAR_046187
Natural variant1551R → K. Ref.1 Ref.2
Corresponds to variant rs887230 [ dbSNP | Ensembl ].
VAR_046188

Experimental info

Sequence conflict1121A → P in BAC86680. Ref.1

Sequences

Sequence LengthMass (Da)Tools
A2RUQ5 [UniParc].

Last modified March 6, 2007. Version 1.
Checksum: 361507D8781DE492

FASTA16717,761
        10         20         30         40         50         60 
MFDFSFPTPA SAGTRMGPAS CGGRSLHLPQ LRFSRVDATA VTDVPFQRMH APHRAPEVFC 

        70         80         90        100        110        120 
SRSSRGAGRG HPTPTPRVRW ALAGNQPRCC AQLLSGRGGS GAQLRAGWVR GAAVGNLFIL 

       130        140        150        160 
LLGKEDGEEE GTVLSYSSMV HISNITGIVG TTVSRTKPAL VLMELTF 

« 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], VARIANTS ARG-98 AND LYS-155.
Tissue: Cerebellum.
[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] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT LYS-155.
Tissue: Brain.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AK126768 mRNA. Translation: BAC86680.1.
BC133004 mRNA. Translation: AAI33005.1.
BC136710 mRNA. Translation: AAI36711.1.
BC142651 mRNA. Translation: AAI42652.1.
RefSeqNP_997337.2. NM_207454.2.
UniGeneHs.514090.

3D structure databases

ProteinModelPortalA2RUQ5.
ModBaseSearch...
MobiDBSearch...

PTM databases

PhosphoSiteA2RUQ5.

Proteomic databases

PaxDbA2RUQ5.
PRIDEA2RUQ5.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000357754; ENSP00000350392; ENSG00000197322.
GeneID400591.
KEGGhsa:400591.
UCSCuc002hie.1. human.

Organism-specific databases

CTD400591.
GeneCardsGC17M032901.
HGNCHGNC:34412. C17orf102.
HPAHPA043259.
neXtProtNX_A2RUQ5.
PharmGKBPA164716932.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG73773.
HOGENOMHOG000111947.
InParanoidA2RUQ5.
OMAAGNQPRC.
OrthoDBEOG75TMDF.
PhylomeDBA2RUQ5.
TreeFamTF353629.

Gene expression databases

BgeeA2RUQ5.
GenevestigatorA2RUQ5.

Family and domain databases

ProtoNetSearch...

Other

GenomeRNAi400591.
NextBio106015.

Entry information

Entry nameCQ102_HUMAN
AccessionPrimary (citable) accession number: A2RUQ5
Secondary accession number(s): A5PKX0, Q6ZTB3
Entry history
Integrated into UniProtKB/Swiss-Prot: September 2, 2008
Last sequence update: March 6, 2007
Last modified: February 19, 2014
This is version 49 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 17

Human chromosome 17: entries, gene names and cross-references to MIM