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Q5VZQ5 (CJ122_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 51. 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 C10orf122
Gene names
Name:C10orf122
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length186 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 – 186186Putative uncharacterized protein C10orf122
PRO_0000244088

Natural variations

Natural variant381E → Q.
Corresponds to variant rs9422915 [ dbSNP | Ensembl ].
VAR_059615

Sequences

Sequence LengthMass (Da)Tools
Q5VZQ5 [UniParc].

Last modified December 7, 2004. Version 1.
Checksum: 6C482FF5E5155E00

FASTA18621,545
        10         20         30         40         50         60 
MTKGRRFNPP SDKDGRWFPH IGLTQKTPES ITSATSKEPQ SPHLPRQAEG KLPPIYKVRE 

        70         80         90        100        110        120 
KQAVNNQFPF SVHDNRHSLE NSGCYLDSGL GRKKISPDKR QHVSRNFNLW ACDYVPSCLD 

       130        140        150        160        170        180 
GFSNNQISYV YKEAMVVSSF RRFPRCYKEI WNAFTFLPER SYTEVLKKKP KVRFTVDKKV 


VSSLES 

« Hide

References

[1]"The DNA sequence and comparative analysis of human chromosome 10."
Deloukas P., Earthrowl M.E., Grafham D.V., Rubenfield M., French L., Steward C.A., Sims S.K., Jones M.C., Searle S., Scott C., Howe K., Hunt S.E., Andrews T.D., Gilbert J.G.R., Swarbreck D., Ashurst J.L., Taylor A., Battles J. expand/collapse author list , Bird C.P., Ainscough R., Almeida J.P., Ashwell R.I.S., Ambrose K.D., Babbage A.K., Bagguley C.L., Bailey J., Banerjee R., Bates K., Beasley H., Bray-Allen S., Brown A.J., Brown J.Y., Burford D.C., Burrill W., Burton J., Cahill P., Camire D., Carter N.P., Chapman J.C., Clark S.Y., Clarke G., Clee C.M., Clegg S., Corby N., Coulson A., Dhami P., Dutta I., Dunn M., Faulkner L., Frankish A., Frankland J.A., Garner P., Garnett J., Gribble S., Griffiths C., Grocock R., Gustafson E., Hammond S., Harley J.L., Hart E., Heath P.D., Ho T.P., Hopkins B., Horne J., Howden P.J., Huckle E., Hynds C., Johnson C., Johnson D., Kana A., Kay M., Kimberley A.M., Kershaw J.K., Kokkinaki M., Laird G.K., Lawlor S., Lee H.M., Leongamornlert D.A., Laird G., Lloyd C., Lloyd D.M., Loveland J., Lovell J., McLaren S., McLay K.E., McMurray A., Mashreghi-Mohammadi M., Matthews L., Milne S., Nickerson T., Nguyen M., Overton-Larty E., Palmer S.A., Pearce A.V., Peck A.I., Pelan S., Phillimore B., Porter K., Rice C.M., Rogosin A., Ross M.T., Sarafidou T., Sehra H.K., Shownkeen R., Skuce C.D., Smith M., Standring L., Sycamore N., Tester J., Thorpe A., Torcasso W., Tracey A., Tromans A., Tsolas J., Wall M., Walsh J., Wang H., Weinstock K., West A.P., Willey D.L., Whitehead S.L., Wilming L., Wray P.W., Young L., Chen Y., Lovering R.C., Moschonas N.K., Siebert R., Fechtel K., Bentley D., Durbin R.M., Hubbard T., Doucette-Stamm L., Beck S., Smith D.R., Rogers J.
Nature 429:375-381(2004) [PubMed: 15164054] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[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: Testis.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL158835 Genomic DNA. Translation: CAH73213.1.
BC062717 mRNA. Translation: AAH62717.1.
IPIIPI00375813.
RefSeqNP_001121674.1. NM_001128202.1.
UniGeneHs.148259.

3D structure databases

ProteinModelPortalQ5VZQ5.
ModBaseSearch...

Polymorphism databases

DMDM74747835.

Proteomic databases

PRIDEQ5VZQ5.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000368821; ENSP00000357811; ENSG00000175018.
GeneID387718.
KEGGhsa:387718.
UCSCuc001lik.2. human.

Organism-specific databases

CTD387718.
GeneCardsGC10M127255.
HGNCHGNC:31653. C10orf122.
neXtProtNX_Q5VZQ5.
PharmGKBPA134969142.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG14570.
GeneTreeENSGT00390000012491.
HOGENOMHBG126800.
HOVERGENHBG059346.
InParanoidQ5VZQ5.
OMAFRRFPRC.
OrthoDBEOG4PRSRQ.
PhylomeDBQ5VZQ5.

Gene expression databases

ArrayExpressQ5VZQ5.
BgeeQ5VZQ5.
CleanExHS_C10orf122.
GenevestigatorQ5VZQ5.
GermOnlineENSG00000175018. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other

NextBio101545.

Entry information

Entry nameCJ122_HUMAN
AccessionPrimary (citable) accession number: Q5VZQ5
Secondary accession number(s): Q0P5T8
Entry history
Integrated into UniProtKB/Swiss-Prot: June 27, 2006
Last sequence update: December 7, 2004
Last modified: January 25, 2012
This is version 51 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 10

Human chromosome 10: 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