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Q8N6G2 (CM026_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 58. 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 C13orf26
Gene names
Name:C13orf26
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length289 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 – 289289Uncharacterized protein C13orf26
PRO_0000263723

Natural variations

Natural variant2311K → N.
Corresponds to variant rs9533168 [ dbSNP | Ensembl ].
VAR_029615

Sequences

Sequence LengthMass (Da)Tools
Q8N6G2 [UniParc].

Last modified October 1, 2002. Version 1.
Checksum: 294036CFF17B11F6

FASTA28933,595
        10         20         30         40         50         60 
MEQPGPRAPD PSLCHHNLQP TDDPNWDSYA TTMRTAFTPK TGAVPALIRQ NGIRRLGYTY 

        70         80         90        100        110        120 
SLSDPILNQT QYSDEYTWKS HSKEDLIKTE TSRGIKSHKS HLNEDIFLWT LPHCQQTGTL 

       130        140        150        160        170        180 
KNCLPWKIPA SMKEVNKALS NQFISLTKRD FVDRSKAQKI KKSSHLSLEW KKLLPQPPDT 

       190        200        210        220        230        240 
EFRRNYQIPA KIPELQDFSF KYGCYSSLPV ASQGLVPSVL HSYLRNQEHT KKQTTYQSDY 

       250        260        270        280 
DKTYPDFLML LNSFTSSQVK EYLQSLSYKD RQIIDRFIRT HCDTNKKKK 

« Hide

References

[1]"The DNA sequence and analysis of human chromosome 13."
Dunham A., Matthews L.H., Burton J., Ashurst J.L., Howe K.L., Ashcroft K.J., Beare D.M., Burford D.C., Hunt S.E., Griffiths-Jones S., Jones M.C., Keenan S.J., Oliver K., Scott C.E., Ainscough R., Almeida J.P., Ambrose K.D., Andrews D.T. expand/collapse author list , Ashwell R.I.S., Babbage A.K., Bagguley C.L., Bailey J., Bannerjee R., Barlow K.F., Bates K., Beasley H., Bird C.P., Bray-Allen S., Brown A.J., Brown J.Y., Burrill W., Carder C., Carter N.P., Chapman J.C., Clamp M.E., Clark S.Y., Clarke G., Clee C.M., Clegg S.C., Cobley V., Collins J.E., Corby N., Coville G.J., Deloukas P., Dhami P., Dunham I., Dunn M., Earthrowl M.E., Ellington A.G., Faulkner L., Frankish A.G., Frankland J., French L., Garner P., Garnett J., Gilbert J.G.R., Gilson C.J., Ghori J., Grafham D.V., Gribble S.M., Griffiths C., Hall R.E., Hammond S., Harley J.L., Hart E.A., Heath P.D., Howden P.J., Huckle E.J., Hunt P.J., Hunt A.R., Johnson C., Johnson D., Kay M., Kimberley A.M., King A., Laird G.K., Langford C.J., Lawlor S., Leongamornlert D.A., Lloyd D.M., Lloyd C., Loveland J.E., Lovell J., Martin S., Mashreghi-Mohammadi M., McLaren S.J., McMurray A., Milne S., Moore M.J.F., Nickerson T., Palmer S.A., Pearce A.V., Peck A.I., Pelan S., Phillimore B., Porter K.M., Rice C.M., Searle S., Sehra H.K., Shownkeen R., Skuce C.D., Smith M., Steward C.A., Sycamore N., Tester J., Thomas D.W., Tracey A., Tromans A., Tubby B., Wall M., Wallis J.M., West A.P., Whitehead S.L., Willey D.L., Wilming L., Wray P.W., Wright M.W., Young L., Coulson A., Durbin R.M., Hubbard T., Sulston J.E., Beck S., Bentley D.R., Rogers J., Ross M.T.
Nature 428:522-528(2004) [PubMed: 15057823] [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: Brain.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL353680 Genomic DNA. Translation: CAH71735.1.
BC030277 mRNA. Translation: AAH30277.1.
IPIIPI00167006.
RefSeqNP_689538.1. NM_152325.1.
UniGeneHs.124463.

3D structure databases

ProteinModelPortalQ8N6G2.
ModBaseSearch...

PTM databases

PhosphoSiteQ8N6G2.

Polymorphism databases

DMDM74751054.

Proteomic databases

PRIDEQ8N6G2.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000380473; ENSP00000369840; ENSG00000175664.
GeneID122046.
KEGGhsa:122046.
UCSCuc001uti.1. human.

Organism-specific databases

CTD122046.
GeneCardsGC13P031506.
HGNCHGNC:28622. C13orf26.
HPAHPA040455.
HPA040785.
neXtProtNX_Q8N6G2.
PharmGKBPA144596482.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG18824.
GeneTreeENSGT00390000009484.
HOGENOMHBG283141.
HOVERGENHBG056760.
InParanoidQ8N6G2.
OMAWKIPASM.
OrthoDBEOG4DJJX9.
PhylomeDBQ8N6G2.

Gene expression databases

ArrayExpressQ8N6G2.
BgeeQ8N6G2.
CleanExHS_C13orf26.
GenevestigatorQ8N6G2.
GermOnlineENSG00000175664. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other

NextBio80851.

Entry information

Entry nameCM026_HUMAN
AccessionPrimary (citable) accession number: Q8N6G2
Entry history
Integrated into UniProtKB/Swiss-Prot: December 12, 2006
Last sequence update: October 1, 2002
Last modified: January 25, 2012
This is version 58 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 13

Human chromosome 13: 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