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Q9H1P6 (CT085_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 3, 2013. Version 67. 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 C20orf85
Gene names
Name:C20orf85
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length137 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 – 137137Uncharacterized protein C20orf85
PRO_0000079448

Natural variations

Natural variant261R → H.
Corresponds to variant rs16984945 [ dbSNP | Ensembl ].
VAR_033759
Natural variant341R → Q.
Corresponds to variant rs45576936 [ dbSNP | Ensembl ].
VAR_061632
Natural variant991I → V.
Corresponds to variant rs17440813 [ dbSNP | Ensembl ].
VAR_033760

Sequences

Sequence LengthMass (Da)Tools
Q9H1P6 [UniParc].

Last modified March 1, 2001. Version 1.
Checksum: 9EDB8FF6FA3CD923

FASTA13715,719
        10         20         30         40         50         60 
MAQKPLSTAA AERMNLVGQD EIWKYRLKAE SEARQNWPQN WGFLTTPFEE LIKCEEDLPT 

        70         80         90        100        110        120 
PKPKIELPER FRIRPVTPVE KYIKVFPSPP VPQTTQGFIG WRSAVPGLNK CLELDDAIRS 

       130 
CKGAFARELC WPKQGVH 

« Hide

References

[1]"The DNA sequence and comparative analysis of human chromosome 20."
Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L., Bailey J., Barlow K.F., Bates K.N., Beard L.M., Beare D.M., Beasley O.P., Bird C.P., Blakey S.E. expand/collapse author list , Bridgeman A.M., Brown A.J., Buck D., Burrill W.D., Butler A.P., Carder C., Carter N.P., Chapman J.C., Clamp M., Clark G., Clark L.N., Clark S.Y., Clee C.M., Clegg S., Cobley V.E., Collier R.E., Connor R.E., Corby N.R., Coulson A., Coville G.J., Deadman R., Dhami P.D., Dunn M., Ellington A.G., Frankland J.A., Fraser A., French L., Garner P., Grafham D.V., Griffiths C., Griffiths M.N.D., Gwilliam R., Hall R.E., Hammond S., Harley J.L., Heath P.D., Ho S., Holden J.L., Howden P.J., Huckle E., Hunt A.R., Hunt S.E., Jekosch K., Johnson C.M., Johnson D., Kay M.P., Kimberley A.M., King A., Knights A., Laird G.K., Lawlor S., Lehvaeslaiho M.H., Leversha M.A., Lloyd C., Lloyd D.M., Lovell J.D., Marsh V.L., Martin S.L., McConnachie L.J., McLay K., McMurray A.A., Milne S.A., Mistry D., Moore M.J.F., Mullikin J.C., Nickerson T., Oliver K., Parker A., Patel R., Pearce T.A.V., Peck A.I., Phillimore B.J.C.T., Prathalingam S.R., Plumb R.W., Ramsay H., Rice C.M., Ross M.T., Scott C.E., Sehra H.K., Shownkeen R., Sims S., Skuce C.D., Smith M.L., Soderlund C., Steward C.A., Sulston J.E., Swann R.M., Sycamore N., Taylor R., Tee L., Thomas D.W., Thorpe A., Tracey A., Tromans A.C., Vaudin M., Wall M., Wallis J.M., Whitehead S.L., Whittaker P., Willey D.L., Williams L., Williams S.A., Wilming L., Wray P.W., Hubbard T., Durbin R.M., Bentley D.R., Beck S., Rogers J.
Nature 414:865-871(2001) [PubMed] [Europe PMC] [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] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Brain.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL354776 Genomic DNA. Translation: CAC17564.1.
BC035405 mRNA. Translation: AAH35405.1.
IPIIPI00011788.
RefSeqNP_848551.1. NM_178456.2.
UniGeneHs.43977.

3D structure databases

ProteinModelPortalQ9H1P6.
ModBaseSearch...

Proteomic databases

PaxDbQ9H1P6.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000371168; ENSP00000360210; ENSG00000124237.
GeneID128602.
KEGGhsa:128602.
UCSCuc002xyv.3. human.

Organism-specific databases

CTD128602.
GeneCardsGC20P056726.
HGNCHGNC:16216. C20orf85.
neXtProtNX_Q9H1P6.
PharmGKBPA25793.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG46284.
HOGENOMHOG000276533.
HOVERGENHBG051179.
InParanoidQ9H1P6.
OMAEIWKYRL.
OrthoDBEOG4DV5NM.
PhylomeDBQ9H1P6.

Gene expression databases

BgeeQ9H1P6.
CleanExHS_C20orf85.
GenevestigatorQ9H1P6.
GermOnlineENSG00000124237. Homo sapiens.

Family and domain databases

InterProIPR020339. Uncharacterised_C20orf85.
[Graphical view]
ProDomPD297655. C20orf85_euk. 1 hit.
[Graphical view] [Entries sharing at least one domain]
ProtoNetSearch...

Other

GenomeRNAi128602.
NextBio82390.

Entry information

Entry nameCT085_HUMAN
AccessionPrimary (citable) accession number: Q9H1P6
Entry history
Integrated into UniProtKB/Swiss-Prot: January 10, 2003
Last sequence update: March 1, 2001
Last modified: April 3, 2013
This is version 67 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 20

Human chromosome 20: 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