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Reviewed, UniProtKB/Swiss-Prot Q5JX69 (CT107_HUMAN)

Last modified November 24, 2009. Version 35. 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 · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Uncharacterized protein C20orf107
Gene names
Name: C20orf107
OrganismHomo sapiens (Human) [Complete proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length171 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at protein level.

General annotation (Comments)

Subcellular location

Membrane; Single-pass type I membrane protein Potential.

Ontologies

Keywords
   Cellular componentMembrane
   Coding sequence diversityPolymorphism
   DomainSignal
Transmembrane
   PTMPhosphoprotein
   Technical termComplete proteome
Gene Ontology (GO)
   Cellular componentintegral to membrane

Inferred from electronic annotation. Source: UniProtKB-SubCell

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 1919 Potential
Chain20 – 171152Uncharacterized protein C20orf107
PRO_0000236040

Regions

Topological domain20 – 5233Extracellular Potential
Transmembrane53 – 7321 Potential
Topological domain74 – 17198Cytoplasmic Potential

Amino acid modifications

Modified residue1411Phosphoserine Ref.3
Modified residue1431Phosphoserine Ref.3

Natural variations

Natural variant741Q → K: dbSNP rs3209183. Ref.2
VAR_050918
Natural variant1291E → A: dbSNP rs2296129.
VAR_033762

Experimental info

Sequence conflict37 – 382PC → QY in AAI05793. Ref.2

Sequences

Sequence LengthMass (Da)Tools
Q5JX69-1 [UniParc].

Last modified February 15, 2005. Version 1.
Checksum: 8B24B54EB89505A8

FASTA17119,499
        10         20         30         40         50         60 
MWTLKSSLVL LLCLTCSYAF MFSSLRQKTS EPQGKVPCGE HFRIRQNLPE HTQGWLGSKW 

        70         80         90        100        110        120 
LWLLFAVVPF VILQCQRDSE KNKEQSPPGL RGFPFRTPLK KNQNASLYKD CVFNTLNELE 

       130        140        150        160        170 
VELLKFVSEV QNLKGAMATG SGSNLKLRRS EMPADPYHVT ICKIWGEESS S 

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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: 11780052] [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], VARIANT LYS-74.
Tissue: Testis.
[3]"Phosphoproteome analysis of capacitated human sperm. Evidence of tyrosine phosphorylation of a kinase-anchoring protein 3 and valosin-containing protein/p97 during capacitation."
Ficarro S., Chertihin O., Westbrook V.A., White F., Jayes F., Kalab P., Marto J.A., Shabanowitz J., Herr J.C., Hunt D.F., Visconti P.E.
J. Biol. Chem. 278:11579-11589(2003) [PubMed: 12509440] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-141 AND SER-143, MASS SPECTROMETRY.
Tissue: Sperm.

Cross-references

Sequence databases

AL109806 Genomic DNA. Translation: CAI19291.1.
BC105792 mRNA. Translation: AAI05793.1.
IPIIPI00374077.
RefSeqNP_001013668.2.
UniGeneHs.287759

3D structure databases

ModBaseSearch...

PTM databases

PhosphoSiteQ5JX69.

Genome annotation databases

EnsemblENST00000371325; ENSP00000360376; ENSG00000213714; Homo sapiens. [Genome view]
GeneID388799.
KEGGhsa:388799.
UCSCuc002xxy.1. human.

Organism-specific databases

CTD388799.
GeneCardsGC20P054541.
HGNCHGNC:16101. C20orf107.
PharmGKBPA25646.
GenAtlasSearch...

Phylogenomic databases

HOVERGENQ5JX69.
OMALPEYAQG
OrthoDBEOG9D81SD

Gene expression databases

ArrayExpressQ5JX69.
BgeeQ5JX69.
CleanExHS_C20orf107.
GenevestigatorQ5JX69.
GermOnlineENSG00000124103. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other Resources

NextBio102369.

Entry information

Entry nameCT107_HUMAN
AccessionPrimary (citable) accession number: Q5JX69
Secondary accession number(s): Q3KRB5
Entry history
Integrated into UniProtKB/Swiss-Prot: May 16, 2006
Last sequence update: February 15, 2005
Last modified: November 24, 2009
This is version 35 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 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

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