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Reviewed, UniProtKB/Swiss-Prot Q5JX71 (CT106_HUMAN)

Last modified December 16, 2008. Version 25. 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 C20orf106
Gene names
Name: C20orf106
OrganismHomo sapiens (Human)
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 transcript level.

General annotation (Comments)

Subcellular location

Membrane; Single-pass type I membrane proteinPotential.

Sequence caution

The sequence AAH29411.1 differs from that shown. Reason: Miscellaneous discrepancy. Contaminating sequence. Potential poly-A sequence.

Ontologies

Keywords

   Cellular componentMembrane
   Coding sequence diversityPolymorphism
   DomainCoiled coil
Signal
Transmembrane

Gene Ontology (GO)

   Cellular componentintegral to membrane

Inferred from electronic annotation. Source: UniProtKB-KW

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 1919 Potential
Chain20 – 171152Uncharacterized protein C20orf106
PRO_0000264155

Regions

Topological domain20 – 5233Extracellular Potential
Transmembrane53 – 7321 Potential
Topological domain74 – 17198Cytoplasmic Potential
Coiled coil114 – 13926 Potential

Natural variations

Natural variant661V → A: dbSNP rs707554.
VAR_029621
Natural variant951L → F: dbSNP rs1054343.
VAR_033761
Natural variant1171M → K: dbSNP rs1054349.
VAR_029622
Natural variant1351R → G: dbSNP rs1054358.
VAR_029623
Natural variant1461R → K: dbSNP rs1054361.
VAR_029624

Experimental info

Sequence conflict981P → L in AAH29411. Ref.2

Sequences

Sequence LengthMass (Da)Tools
Q5JX71-1 [UniParc].

Last modified February 15, 2005. Version 1.
Checksum: 2CBB21C35AF9623A

FASTA17119,603
        10         20         30         40         50         60 
MWTLKSSLVL LLCLTCSYAF MFSSLRQKTS EPQGKVQYGE HFRIRQNLPE HTQGWLGSKW 

        70         80         90        100        110        120 
LWLLFVVVPF VILQCQRDSE KNKEQSPPGL RGGQLHSPLK KKRNASPNKD CAFNTLMELE 

       130        140        150        160        170 
VELMKFVSKV RNLKRAMATG SGSNLRLRKS EMPADPYHVT ICEIWGEESS S 

« 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: 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].
Tissue: Testis.

Cross-references

Sequence databases

AL109806 Genomic DNA. Translation: CAI19289.1.
BC029411 mRNA. Translation: AAH29411.1. Sequence problems.
BC107704 mRNA. Translation: AAI07705.1.
RefSeqNP_001012989.2.
UniGeneHs.504907

3D structure databases

ModBaseSearch...

Proteomic databases

PRIDEQ5JX71.

Genome annotation databases

EnsemblENSG00000124103. Homo sapiens. [Contig view]
GeneID200232.
KEGGhsa:200232.

Organism-specific databases

GeneCardsGC20P054532.
HGNCHGNC:16100. C20orf106.
PharmGKBPA134974173.
GenAtlasSearch...

Phylogenomic databases

HOVERGENQ5JX71.

Gene expression databases

CleanExHS_C20orf106.
GermOnlineENSG00000124103. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other Resources

NextBio89874.

Entry information

Entry nameCT106_HUMAN
AccessionPrimary (citable) accession number: Q5JX71
Secondary accession number(s): Q05C43
Entry history
Integrated into UniProtKB/Swiss-Prot: December 12, 2006
Last sequence update: February 15, 2005
Last modified: December 16, 2008
This is version 25 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)

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