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Q8N1D5 (CA158_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified June 11, 2014. Version 72. 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 C1orf158
Gene names
Name:C1orf158
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length194 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 – 194194Uncharacterized protein C1orf158
PRO_0000247260

Natural variations

Natural variant1911F → L. Ref.2
Corresponds to variant rs1132185 [ dbSNP | Ensembl ].
VAR_027091

Sequences

Sequence LengthMass (Da)Tools
Q8N1D5 [UniParc].

Last modified July 25, 2006. Version 2.
Checksum: 23471567BC85238F

FASTA19423,067
        10         20         30         40         50         60 
MFLTAVNPQP LSTPSWQIET KYSTKVLTGN WMEERRKFTR DTDKTPQSIY RKEYIPFPDH 

        70         80         90        100        110        120 
RPDQISRWYG KRKVEGLPYK HLITHHQEPP HRYLISTYDD HYNRHGYNPG LPPLRTWNGQ 

       130        140        150        160        170        180 
KLLWLPEKSD FPLLAPPTNY GLYEQLKQRQ LTPKAGLKQS TYTSSYPRPP LCAMSWREHA 

       190 
VPVPPHRLHP FPHF 

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References

[1]"The DNA sequence and biological annotation of human chromosome 1."
Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A., Jones M.C., Gillson C., Searle S., Zhou Y., Kokocinski F., McDonald L., Evans R., Phillips K. expand/collapse author list , Atkinson A., Cooper R., Jones C., Hall R.E., Andrews T.D., Lloyd C., Ainscough R., Almeida J.P., Ambrose K.D., Anderson F., Andrew R.W., Ashwell R.I.S., Aubin K., Babbage A.K., Bagguley C.L., Bailey J., Beasley H., Bethel G., Bird C.P., Bray-Allen S., Brown J.Y., Brown A.J., Buckley D., Burton J., Bye J., Carder C., Chapman J.C., Clark S.Y., Clarke G., Clee C., Cobley V., Collier R.E., Corby N., Coville G.J., Davies J., Deadman R., Dunn M., Earthrowl M., Ellington A.G., Errington H., Frankish A., Frankland J., French L., Garner P., Garnett J., Gay L., Ghori M.R.J., Gibson R., Gilby L.M., Gillett W., Glithero R.J., Grafham D.V., Griffiths C., Griffiths-Jones S., Grocock R., Hammond S., Harrison E.S.I., Hart E., Haugen E., Heath P.D., Holmes S., Holt K., Howden P.J., Hunt A.R., Hunt S.E., Hunter G., Isherwood J., James R., Johnson C., Johnson D., Joy A., Kay M., Kershaw J.K., Kibukawa M., Kimberley A.M., King A., Knights A.J., Lad H., Laird G., Lawlor S., Leongamornlert D.A., Lloyd D.M., Loveland J., Lovell J., Lush M.J., Lyne R., Martin S., Mashreghi-Mohammadi M., Matthews L., Matthews N.S.W., McLaren S., Milne S., Mistry S., Moore M.J.F., Nickerson T., O'Dell C.N., Oliver K., Palmeiri A., Palmer S.A., Parker A., Patel D., Pearce A.V., Peck A.I., Pelan S., Phelps K., Phillimore B.J., Plumb R., Rajan J., Raymond C., Rouse G., Saenphimmachak C., Sehra H.K., Sheridan E., Shownkeen R., Sims S., Skuce C.D., Smith M., Steward C., Subramanian S., Sycamore N., Tracey A., Tromans A., Van Helmond Z., Wall M., Wallis J.M., White S., Whitehead S.L., Wilkinson J.E., Willey D.L., Williams H., Wilming L., Wray P.W., Wu Z., Coulson A., Vaudin M., Sulston J.E., Durbin R.M., Hubbard T., Wooster R., Dunham I., Carter N.P., McVean G., Ross M.T., Harrow J., Olson M.V., Beck S., Rogers J., Bentley D.R.
Nature 441:315-321(2006) [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], VARIANT LEU-191.
Tissue: Brain.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL513016 Genomic DNA. Translation: CAH74178.1.
BC029894 mRNA. Translation: AAH29894.1.
RefSeqNP_689503.3. NM_152290.3.
UniGeneHs.98095.

3D structure databases

ProteinModelPortalQ8N1D5.
ModBaseSearch...
MobiDBSearch...

Protein-protein interaction databases

STRING9606.ENSP00000288048.

PTM databases

PhosphoSiteQ8N1D5.

Proteomic databases

PaxDbQ8N1D5.
PRIDEQ8N1D5.

Protocols and materials databases

DNASU93190.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000288048; ENSP00000288048; ENSG00000157330.
GeneID93190.
KEGGhsa:93190.
UCSCuc001auh.3. human.

Organism-specific databases

CTD93190.
GeneCardsGC01P012806.
HGNCHGNC:28567. C1orf158.
HPAHPA028396.
neXtProtNX_Q8N1D5.
PharmGKBPA142672409.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG42024.
HOGENOMHOG000231101.
HOVERGENHBG059152.
InParanoidQ8N1D5.
OMAYRKEYVP.
OrthoDBEOG7KQ22H.
PhylomeDBQ8N1D5.
TreeFamTF328903.

Gene expression databases

ArrayExpressQ8N1D5.
BgeeQ8N1D5.
CleanExHS_C1orf158.
GenevestigatorQ8N1D5.

Family and domain databases

ProtoNetSearch...

Other

GenomeRNAi93190.
NextBio78027.

Entry information

Entry nameCA158_HUMAN
AccessionPrimary (citable) accession number: Q8N1D5
Secondary accession number(s): Q5VUY4
Entry history
Integrated into UniProtKB/Swiss-Prot: July 25, 2006
Last sequence update: July 25, 2006
Last modified: June 11, 2014
This is version 72 of the entry and version 2 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 polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human chromosome 1

Human chromosome 1: entries, gene names and cross-references to MIM