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Q9BTA0 (F167B_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified July 9, 2014. Version 86. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (2) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Protein FAM167B
Gene names
Name:FAM167B
Synonyms:C1orf90
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length163 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Sequence similarities

Belongs to the FAM167 (SEC) family.

Ontologies

Keywords
   DomainCoiled coil
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
None. [Check GOA]

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 163163Protein FAM167B
PRO_0000221434

Regions

Coiled coil73 – 13260 Potential

Sequences

Sequence LengthMass (Da)Tools
Q9BTA0 [UniParc].

Last modified February 6, 2007. Version 2.
Checksum: 7C1F3BF627C4DB60

FASTA16318,414
        10         20         30         40         50         60 
MSLGLLKFQA VGEEDEEDEE GESLDSVKAL TAKLQLQTRR PSYLEWTAQV QSQAWRRAQA 

        70         80         90        100        110        120 
KPGPGGPGDI CGFDSMDSAL EWLRRELREM QAQDRQLAGQ LLRLRAQLHR LKMDQACHLH 

       130        140        150        160 
QELLDEAELE LELEPGAGLA LAPLLRHLGL TRMNISARRF TLC 

« Hide

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].
Tissue: Melanoma.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL121991 Genomic DNA. Translation: CAI22319.2.
BC004269 mRNA. Translation: AAH04269.2.
CCDSCCDS358.2.
RefSeqNP_116037.2. NM_032648.2.
UniGeneHs.18449.

3D structure databases

ProteinModelPortalQ9BTA0.
ModBaseSearch...
MobiDBSearch...

PTM databases

PhosphoSiteQ9BTA0.

Polymorphism databases

DMDM125987799.

Proteomic databases

PaxDbQ9BTA0.
PRIDEQ9BTA0.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000373582; ENSP00000362684; ENSG00000183615.
GeneID84734.
KEGGhsa:84734.
UCSCuc001buw.3. human.

Organism-specific databases

CTD84734.
GeneCardsGC01P032712.
HGNCHGNC:28133. FAM167B.
HPAHPA029398.
neXtProtNX_Q9BTA0.
PharmGKBPA162387068.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG271116.
HOGENOMHOG000004827.
HOVERGENHBG074242.
InParanoidQ9BTA0.
OMAKVDQVCH.
OrthoDBEOG7JMGG3.
PhylomeDBQ9BTA0.
TreeFamTF330468.

Gene expression databases

BgeeQ9BTA0.
CleanExHS_FAM167B.
GenevestigatorQ9BTA0.

Family and domain databases

InterProIPR024280. FAM167.
[Graphical view]
PfamPF11652. DUF3259. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

GenomeRNAi84734.
NextBio74856.
PROQ9BTA0.

Entry information

Entry nameF167B_HUMAN
AccessionPrimary (citable) accession number: Q9BTA0
Secondary accession number(s): Q5TDH6
Entry history
Integrated into UniProtKB/Swiss-Prot: January 27, 2003
Last sequence update: February 6, 2007
Last modified: July 9, 2014
This is version 86 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

SIMILARITY comments

Index of protein domains and families

Human chromosome 1

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