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Q96F83 (CN079_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 16, 2014. Version 69. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (1) | 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 C14orf79
Gene names
Name:C14orf79
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length325 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

Ontologies

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

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 325325Uncharacterized protein C14orf79
PRO_0000274387

Sequences

Sequence LengthMass (Da)Tools
Q96F83 [UniParc].

Last modified February 6, 2007. Version 2.
Checksum: EDA4C63C1F4D1571

FASTA32535,690
        10         20         30         40         50         60 
MQGRRELGGE PLSDLQEEAA SASLRVAPER LSDDSLEWRR TCPDLLLSDG KASISMPREG 

        70         80         90        100        110        120 
GSTCTARCPD PGEHSSTWGE FEGFRESSAK SGQFSQSLEL LEGPTEPQPP RTTSAPKECS 

       130        140        150        160        170        180 
SHQPCQGGPW VTGTSAVPPS EPILSYENIL KCAFQEITVQ QAAEDVSTID HFLEISSEEK 

       190        200        210        220        230        240 
PGVERVHKLC NESRKLWRAL QSIHTTSTSQ RLWSESRCQE NFFLVLGIDA AQKNLSGGQG 

       250        260        270        280        290        300 
HIMEDCDLKE PEGLLTVSSF CLQHCKALIQ TKLSGPPGSK QGRLMTCSRF LKTPSCGGGQ 

       310        320 
HITIPRKRMF TPRKLKLTLF NSDVC 

« Hide

References

[1]"The DNA sequence and analysis of human chromosome 14."
Heilig R., Eckenberg R., Petit J.-L., Fonknechten N., Da Silva C., Cattolico L., Levy M., Barbe V., De Berardinis V., Ureta-Vidal A., Pelletier E., Vico V., Anthouard V., Rowen L., Madan A., Qin S., Sun H., Du H. expand/collapse author list , Pepin K., Artiguenave F., Robert C., Cruaud C., Bruels T., Jaillon O., Friedlander L., Samson G., Brottier P., Cure S., Segurens B., Aniere F., Samain S., Crespeau H., Abbasi N., Aiach N., Boscus D., Dickhoff R., Dors M., Dubois I., Friedman C., Gouyvenoux M., James R., Madan A., Mairey-Estrada B., Mangenot S., Martins N., Menard M., Oztas S., Ratcliffe A., Shaffer T., Trask B., Vacherie B., Bellemere C., Belser C., Besnard-Gonnet M., Bartol-Mavel D., Boutard M., Briez-Silla S., Combette S., Dufosse-Laurent V., Ferron C., Lechaplais C., Louesse C., Muselet D., Magdelenat G., Pateau E., Petit E., Sirvain-Trukniewicz P., Trybou A., Vega-Czarny N., Bataille E., Bluet E., Bordelais I., Dubois M., Dumont C., Guerin T., Haffray S., Hammadi R., Muanga J., Pellouin V., Robert D., Wunderle E., Gauguet G., Roy A., Sainte-Marthe L., Verdier J., Verdier-Discala C., Hillier L.W., Fulton L., McPherson J., Matsuda F., Wilson R., Scarpelli C., Gyapay G., Wincker P., Saurin W., Quetier F., Waterston R., Hood L., Weissenbach J.
Nature 421:601-607(2003) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[2]Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. expand/collapse author list , Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H., Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K., Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D., Hunkapiller M.W., Myers E.W., Venter J.C.
Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"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 cortex and Pancreas.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL512802 Genomic DNA. No translation available.
CH471061 Genomic DNA. Translation: EAW81892.1.
BC003539 mRNA. Translation: AAH03539.1.
BC137495 mRNA. Translation: AAI37496.1.
RefSeqNP_777551.2. NM_174891.3.
UniGeneHs.27183.

3D structure databases

ProteinModelPortalQ96F83.
ModBaseSearch...
MobiDBSearch...

Polymorphism databases

DMDM125863840.

Proteomic databases

PaxDbQ96F83.
PRIDEQ96F83.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000547315; ENSP00000450114; ENSG00000140104.
GeneID122616.
KEGGhsa:122616.
UCSCuc001ypy.1. human.

Organism-specific databases

CTD122616.
GeneCardsGC14P105452.
HGNCHGNC:20126. C14orf79.
HPAHPA042052.
neXtProtNX_Q96F83.
PharmGKBPA134876308.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG43808.
HOGENOMHOG000060102.
HOVERGENHBG081269.
InParanoidQ96F83.
OMAFEGFRES.
PhylomeDBQ96F83.
TreeFamTF335916.

Gene expression databases

ArrayExpressQ96F83.
BgeeQ96F83.
CleanExHS_C14orf79.
GenevestigatorQ96F83.

Family and domain databases

ProtoNetSearch...

Other

GeneWikiC14orf79.
GenomeRNAi122616.
NextBio80929.

Entry information

Entry nameCN079_HUMAN
AccessionPrimary (citable) accession number: Q96F83
Secondary accession number(s): B2RPK9, Q9BTP4
Entry history
Integrated into UniProtKB/Swiss-Prot: February 6, 2007
Last sequence update: February 6, 2007
Last modified: April 16, 2014
This is version 69 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 chromosome 14

Human chromosome 14: entries, gene names and cross-references to MIM