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Q7Z7L8 (CK096_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 47. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (3) | 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:
Uncharacterized protein C11orf96
Alternative name(s):
Protein Ag2 homolog
Gene names
Name:C11orf96
Synonyms:AG2
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length435 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Post-translational modification

Phosphorylated upon DNA damage, probably by ATM or ATR. Ref.3

Ontologies

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

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 435435Uncharacterized protein C11orf96
PRO_0000320641

Regions

Compositional bias242 – 30766Pro-rich

Amino acid modifications

Modified residue3681Phosphothreonine Ref.3
Modified residue3851Phosphoserine Ref.3
Modified residue4071Phosphothreonine By similarity

Natural variations

Natural variant261T → A.
Corresponds to variant rs1973717 [ dbSNP | Ensembl ].
VAR_039242
Natural variant471S → P.
Corresponds to variant rs12797684 [ dbSNP | Ensembl ].
VAR_039243
Natural variant1101R → S.
Corresponds to variant rs12796438 [ dbSNP | Ensembl ].
VAR_039244
Natural variant1441R → C.
Corresponds to variant rs12796667 [ dbSNP | Ensembl ].
VAR_039245
Natural variant1511F → S.
Corresponds to variant rs12798337 [ dbSNP | Ensembl ].
VAR_039246
Natural variant3521P → S.
Corresponds to variant rs2434483 [ dbSNP | Ensembl ].
VAR_039247

Sequences

Sequence LengthMass (Da)Tools
Q7Z7L8 [UniParc].

Last modified May 5, 2009. Version 3.
Checksum: F536980973B14478

FASTA43546,114
        10         20         30         40         50         60 
MGNKQPQKVT VPTGTALQGV VLIVSTLHQP GGWICGKDPC CSLRPLSNSV QNALACKSKQ 

        70         80         90        100        110        120 
DYQAGILFKT RAFISRDCGS DAAEDSASKG ETYTLTLEHK GAGEGDLRPR GQPGWCRLGD 

       130        140        150        160        170        180 
PRRDSARPVA AIEGPCPGAA RASRVLRGRG FSRNPRGRGL PSGAGWRGAG GAGEGAVTFP 

       190        200        210        220        230        240 
ERRGDVRRKG AGRARFKWHS LSSELRAVWA AAGYISREPG RRGADGDSSG GERLGARRNS 

       250        260        270        280        290        300 
APRAPCPPTG PPARPPSRGA PARAREGRRH PAADLDPPPG EPPAAASRGA PAQRPPSESP 

       310        320        330        340        350        360 
GAPPPGPADA GGAMAAKPGE LMGICSSYQA VMPHFVCLAD EFPQPVRPAK LPKGRGRLRR 

       370        380        390        400        410        420 
PRQSRFKTQP VTFDEIQEVE EEGVSPMEEE KAKKSFLQSL ECLRRSTQSL SLQREQLSSC 

       430 
KLRNSLDSSD SDSAL 

« Hide

References

[1]"Human chromosome 11 DNA sequence and analysis including novel gene identification."
Taylor T.D., Noguchi H., Totoki Y., Toyoda A., Kuroki Y., Dewar K., Lloyd C., Itoh T., Takeda T., Kim D.-W., She X., Barlow K.F., Bloom T., Bruford E., Chang J.L., Cuomo C.A., Eichler E., FitzGerald M.G. expand/collapse author list , Jaffe D.B., LaButti K., Nicol R., Park H.-S., Seaman C., Sougnez C., Yang X., Zimmer A.R., Zody M.C., Birren B.W., Nusbaum C., Fujiyama A., Hattori M., Rogers J., Lander E.S., Sakaki Y.
Nature 440:497-500(2006) [PubMed: 16554811] [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] OF 209-435.
Tissue: Salivary gland.
[3]"ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage."
Matsuoka S., Ballif B.A., Smogorzewska A., McDonald E.R. III, Hurov K.E., Luo J., Bakalarski C.E., Zhao Z., Solimini N., Lerenthal Y., Shiloh Y., Gygi S.P., Elledge S.J.
Science 316:1160-1166(2007) [PubMed: 17525332] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT THR-368 AND SER-385, MASS SPECTROMETRY.
Tissue: Embryonic kidney.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AC087521 Genomic DNA. No translation available.
BC052560 mRNA. Translation: AAH52560.1.
IPIIPI00398347.
RefSeqNP_001138505.1. NM_001145033.1.
UniGeneHs.714890.

3D structure databases

ProteinModelPortalQ7Z7L8.
ModBaseSearch...

PTM databases

PhosphoSiteQ7Z7L8.

Polymorphism databases

DMDM229463005.

Proteomic databases

PRIDEQ7Z7L8.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000339446; ENSP00000340667; ENSG00000187479.
GeneID387763.
KEGGhsa:387763.

Organism-specific databases

CTD387763.
GeneCardsGC11P043947.
H-InvDBHIX0035967.
HGNCHGNC:38675. C11orf96.
HPAHPA038843.
neXtProtNX_Q7Z7L8.
PharmGKBPA165543281.
GenAtlasSearch...

Phylogenomic databases

eggNOGmaNOG22857.
GeneTreeENSGT00390000016821.
InParanoidQ7Z7L8.
OMAGEGAVTF.
OrthoDBEOG4SJ5FG.

Gene expression databases

ArrayExpressQ7Z7L8.
BgeeQ7Z7L8.
GenevestigatorQ7Z7L8.

Family and domain databases

ProtoNetSearch...

Entry information

Entry nameCK096_HUMAN
AccessionPrimary (citable) accession number: Q7Z7L8
Entry history
Integrated into UniProtKB/Swiss-Prot: February 26, 2008
Last sequence update: May 5, 2009
Last modified: January 25, 2012
This is version 47 of the entry and version 3 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 11

Human chromosome 11: 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