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Q8N655 (CJ012_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 67. 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 C10orf12
Gene names
Name:C10orf12
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length1247 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Post-translational modification

Phosphorylated upon DNA damage, probably by ATM or ATR. Ref.5 Ref.6 Ref.7 Ref.8 Ref.9

Sequence caution

The sequence BAB14396.1 differs from that shown. Reason: Erroneous initiation.

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 – 12471247Uncharacterized protein C10orf12
PRO_0000089783

Amino acid modifications

Modified residue2731Phosphoserine Ref.7 Ref.9
Modified residue4281Phosphothreonine Ref.5
Modified residue4491Phosphoserine Ref.8
Modified residue4511Phosphothreonine Ref.8
Modified residue7671Phosphoserine Ref.9
Modified residue9931Phosphothreonine Ref.7
Modified residue9961Phosphoserine Ref.7
Modified residue10771Phosphoserine Ref.6
Modified residue11211Phosphothreonine Ref.6

Natural variations

Natural variant491N → S.
Corresponds to variant rs11188980 [ dbSNP | Ensembl ].
VAR_033687
Natural variant3141L → P.
Corresponds to variant rs7082522 [ dbSNP | Ensembl ].
VAR_033688
Natural variant3961E → G.
Corresponds to variant rs35128733 [ dbSNP | Ensembl ].
VAR_050846
Natural variant4011P → A.
Corresponds to variant rs34104025 [ dbSNP | Ensembl ].
VAR_033689
Natural variant5351I → L.
Corresponds to variant rs3829856 [ dbSNP | Ensembl ].
VAR_033690
Natural variant5561T → P.
Corresponds to variant rs7894200 [ dbSNP | Ensembl ].
VAR_050847
Natural variant5791N → S.
Corresponds to variant rs7894315 [ dbSNP | Ensembl ].
VAR_059605
Natural variant6141R → G.
Corresponds to variant rs7894545 [ dbSNP | Ensembl ].
VAR_059606
Natural variant7161A → P.
Corresponds to variant rs7895159 [ dbSNP | Ensembl ].
VAR_059607

Experimental info

Sequence conflict6121E → G in BAB14396. Ref.3
Sequence conflict8991D → G in BAB14396. Ref.3

Sequences

Sequence LengthMass (Da)Tools
Q8N655 [UniParc].

Last modified October 1, 2002. Version 1.
Checksum: 8D54C9ACE489CEE8

FASTA1,247137,223
        10         20         30         40         50         60 
MQSSALVESL ITVKMAAENS EEGNTCIIPQ RNLFKALSEE AWNSGFMGNS SRTADKENTL 

        70         80         90        100        110        120 
QCPKTPLRQD LEANEQDARP KQENHLHSLG RNKVGYHLHP SDKGQFDHSK DGWLGPGPMP 

       130        140        150        160        170        180 
AVHKAANGHS RTKMISTSIK TARKSKRASG LRINDYDNQC DVVYISQPIT ECHFENQKSI 

       190        200        210        220        230        240 
LSSRKTARKS TRGYFFNGDC CELPTVRTLA RNLHSQEKAS CSALASEAVF TPKQTLTIPA 

       250        260        270        280        290        300 
PRHTVDVQLP REDNPEEPSK EITSHEEGGG DVSPRKEPQE PEVCPTKIKP NLSSSPRSEE 

       310        320        330        340        350        360 
TTASSLVWPL PAHLPEEDLP EGGSTVSAPT ASGMSSPEHN QPPVALLDTE EMSVPQDCHL 

       370        380        390        400        410        420 
LPSTESFSGG VSEDVISRPH SPPEIVSREE SPQCSENQSS PMGLEPPMSL GKAEDNQSIS 

       430        440        450        460        470        480 
AEVESGDTQE LNVDPLLKES STFTDENPSE TEESEAAGGI GKLEGEDGDV KCLSEKDTYD 

       490        500        510        520        530        540 
TSIDSLEENL DKKKKGKKFP EASDRCLRSQ LSDSSSADRC LRNQSSDSSS ACLEIKVPKN 

       550        560        570        580        590        600 
PSAKRSKKEG HPGGTTPKGL LPDSFHTETL EDTEKPSVNE RPSEKDAEQE GEGGGIITRQ 

       610        620        630        640        650        660 
TLKNMLDKEV KELRGEIFPS RDPITTAGQP LPGERLEIYV QSKMDEKNAH IPSESIACKR 

       670        680        690        700        710        720 
DPEQAKEEPG HIPTQHVEEA VNEVDNENTQ QKDDESDAPC SSLGLSSSGS GDAARAPKSV 

       730        740        750        760        770        780 
PRPKRLTSST YNLRHAHSLG SLDASKVTSE KEAAQVNPIM PKENGASESG DPLDEDDVDT 

       790        800        810        820        830        840 
VVDEQPKFME WCAEEENQEL IANFNAQYMK VQKGWIQLEK EGQPTPRARN KSDKLKEIWK 

       850        860        870        880        890        900 
SKKRSRKCRS SLESQKCSPV QMLFMTNFKL SNVCKWFLET TETRSLVIVK KLNTRLPGDV 

       910        920        930        940        950        960 
PPVKHPLQKY APSSLYPSSL QAERLKKHLK KFPGATPAKN NWKMQKLWAK FRENPDQVEP 

       970        980        990       1000       1010       1020 
EDGSDVSPGP NSEDSIEEVK EDRNSHPPAN LPTPASTRIL RKYSNIRGKL RAQQRLIKNE 

      1030       1040       1050       1060       1070       1080 
KMECPDALAV ESKPSRKSVC INPLMSPKLA LQVDADGFPV KPKSTEGMKG RKGKQVSEIL 

      1090       1100       1110       1120       1130       1140 
PKAEVQSKRK RTEGSSPPDS KNKGPTVKAS KEKHADGATK TPAAKRPAAR DRSSQPPKKT 

      1150       1160       1170       1180       1190       1200 
SLKENKVKIP KKSAGKSCPP SRKEKENTNK RPSQSIASET LTKPAKQKGA GESSSRPQKA 

      1210       1220       1230       1240 
TNRKQSSGKT RARPSTKTPE SSAAQRKRKL KAKLDCSHSK RRRLDAK 

« Hide

References

[1]"The DNA sequence and comparative analysis of human chromosome 10."
Deloukas P., Earthrowl M.E., Grafham D.V., Rubenfield M., French L., Steward C.A., Sims S.K., Jones M.C., Searle S., Scott C., Howe K., Hunt S.E., Andrews T.D., Gilbert J.G.R., Swarbreck D., Ashurst J.L., Taylor A., Battles J. expand/collapse author list , Bird C.P., Ainscough R., Almeida J.P., Ashwell R.I.S., Ambrose K.D., Babbage A.K., Bagguley C.L., Bailey J., Banerjee R., Bates K., Beasley H., Bray-Allen S., Brown A.J., Brown J.Y., Burford D.C., Burrill W., Burton J., Cahill P., Camire D., Carter N.P., Chapman J.C., Clark S.Y., Clarke G., Clee C.M., Clegg S., Corby N., Coulson A., Dhami P., Dutta I., Dunn M., Faulkner L., Frankish A., Frankland J.A., Garner P., Garnett J., Gribble S., Griffiths C., Grocock R., Gustafson E., Hammond S., Harley J.L., Hart E., Heath P.D., Ho T.P., Hopkins B., Horne J., Howden P.J., Huckle E., Hynds C., Johnson C., Johnson D., Kana A., Kay M., Kimberley A.M., Kershaw J.K., Kokkinaki M., Laird G.K., Lawlor S., Lee H.M., Leongamornlert D.A., Laird G., Lloyd C., Lloyd D.M., Loveland J., Lovell J., McLaren S., McLay K.E., McMurray A., Mashreghi-Mohammadi M., Matthews L., Milne S., Nickerson T., Nguyen M., Overton-Larty E., Palmer S.A., Pearce A.V., Peck A.I., Pelan S., Phillimore B., Porter K., Rice C.M., Rogosin A., Ross M.T., Sarafidou T., Sehra H.K., Shownkeen R., Skuce C.D., Smith M., Standring L., Sycamore N., Tester J., Thorpe A., Torcasso W., Tracey A., Tromans A., Tsolas J., Wall M., Walsh J., Wang H., Weinstock K., West A.P., Willey D.L., Whitehead S.L., Wilming L., Wray P.W., Young L., Chen Y., Lovering R.C., Moschonas N.K., Siebert R., Fechtel K., Bentley D., Durbin R.M., Hubbard T., Doucette-Stamm L., Beck S., Smith D.R., Rogers J.
Nature 429:375-381(2004) [PubMed: 15164054] [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: Pancreas.
[3]"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. expand/collapse author list , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 236-1247.
[4]"The full-ORF clone resource of the German cDNA consortium."
Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H., Heubner D., Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A., Wiemann S., Schupp I.
BMC Genomics 8:399-399(2007) [PubMed: 17974005] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 1025-1247.
Tissue: Brain.
[5]"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-428, MASS SPECTROMETRY.
Tissue: Embryonic kidney.
[6]"Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle."
Daub H., Olsen J.V., Bairlein M., Gnad F., Oppermann F.S., Korner R., Greff Z., Keri G., Stemmann O., Mann M.
Mol. Cell 31:438-448(2008) [PubMed: 18691976] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-1077 AND THR-1121, MASS SPECTROMETRY.
Tissue: Cervix carcinoma.
[7]"A quantitative atlas of mitotic phosphorylation."
Dephoure N., Zhou C., Villen J., Beausoleil S.A., Bakalarski C.E., Elledge S.J., Gygi S.P.
Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008) [PubMed: 18669648] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-273; THR-993 AND SER-996, MASS SPECTROMETRY.
Tissue: Cervix carcinoma.
[8]"Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach."
Gauci S., Helbig A.O., Slijper M., Krijgsveld J., Heck A.J., Mohammed S.
Anal. Chem. 81:4493-4501(2009) [PubMed: 19413330] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-449 AND THR-451, MASS SPECTROMETRY.
Tissue: Embryonic kidney.
[9]"Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions."
Mayya V., Lundgren D.H., Hwang S.-I., Rezaul K., Wu L., Eng J.K., Rodionov V., Han D.K.
Sci. Signal. 2:RA46-RA46(2009) [PubMed: 19690332] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-273 AND SER-767, MASS SPECTROMETRY.
Tissue: Leukemic T-cell.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL442123 Genomic DNA. Translation: CAH70916.1.
BC024315 mRNA. Translation: AAH24315.1.
AK023084 mRNA. Translation: BAB14396.1. Different initiation.
AL049938 mRNA. Translation: CAB43214.1.
IPIIPI00166933.
PIRT08672.
RefSeqNP_056467.2. NM_015652.2.
UniGeneHs.14555.
Hs.427927.

3D structure databases

ProteinModelPortalQ8N655.
ModBaseSearch...

Protein-protein interaction databases

IntActQ8N655. 2 interactions.
MINTMINT-1484880.

PTM databases

PhosphoSiteQ8N655.

Polymorphism databases

DMDM68565212.

Proteomic databases

PRIDEQ8N655.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000286067; ENSP00000286067; ENSG00000155640.
GeneID26148.
KEGGhsa:26148.
UCSCuc001kmv.1. human.

Organism-specific databases

CTD26148.
GeneCardsGC10P098731.
HGNCHGNC:23420. C10orf12.
HPAHPA038954.
neXtProtNX_Q8N655.
PharmGKBPA134866687.
GenAtlasSearch...

Phylogenomic databases

GeneTreeENSGT00530000064232.
HOVERGENHBG081176.
InParanoidQ8N655.
OMACINPLMS.
OrthoDBEOG42JNQN.
PhylomeDBQ8N655.

Gene expression databases

ArrayExpressQ8N655.
BgeeQ8N655.
CleanExHS_C10orf12.
GenevestigatorQ8N655.
GermOnlineENSG00000155640. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other

NextBio48211.

Entry information

Entry nameCJ012_HUMAN
AccessionPrimary (citable) accession number: Q8N655
Secondary accession number(s): Q9H945, Q9Y457
Entry history
Integrated into UniProtKB/Swiss-Prot: July 5, 2005
Last sequence update: October 1, 2002
Last modified: January 25, 2012
This is version 67 of the entry and version 1 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 10

Human chromosome 10: 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