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Reviewed, UniProtKB/Swiss-Prot Q7L3V2 (CV029_HUMAN)

Last modified December 15, 2009. Version 33. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (3) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Uncharacterized protein C22orf29
Gene names
Name: C22orf29
OrganismHomo sapiens (Human) [Complete proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length364 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at transcript level.

Ontologies

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

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 364364Uncharacterized protein C22orf29
PRO_0000295910

Regions

Compositional bias265 – 32460Pro-rich

Natural variations

Natural variant1161R → H: dbSNP rs17745302.
VAR_034590
Natural variant1231D → Y: dbSNP rs34027839. Ref.1
VAR_034591

Experimental info

Sequence conflict2061A → V in CAE45984. Ref.1
Sequence conflict2061A → V in CAE46001. Ref.1

Sequences

Sequence LengthMass (Da)Tools
Q7L3V2-1 [UniParc].

Last modified May 24, 2005. Version 1.
Checksum: 28FD406757BE082A

FASTA36439,299
        10         20         30         40         50         60 
MPRGRCRQQG PRIPIWAAAN YANAHPWQQM DKASPGVAYT PLVDPWIERP CCGDTVCVRT 

        70         80         90        100        110        120 
TMEQKSTASG TCGGKPAERG PLAGHMPSSR PHRVDFCWVP GSDPGTFDGS PWLLDRFLAQ 

       130        140        150        160        170        180 
LGDYMSFHFE HYQDNISRVC EILRRLTGRA QAWAAPYLDG DLPLPDDYEL FCQDLKEVVQ 

       190        200        210        220        230        240 
DPNSFAEYHA VVTCPLPLAS SQLPVAPQLP VVRQYLARFL EGLALDMGTA PRSLPAAMAT 

       250        260        270        280        290        300 
PAVSGSNSVS RSALFEQQLT KESTPGPKEP PVLPSSTCSS KPGPVEPASS QPEEAAPTPV 

       310        320        330        340        350        360 
PRLSESANPP AQRPDPAHPG GPKPQKTEEE VLETEGDQEV SLGTPQEVVE APETPGEPPL 


SPGF 

« Hide

References

[1]"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], VARIANT TYR-123.
Tissue: Endometrial tumor and Uterine endothelium.
[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: Uterus.
[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 39-364.

Cross-references

Sequence databases

BX640785 mRNA. Translation: CAE45875.1.
BX640969 mRNA. Translation: CAE45984.1.
BX640998 mRNA. Translation: CAE46001.1.
BC011679 mRNA. Translation: AAH11679.2.
AK024778 mRNA. Translation: BAB14998.1. Different initiation.
IPIIPI00472049.
RefSeqNP_078903.3.
UniGeneHs.105642

3D structure databases

ModBaseSearch...

Protein-protein interaction databases

STRINGQ7L3V2.

Proteomic databases

PRIDEQ7L3V2.

Genome annotation databases

EnsemblENST00000328554; ENSP00000330596; ENSG00000215012; Homo sapiens. [Genome view]
ENST00000405640; ENSP00000384924; ENSG00000215012; Homo sapiens. [Genome view]
ENST00000407472; ENSP00000386111; ENSG00000215012; Homo sapiens. [Genome view]
GeneID79680.
KEGGhsa:79680.
UCSCuc002zqg.1. human.

Organism-specific databases

CTD79680.
GeneCardsGC22M018213.
HGNCHGNC:26112. C22orf29.
HPAHPA000721.
HPA001419.
GenAtlasSearch...

Phylogenomic databases

HOVERGENQ7L3V2.
InParanoidQ7L3V2.
OMASTASGTC.
OrthoDBEOG9M94CH.

Gene expression databases

BgeeQ7L3V2.
GenevestigatorQ7L3V2.

Family and domain databases

ProtoNetSearch...

Other Resources

NextBio68930.

Entry information

Entry nameCV029_HUMAN
AccessionPrimary (citable) accession number: Q7L3V2
Secondary accession number(s): Q6MZM8, Q6N000, Q9H7A0
Entry history
Integrated into UniProtKB/Swiss-Prot: July 24, 2007
Last sequence update: May 24, 2005
Last modified: December 15, 2009
This is version 33 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)
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 22

Human chromosome 22: 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

Names and origin · Protein attributes · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents