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Reviewed, UniProtKB/Swiss-Prot P59093 (CU099_HUMAN)

Last modified November 24, 2009. Version 43. 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 · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Uncharacterized protein C21orf99
Alternative name(s):
    Cancer/testis antigen 85
      Short name=CT85
Gene names
Name: C21orf99
OrganismHomo sapiens (Human) [Complete proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length68 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at transcript level.

General annotation (Comments)

Tissue specificity

Expressed in testis, prostate, brain, placenta and trachea. Not expressed in lung, small intestine, breast, heart, uterus, bone marrow, fetal brain, colon, fetal liver, liver, thymus, salivary glands, spinal chord, kidney, spleen, muscle and adrenal gland. Ref.1

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 – 6868Uncharacterized protein C21orf99
PRO_0000079545

Natural variations

Natural variant421T → M: dbSNP rs1054926.
VAR_020956
Natural variant461P → T: dbSNP rs10439727.
VAR_033764

Sequences

Sequence LengthMass (Da)Tools
P59093-1 [UniParc].

Last modified November 15, 2002. Version 1.
Checksum: 937A2497867EBE0B

FASTA688,601
        10         20         30         40         50         60 
MQMQMELISL NAFINNFWNI NKRYLKILKI VIQKEHLKEH LTRLHPWRKE HLTRLKAWWK 


EHLTNRIQ 

« Hide

References

« Hide 'large scale' references
[1]"Nineteen additional unpredicted transcripts from human chromosome 21."
Reymond A., Camargo A.A., Deutsch S., Stevenson B.J., Parmigiani R.B., Ucla C., Bettoni F., Rossier C., Lyle R., Guipponi M., de Souza S., Iseli C., Jongeneel C.V., Bucher P., Simpson A.J.G., Antonarakis S.E.
Genomics 79:824-832(2002) [PubMed: 12036297] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY.
[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].

Cross-references

Sequence databases

AF427490 mRNA. Translation: AAM53529.1.
BC126176 mRNA. Translation: AAI26177.1.
BC126178 mRNA. Translation: AAI26179.1.
IPIIPI00171431.
UniGeneHs.558645
Hs.579474
Hs.653094

3D structure databases

ModBaseSearch...

Genome annotation databases

EnsemblENST00000427291; ENSP00000402236; ENSG00000163046; Homo sapiens. [Genome view]

Organism-specific databases

GeneCardsGC21P013332.
HGNCHGNC:16620. C21orf99.
PharmGKBPA134962599.
GenAtlasSearch...

Phylogenomic databases

HOVERGENP59093.

Gene expression databases

CleanExHS_C21orf99.
GenevestigatorP59093.
GermOnlineENSG00000155258. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Entry information

Entry nameCU099_HUMAN
AccessionPrimary (citable) accession number: P59093
Secondary accession number(s): A0AV18
Entry history
Integrated into UniProtKB/Swiss-Prot: November 15, 2002
Last sequence update: November 15, 2002
Last modified: November 24, 2009
This is version 43 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 21

Human chromosome 21: 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 · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents