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Reviewed, UniProtKB/Swiss-Prot P59092 (CU094_HUMAN)

Last modified November 24, 2009. Version 42. 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 C21orf94
Gene names
Name: C21orf94
OrganismHomo sapiens (Human) [Complete proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length62 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at transcript level.

General annotation (Comments)

Tissue specificity

Expressed in testis, prostate, fetal brain, brain, uterus, bone marrow, placenta, colon, fetal liver, thymus, salivary glands, spinal chord, muscle, trachea and adrenal gland. Not expressed in lung, small intestine, breast, heart, liver, kidney and spleen. 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 – 6262Uncharacterized protein C21orf94
PRO_0000079542

Natural variations

Natural variant491C → Y: dbSNP rs2831368.
VAR_020098

Sequences

Sequence LengthMass (Da)Tools
P59092-1 [UniParc].

Last modified November 15, 2002. Version 1.
Checksum: 8877D5B333B9CA66

FASTA627,260
        10         20         30         40         50         60 
MLKIAVMEVS QSAWKTVWKE VAWPHCHVPL SLKKGHICLC ARQHIHLVCV YTLVYVFCYL 


TF 

« 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

AF427489 mRNA. Translation: AAM53528.1.
BC126226 mRNA. Translation: AAI26227.1.
BC126230 mRNA. Translation: AAI26231.1.
IPIIPI00171430.
UniGeneHs.505079

3D structure databases

ModBaseSearch...

Proteomic databases

PRIDEP59092.

Organism-specific databases

GeneCardsGC21P028309.
HGNCHGNC:16622. C21orf94.
PharmGKBPA38408.
GenAtlasSearch...

Phylogenomic databases

HOGENOMP59092.

Gene expression databases

CleanExHS_C21orf94.
GenevestigatorP59092.
GermOnlineENSG00000178457. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Entry information

Entry nameCU094_HUMAN
AccessionPrimary (citable) accession number: P59092
Secondary accession number(s): A0AV62
Entry history
Integrated into UniProtKB/Swiss-Prot: November 15, 2002
Last sequence update: November 15, 2002
Last modified: November 24, 2009
This is version 42 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