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Q96TC6 (Q96TC6_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified January 22, 2014. Version 23. Feed History...

Clusters with 100%, 90%, 50% identity | Third-party data text xml rdf/xml gff fasta
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Names and origin

Protein names
Gene names
Name:hucep-13 EMBL BAB46926.1
OrganismHomo sapiens (Human) EMBL BAB46926.1
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length162 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

Sequences

Sequence LengthMass (Da)Tools
Q96TC6 [UniParc].

Last modified December 1, 2001. Version 1.
Checksum: 56D06D0E6B849587

FASTA16216,555
        10         20         30         40         50         60 
MGGTRPHSFH RALRPDTADQ PHSAQEAASG VGAQRGTAAS STAGCGAAGP GPSAWAAEYI 

        70         80         90        100        110        120 
FYLSETSIFL GSNPTCHHVD ISSYLTMLSL LGAVLVGPGP CIMPRSQLQG PSWGPGWALG 

       130        140        150        160 
SGPCCSSPSH QPVPVVRKPG LLSSFLLGEC QTQGPSTGLG WE 

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References

[1]"Cloning of a gene expressed in human cerebral cortex."
Yoshimoto M., Yazaki M., Matsumoto K., Takayama K., Tsuritani K.
Submitted (MAR-1997) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AB002534 mRNA. Translation: BAB46926.1.
UniGeneHs.106674.

3D structure databases

ModBaseSearch...
MobiDBSearch...

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Family and domain databases

ProtoNetSearch...

Entry information

Entry nameQ96TC6_HUMAN
AccessionPrimary (citable) accession number: Q96TC6
Entry history
Integrated into UniProtKB/TrEMBL: December 1, 2001
Last sequence update: December 1, 2001
Last modified: January 22, 2014
This is version 23 of the entry and version 1 of the sequence. [Complete history]
Entry statusUnreviewed (UniProtKB/TrEMBL)
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.