Skip Header

Contribute Send feedback
Read comments (?) or add your own

Q8NEU1 (Q8NEU1_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified March 2, 2010. Version 23. Feed History...

Clusters with 100%, 90%, 50% identity | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·Sequences·References·Cross-refs·Entry infoCustomize order

Names and origin

Protein names
Gene names
Name:TTL/TEL fusion EMBL AAM97782.1
OrganismHomo sapiens (Human) EMBL AAM97782.1
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length24 AA.
Sequence statusComplete.
Protein existencePredicted

Sequences

Sequence LengthMass (Da)Tools
Q8NEU1 [UniParc].

Last modified October 1, 2002. Version 1.
Checksum: C2DBCE140554DED2

FASTA242,690
        10         20 
MSEDCFRKSG LLLGNVPQLL VIQE 

« Hide

References

[1]"Identification of a Novel Fusion Gene, TTL, Fused to TEL, in Acute Lymphoblastic Leukemia with t(12;13)(p13;q14) and Its Implication in Leukemogenesis."
Qiao Y., Ogawa S., Hangaishi A., Yuji K., Izutsu K., Kunisato A., Imai Y., Wang L., Hosoya N., Sato Y., Nakamura Y., Mitani K., Hirai H.
Submitted (MAY-2002) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE.
Tissue: Brain EMBL AAM97782.1.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AY116216 mRNA. Translation: AAM97782.1.
UniGeneHs.287664.

3D structure databases

ModBaseSearch...

Proteomic databases

PRIDEQ8NEU1.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Family and domain databases

ProtoNetSearch...

Entry information

Entry nameQ8NEU1_HUMAN
AccessionPrimary (citable) accession number: Q8NEU1
Entry history
Integrated into UniProtKB/TrEMBL: October 1, 2002
Last sequence update: October 1, 2002
Last modified: March 2, 2010
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.