Skip Header

You are using a version of Internet Explorer that may not display all features of this website. Please upgrade to a modern browser.
Contribute Send feedback
Read comments (?) or add your own

C4P0C4 (C4P0C4_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified January 22, 2014. Version 25. 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:DISC1 EMBL ACR40073.1
OrganismHomo sapiens (Human) EMBL ACR40073.1
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length547 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

Sequences

Sequence LengthMass (Da)Tools
C4P0C4 [UniParc].

Last modified July 7, 2009. Version 1.
Checksum: 4F05E7A07D20F09F

FASTA54758,908
        10         20         30         40         50         60 
MPGGGPQGAP AAAGGGGVSH RAGSRDCLPP AACFRRRRLA RRPGYMRSST GPGIGFLSPA 

        70         80         90        100        110        120 
VGTLFRFPGG VSGEESHHSE SRARQCGLDS RGLLVRSPVS KSAAAPTVTS VRGTSAHFGI 

       130        140        150        160        170        180 
QLRGGTRLPD RLSWPCGPGS AGWQQEFAAM DSSETLDASW EAACSDGARR VRAAGSLPSA 

       190        200        210        220        230        240 
ELSSNSCSPG CGPEVPPTPP GSHSAFTSSF SFIRLSLGSA GERGEAEGCP PSREAESHCQ 

       250        260        270        280        290        300 
SPQEMGAKAA SLDGPHEDPR CLSRPFSLLA TRVSADLAQA ARNSSRPERD MHSLPDMDPG 

       310        320        330        340        350        360 
SSSSLDPSLA GCGGDGSSGS GDAHSWDTLL RKWEPVLRDC LLRNRRQMEV ISLRLKLQKL 

       370        380        390        400        410        420 
QEDAVENDDY DKAETLQQRL EDLEQEKISL HFQLPSRQPA LSSFLGHLAA QVQAALRRGA 

       430        440        450        460        470        480 
TQQASGDDTH TPLRMEPRLL EPTAQDSLHV SITRRDWLLQ EKQQLQKEIE ALQARMFVLE 

       490        500        510        520        530        540 
AKDQQLRREI EEQEQQLQWQ GCDLTPLVGQ LSLGQLQEVS KALQDTLASA GQIPFHAEPP 


ETIRRYC 

« Hide

References

[1]"DISC1 splice variants are upregulated in schizophrenia and associated with risk polymorphisms."
Nakata K., Lipska B.L., Hyde T.M., Ye T., Newburn E.N., Morita Y., Vakkalanka R., Barenboim M., Sei Y., Weinberger D.R., Kleinman J.E.
Proc. Natl. Acad. Sci. U.S.A. 106:15873-15878(2009)
Cited for: NUCLEOTIDE SEQUENCE.
[2]"Novel Fetal DISC1 Splice Variants Are Upregulated in Schizophrenia and Associated with Risk Polymorphisms."
Nakata K., Lipska B.K., Hyde T.M., Ye T., Fink E.N., Morita Y., Vakkalanka R., Barenboim M., Sei Y., Weinberger D.R., Kleinman J.E.
Submitted (MAR-2009) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
FJ804207 mRNA. Translation: ACR40073.1.
RefSeqNP_001158021.1. NM_001164549.1.
UniGeneHs.13318.

3D structure databases

ProteinModelPortalC4P0C4.
ModBaseSearch...
MobiDBSearch...

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

GeneID27185.
KEGGhsa:27185.
UCSCuc010pwq.2. human.

Organism-specific databases

CTD27185.
PharmGKBPA27342.

Phylogenomic databases

KOK16534.

Family and domain databases

InterProIPR026081. DISC1.
[Graphical view]
PANTHERPTHR14332. PTHR14332. 1 hit.
ProtoNetSearch...

Other

GenomeRNAi27185.
NextBio50024.

Entry information

Entry nameC4P0C4_HUMAN
AccessionPrimary (citable) accession number: C4P0C4
Entry history
Integrated into UniProtKB/TrEMBL: July 7, 2009
Last sequence update: July 7, 2009
Last modified: January 22, 2014
This is version 25 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.