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F2WSI7 (F2WSI7_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified May 1, 2013. Version 9. 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:DMD EMBL ADZ31226.1
OrganismHomo sapiens (Human) EMBL ADZ31226.1
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length19 AA.
Sequence statusFragment.
Protein existenceEvidence at transcript level

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Experimental info

Non-terminal residue11 EMBL ADZ31226.1
Non-terminal residue191 EMBL ADZ31226.1

Sequences

Sequence LengthMass (Da)Tools
F2WSI7 [UniParc].

Last modified May 31, 2011. Version 1.
Checksum: 80419F232D91BA10

FASTA192,205
        10 
SVQGPWERAI SPNKVPYYI 

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References

[1]"Detection of a novel variant of dystrophin gene [intron 61 del cag] in a Chinese family."
Mo G., Hu Z., Yu C., Zhan Y., Zhu Q.
Submitted (SEP-2010) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE.
Tissue: Blood EMBL ADZ31226.1.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
HQ237465 Genomic DNA. Translation: ADZ31226.1.
IPIIPI00376375.

3D structure databases

ModBaseSearch...

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Gene expression databases

ArrayExpressF2WSI7.
BgeeF2WSI7.

Family and domain databases

ProtoNetSearch...

Other

ChiTaRSDMD. human.
NextBio35505847.

Entry information

Entry nameF2WSI7_HUMAN
AccessionPrimary (citable) accession number: F2WSI7
Entry history
Integrated into UniProtKB/TrEMBL: May 31, 2011
Last sequence update: May 31, 2011
Last modified: May 1, 2013
This is version 9 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.