Q9UPB5 (Q9UPB5_HUMAN) Unreviewed, UniProtKB/TrEMBL

Names and origin

Protein names

Submitted name:
Dystrophin EMBL AAD03808.1

Gene names

Name:

DMD EMBL AAD03808.1

Organism

Homo sapiens (Human) EMBL AAD03808.1

Taxonomic identifier

9606 [NCBI]

Taxonomic lineage

cellular organisms › Eukaryota › Opisthokonta › Metazoa › Eumetazoa › Bilateria › Deuterostomia › Chordata › Craniata › Vertebrata › Gnathostomata › Teleostomi › Euteleostomi › Sarcopterygii › Tetrapoda › Amniota › Mammalia › Theria › Eutheria › Euarchontoglires › Primates › Haplorrhini › Simiiformes › Catarrhini › Hominoidea › Hominidae › Homininae › Homo

Protein attributes

Sequence length	36 AA.
Sequence status	Fragment.
Protein existence	Evidence at transcript level

Ontologies

Gene Ontology (GO)
Biological_process	establishment of blood-nerve barrier Inferred from electronic annotation. Source: Compara establishment of glial blood-brain barrier Inferred from electronic annotation. Source: Compara muscle cell homeostasis Inferred from electronic annotation. Source: Compara muscle fiber development Inferred from electronic annotation. Source: Compara myotube cell development Inferred from electronic annotation. Source: Compara neurotransmitter receptor metabolic process Inferred from electronic annotation. Source: Compara nucleus localization Inferred from electronic annotation. Source: Compara olfactory nerve structural organization Inferred from electronic annotation. Source: Compara regulation of transcription, DNA-dependent Inferred from electronic annotation. Source: Compara
Cellular_component	Z disc Inferred from electronic annotation. Source: Compara cell-substrate junction Inferred from electronic annotation. Source: Compara dystrophin-associated glycoprotein complex Inferred from electronic annotation. Source: Compara membrane raft Inferred from electronic annotation. Source: Compara neuron projection terminus Inferred from electronic annotation. Source: Compara sarcolemma Inferred from electronic annotation. Source: Compara synapse Inferred from electronic annotation. Source: Compara
Complete GO annotation...

Sequence annotation (Features)

	Feature key	Position(s)	Length	Description	Graphical view	Feature identifier
Experimental info
	Non-terminal residue	1	1	EMBL AAD03808.1
	Non-terminal residue	36	1	EMBL AAD03808.1

Sequences

	Sequence		Length	Mass (Da)
	Q9UPB5 [UniParc]. Last modified May 1, 2000. Version 1. Checksum: D1960AB38174D2E5	FASTA	36	4,084
	10 20 30 CLFSAWLSEK EDAVNKIHTT GFKDQNEMLS SLQKLA

References

[1]	"Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene." McNaughton J.C., Cockburn D.J., Hughes G., Jones W.A., Laing N.G., Ray P.N., Stockwell P.A., Petersen G.B. Gene 222:41-51(1998) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE.
[2]	McNaughton J. Submitted (FEB-1998) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE.
+	Additional computationally mapped references.

Cross-references

Sequence databases
EMBL GenBank DDBJ	AF047502 Genomic DNA. Translation: AAD03808.1.
IPI	IPI00304639.
UniGene	Hs.495912.
3D structure databases
ModBase	Search...
Protein-protein interaction databases
STRING	Q9UPB5.
Proteomic databases
PRIDE	Q9UPB5.
Protocols and materials databases
StructuralBiologyKnowledgebase	Search...
Gene expression databases
ArrayExpress	Q9UPB5.
Bgee	Q9UPB5.
Family and domain databases
ProtoNet	Search...
Other
ChiTaRS	DMD. human.

Entry information

Entry name

Q9UPB5_HUMAN

Accession

Primary (citable) accession number: Q9UPB5

Entry history

Integrated into UniProtKB/TrEMBL:	May 1, 2000
Last sequence update:	May 1, 2000
Last modified:	April 3, 2013
This is version 39 of the entry and version 1 of the sequence. [Complete history]

Entry status

Unreviewed (UniProtKB/TrEMBL)

Disclaimer

Any 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.