Q9UPB4 (Q9UPB4_HUMAN) Unreviewed, UniProtKB/TrEMBL

Names and origin

Protein names

Submitted name:
Dystrophin EMBL AAD03809.1

Gene names

Name:

DMD EMBL AAD03809.1

Organism

Homo sapiens (Human) EMBL AAD03809.1

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	52 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 AAD03809.1
	Non-terminal residue	52	1	EMBL AAD03809.1

Sequences

	Sequence		Length	Mass (Da)
	Q9UPB4 [UniParc]. Last modified May 1, 2000. Version 1. Checksum: 0E8A2DF471E6152C	FASTA	52	5,942
	10 20 30 40 50 LLVSDIQTIQ PSLNSVNEGG QKIKNEAEPE FASRLETELK ELNTQWDHMC QQ

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	AF047505 Genomic DNA. Translation: AAD03809.1.
IPI	IPI00375141.
UniGene	Hs.495912.
3D structure databases
ModBase	Search...
Protein-protein interaction databases
STRING	Q9UPB4.
Proteomic databases
PRIDE	Q9UPB4.
Protocols and materials databases
StructuralBiologyKnowledgebase	Search...
Gene expression databases
ArrayExpress	Q9UPB4.
Bgee	Q9UPB4.
Family and domain databases
InterPro	IPR002017. Spectrin_repeat. [Graphical view]
Pfam	PF00435. Spectrin. 1 hit. [Graphical view]
ProtoNet	Search...
Other
ChiTaRS	DMD. human.

Entry information

Entry name

Q9UPB4_HUMAN

Accession

Primary (citable) accession number: Q9UPB4

Entry history

Integrated into UniProtKB/TrEMBL:	May 1, 2000
Last sequence update:	May 1, 2000
Last modified:	April 3, 2013
This is version 41 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.