Q12925 (Q12925_HUMAN) Unreviewed, UniProtKB/TrEMBL

Names and origin

Protein names	Submitted name: Putative uncharacterized protein EMBL AAA62165.1
Organism	Homo sapiens (Human) EMBL AAA62165.1
Taxonomic identifier	9606 [NCBI]
Taxonomic lineage	Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo

Protein attributes

Sequence length	113 AA.
Sequence status	Fragment.
Protein existence	Evidence at transcript level

Sequence annotation (Features)

	Feature key	Position(s)	Length	Description	Graphical view	Feature identifier
Experimental info
	Non-terminal residue	113	1	EMBL AAA62165.1

Sequences

	Sequence		Length	Mass (Da)
	Q12925 [UniParc]. Last modified November 1, 1996. Version 1. Checksum: F93B6A01C558A7B2	FASTA	113	11,385
	10 20 30 40 50 60 MEPASAHLLL NDMIAGQHCL EVTIFICFST SFCSSFSFSA SSSISLTLDS SASGPQWRVP 70 80 90 100 110 VTSTSPAPPP PLGCRGSRTS PGPGAPGGRG AGAAPLRARA PARAPAARPQ APP

References

[1]	"Cloning, sequencing, and chromosomal assignment of a new cDNA clone to Xq12-q13 and 14q11." Lamartine J., Wang Q., Kaneko K., Tsuji S., Mattei M., Lenoir G., Sylla B.S. Submitted (JUL-1994) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE.
+	Additional computationally mapped references.

Cross-references

Sequence databases
EMBL GenBank DDBJ	U12206 mRNA. Translation: AAA62165.1.
IPI	IPI00030249.
UniGene	Hs.707712.
3D structure databases
ModBase	Search...
Proteomic databases
PRIDE	Q12925.
Protocols and materials databases
StructuralBiologyKnowledgebase	Search...
Family and domain databases
ProtoNet	Search...

Entry information

Entry name

Q12925_HUMAN

Accession

Primary (citable) accession number: Q12925

Entry history

Integrated into UniProtKB/TrEMBL:	November 1, 1996
Last sequence update:	November 1, 1996
Last modified:	March 2, 2010
This is version 33 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.