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Protein

Uncharacterized protein C10orf25

Gene

C10orf25

Organism
Homo sapiens (Human)
Status
Reviewed-Annotation score: Annotation score: 2 out of 5-Experimental evidence at transcript leveli

Names & Taxonomyi

Protein namesi
Recommended name:
Uncharacterized protein C10orf25
Gene namesi
OrganismiHomo sapiens (Human)
Taxonomic identifieri9606 [NCBI]
Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
Proteomesi
  • UP000005640 Componenti: Unplaced

Organism-specific databases

HGNCiHGNC:23509. C10orf25.

Subcellular locationi

GO - Cellular componenti

Keywords - Cellular componenti

Secreted

Pathology & Biotechi

Organism-specific databases

PharmGKBiPA134916491.

Polymorphism and mutation databases

BioMutaiC10orf25.

PTM / Processingi

Molecule processing

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Signal peptidei1 – 28Sequence analysisAdd BLAST28
ChainiPRO_000001954829 – 122Uncharacterized protein C10orf25Add BLAST94

Amino acid modifications

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Glycosylationi49N-linked (GlcNAc...) asparagineSequence analysis1

Keywords - PTMi

Glycoprotein

Proteomic databases

PaxDbiQ5T742.
PRIDEiQ5T742.

PTM databases

iPTMnetiQ5T742.
PhosphoSitePlusiQ5T742.

Interactioni

Protein-protein interaction databases

STRINGi9606.ENSP00000298298.

Structurei

3D structure databases

ProteinModelPortaliQ5T742.
ModBaseiSearch...
MobiDBiSearch...

Family & Domainsi

Keywords - Domaini

Signal

Phylogenomic databases

eggNOGiENOG410JI6E. Eukaryota.
ENOG41115CR. LUCA.
HOGENOMiHOG000169670.
InParanoidiQ5T742.
PhylomeDBiQ5T742.
TreeFamiTF340712.

Sequencei

Sequence statusi: Complete.

Sequence processingi: The displayed sequence is further processed into a mature form.

Q5T742-1 [UniParc]FASTAAdd to basket

« Hide

        10         20         30         40         50
MVPGPPESVV RFFLWFCFLL PPTRKASCDP RDLKSCNRPC VWSRLLKPNS
60 70 80 90 100
SLSNLETAYF PQILRFLRPW YFSRSHLNYH QKAPARWEWL YSIYRKGTKA
110 120
QRRNVLRSPC APPQPSWPCS VI
Length:122
Mass (Da):14,441
Last modified:May 18, 2010 - v3
Checksum:iECA0C0FF5E008861
GO

Natural variant

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Natural variantiVAR_06160361P → L. Corresponds to variant dbSNP:rs41301609Ensembl.1
Natural variantiVAR_04710263I → N3 PublicationsCorresponds to variant dbSNP:rs12269028Ensembl.1

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AK055129 mRNA. Translation: BAB70858.1.
AL353801 Genomic DNA. Translation: CAI13067.1.
CH471160 Genomic DNA. Translation: EAW86630.1.
BC130369 mRNA. Translation: AAI30370.1.
BC130395 mRNA. Translation: AAI30396.1.
RefSeqiNP_001034469.2. NM_001039380.3.
XP_016871384.1. XM_017015895.1.
UniGeneiHs.707791.

Genome annotation databases

GeneIDi220979.
KEGGihsa:220979.

Keywords - Coding sequence diversityi

Polymorphism

Similar proteinsi

Entry informationi

Entry nameiCJ025_HUMAN
AccessioniPrimary (citable) accession number: Q5T742
Secondary accession number(s): A1L424, Q96NM5
Entry historyiIntegrated into UniProtKB/Swiss-Prot: July 19, 2005
Last sequence update: May 18, 2010
Last modified: August 30, 2017
This is version 87 of the entry and version 3 of the sequence. See complete history.
Entry statusiReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
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.

Miscellaneousi

Keywords - Technical termi

Complete proteome, Reference proteome

Documents

  1. Human chromosome 10
    Human chromosome 10: entries, gene names and cross-references to MIM
  2. Human entries with polymorphisms or disease mutations
    List of human entries with polymorphisms or disease mutations
  3. Human polymorphisms and disease mutations
    Index of human polymorphisms and disease mutations