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Q86SH4 (PRNT_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 3, 2013. Version 50. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (3) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Putative testis-specific prion protein
Alternative name(s):
Protein M8
Gene names
Name:PRNT
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length94 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceUncertain

General annotation (Comments)

Subcellular location

Secreted Potential.

Tissue specificity

Specifically expressed in adult testis. Ref.1

Miscellaneous

This putative protein is only present in primates and not in other mammals.

Caution

Could be the product of a pseudogene. According to Ref.5, no evidence has been tendered concerning the existence of this protein.

According to Ref.1, it is related to the prion family because it is found in the same genomic cluster as PRNP and PRND. However, it does not share any sequence similarity with these 2 proteins.

Ontologies

Keywords
   Cellular componentSecreted
   Coding sequence diversityPolymorphism
   DomainSignal
   PTMGlycoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular_componentextracellular region

Inferred from electronic annotation. Source: UniProtKB-SubCell

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 1818 Potential
Chain19 – 9476Putative testis-specific prion protein
PRO_0000320163

Amino acid modifications

Glycosylation441N-linked (GlcNAc...) Potential

Natural variations

Natural variant501T → S.
Corresponds to variant rs7270737 [ dbSNP | Ensembl ].
VAR_039151

Sequences

Sequence LengthMass (Da)Tools
Q86SH4 [UniParc].

Last modified June 1, 2003. Version 1.
Checksum: 7A6726D67325D115

FASTA9410,756
        10         20         30         40         50         60 
MQHSLVFFFA VILHLSHLLH LDASIHPFRL PFSSKPFLLI PMSNTTLPHT AWPLSFLHQT 

        70         80         90 
VSTLKAVAVT HSLWHLQIPV DCQACNRKSK KIYC 

« Hide

References

« Hide 'large scale' references
[1]"Genomic characterization of the human prion protein (PrP) gene locus."
Makrinou E., Collinge J., Antoniou M.
Mamm. Genome 13:696-703(2002) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY.
Tissue: Testis.
[2]"The DNA sequence and comparative analysis of human chromosome 20."
Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L., Bailey J., Barlow K.F., Bates K.N., Beard L.M., Beare D.M., Beasley O.P., Bird C.P., Blakey S.E. expand/collapse author list , Bridgeman A.M., Brown A.J., Buck D., Burrill W.D., Butler A.P., Carder C., Carter N.P., Chapman J.C., Clamp M., Clark G., Clark L.N., Clark S.Y., Clee C.M., Clegg S., Cobley V.E., Collier R.E., Connor R.E., Corby N.R., Coulson A., Coville G.J., Deadman R., Dhami P.D., Dunn M., Ellington A.G., Frankland J.A., Fraser A., French L., Garner P., Grafham D.V., Griffiths C., Griffiths M.N.D., Gwilliam R., Hall R.E., Hammond S., Harley J.L., Heath P.D., Ho S., Holden J.L., Howden P.J., Huckle E., Hunt A.R., Hunt S.E., Jekosch K., Johnson C.M., Johnson D., Kay M.P., Kimberley A.M., King A., Knights A., Laird G.K., Lawlor S., Lehvaeslaiho M.H., Leversha M.A., Lloyd C., Lloyd D.M., Lovell J.D., Marsh V.L., Martin S.L., McConnachie L.J., McLay K., McMurray A.A., Milne S.A., Mistry D., Moore M.J.F., Mullikin J.C., Nickerson T., Oliver K., Parker A., Patel R., Pearce T.A.V., Peck A.I., Phillimore B.J.C.T., Prathalingam S.R., Plumb R.W., Ramsay H., Rice C.M., Ross M.T., Scott C.E., Sehra H.K., Shownkeen R., Sims S., Skuce C.D., Smith M.L., Soderlund C., Steward C.A., Sulston J.E., Swann R.M., Sycamore N., Taylor R., Tee L., Thomas D.W., Thorpe A., Tracey A., Tromans A.C., Vaudin M., Wall M., Wallis J.M., Whitehead S.L., Whittaker P., Willey D.L., Williams L., Williams S.A., Wilming L., Wray P.W., Hubbard T., Durbin R.M., Bentley D.R., Beck S., Rogers J.
Nature 414:865-871(2001) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. expand/collapse author list , Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H., Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K., Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D., Hunkapiller M.W., Myers E.W., Venter J.C.
Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[4]"Comparative genomic organization of the human and bovine PRNP locus."
Choi S.-H., Kim I.-C., Kim D.-S., Kim D.-W., Chae S.-H., Choi H.-H., Choi I., Yeo J.-S., Song M.-N., Park H.-S.
Genomics 87:598-607(2006) [PubMed] [Europe PMC] [Abstract]
Cited for: PHYLOGENY.
[5]"The prion protein family: diversity, rivalry, and dysfunction."
Watts J.C., Westaway D.
Biochim. Biophys. Acta 1772:654-672(2007) [PubMed] [Europe PMC] [Abstract]
Cited for: PHYLOGENY.
[6]"Comparative genomic analysis of prion genes."
Premzl M., Gamulin V.
BMC Genomics 8:1-1(2007) [PubMed] [Europe PMC] [Abstract]
Cited for: PHYLOGENY.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AJ427539 mRNA. Translation: CAD20690.1.
AJ427540 mRNA. Translation: CAD20691.1.
AL133396 Genomic DNA. Translation: CAX15126.1.
CH471133 Genomic DNA. Translation: EAX10447.1.
IPIIPI00218954.
UniGeneHs.126516.

3D structure databases

ModBaseSearch...

Protein-protein interaction databases

STRING9606.ENSP00000404306.

Proteomic databases

PRIDEQ86SH4.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000326539; ENSP00000321242; ENSG00000180259.
ENST00000418528; ENSP00000409280; ENSG00000180259.
ENST00000423718; ENSP00000404306; ENSG00000180259.

Organism-specific databases

GeneCardsGC20M004660.
HGNCHGNC:18046. PRNT.
HPAHPA045000.
neXtProtNX_Q86SH4.
GenAtlasSearch...

Phylogenomic databases

HOGENOMHOG000232079.
HOVERGENHBG067398.
InParanoidQ86SH4.
OrthoDBEOG48SGW6.
PhylomeDBQ86SH4.

Gene expression databases

BgeeQ86SH4.
CleanExHS_PRNT.
GenevestigatorQ86SH4.

Family and domain databases

ProtoNetSearch...

Entry information

Entry namePRNT_HUMAN
AccessionPrimary (citable) accession number: Q86SH4
Secondary accession number(s): B2RPD9, B7ZBI9
Entry history
Integrated into UniProtKB/Swiss-Prot: February 26, 2008
Last sequence update: June 1, 2003
Last modified: April 3, 2013
This is version 50 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (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.

Relevant documents

Human chromosome 20

Human chromosome 20: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations