Q86SH4 (PRNT_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 50.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Putative testis-specific prion protein Alternative name(s): Protein M8 | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) [Reference proteome] | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 94 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Uncertain |
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 component | Secreted |
| Coding sequence diversity | Polymorphism |
| Domain | Signal |
| PTM | Glycoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular_component | extracellular region Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 18 | 18 | Potential | ||||||
| Chain | 19 – 94 | 76 | Putative testis-specific prion protein | PRO_0000320163 | |||||
Amino acid modifications | |||||||||
| Glycosylation | 44 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 50 | 1 | T → S. Corresponds to variant rs7270737 [ dbSNP | Ensembl ]. | VAR_039151 | |||||
Sequences
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. |
| IPI | IPI00218954. |
| UniGene | Hs.126516. |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000404306. |
Proteomic databases | |
| PRIDE | Q86SH4. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000326539; ENSP00000321242; ENSG00000180259. ENST00000418528; ENSP00000409280; ENSG00000180259. ENST00000423718; ENSP00000404306; ENSG00000180259. |
Organism-specific databases | |
| GeneCards | GC20M004660. |
| HGNC | HGNC:18046. PRNT. |
| HPA | HPA045000. |
| neXtProt | NX_Q86SH4. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOGENOM | HOG000232079. |
| HOVERGEN | HBG067398. |
| InParanoid | Q86SH4. |
| OrthoDB | EOG48SGW6. |
| PhylomeDB | Q86SH4. |
Gene expression databases | |
| Bgee | Q86SH4. |
| CleanEx | HS_PRNT. |
| Genevestigator | Q86SH4. |
Family and domain databases | |
| ProtoNet | Search... |
Entry information
| Entry name | PRNT_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q86SH4 Secondary accession number(s): B2RPD9, B7ZBI9 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| 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. | ||||||||
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 |

Clusters with
