Q8NEH6 (MNS1_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 69.
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: Meiosis-specific nuclear structural protein 1 | ||
| 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 | 495 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | May play a role in the control of meiotic division and germ cell differentiation through regulation of pairing and recombination during meiosis By similarity. |
| Subcellular location | Nucleus By similarity. |
| Sequence similarities | Belongs to the MNS1 family. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Meiosis |
| Cellular component | Nucleus |
| Coding sequence diversity | Polymorphism |
| Domain | Coiled coil |
| PTM | Phosphoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | meiosis Inferred from electronic annotation. Source: UniProtKB-KW |
| Cellular_component | intermediate filament Inferred from electronic annotation. Source: Compara nuclear envelopeInferred from electronic annotation. Source: Compara |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 495 | 495 | Meiosis-specific nuclear structural protein 1 | PRO_0000298921 | |||||
Regions | |||||||||
| Coiled coil | 28 – 410 | 383 | Potential | ||||||
| Compositional bias | 63 – 373 | 311 | Glu-rich | ||||||
Amino acid modifications | |||||||||
| Modified residue | 244 | 1 | Phosphotyrosine By similarity | ||||||
Natural variations | |||||||||
| Natural variant | 10 | 1 | C → Y. Corresponds to variant rs34807682 [ dbSNP | Ensembl ]. | VAR_034737 | |||||
| Natural variant | 55 | 1 | Q → P. Corresponds to variant rs1715919 [ dbSNP | Ensembl ]. | VAR_034738 | |||||
| Natural variant | 216 | 1 | I → T. Corresponds to variant rs35775595 [ dbSNP | Ensembl ]. | VAR_034739 | |||||
| Natural variant | 244 | 1 | Y → H. Ref.2 Corresponds to variant rs17852882 [ dbSNP | Ensembl ]. | VAR_034740 | |||||
| Natural variant | 426 | 1 | E → G. Ref.2 Corresponds to variant rs17853357 [ dbSNP | Ensembl ]. | VAR_034741 | |||||
Sequences
| ||||||||||||||||||
References
| [1] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: Placenta. |
| [2] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANTS HIS-244 AND GLY-426. Tissue: Testis. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK002084 mRNA. Translation: BAA92077.1. BC031046 mRNA. Translation: AAH31046.1. BC034991 mRNA. Translation: AAH34991.1. |
| IPI | IPI00549955. |
| RefSeq | NP_060835.1. NM_018365.2. |
| UniGene | Hs.444483. |
3D structure databases | |
| ProteinModelPortal | Q8NEH6. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q8NEH6. 1 interaction. |
| MINT | MINT-1459670. |
| STRING | 9606.ENSP00000260453. |
PTM databases | |
| PhosphoSite | Q8NEH6. |
Polymorphism databases | |
| DMDM | 156632590. |
Proteomic databases | |
| PaxDb | Q8NEH6. |
| PRIDE | Q8NEH6. |
Protocols and materials databases | |
| DNASU | 55329. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000260453; ENSP00000260453; ENSG00000138587. |
| GeneID | 55329. |
| KEGG | hsa:55329. |
| UCSC | uc002adr.2. human. |
Organism-specific databases | |
| CTD | 55329. |
| GeneCards | GC15M056720. |
| HGNC | HGNC:29636. MNS1. |
| HPA | HPA039975. HPA040382. |
| MIM | 610766. gene. |
| neXtProt | NX_Q8NEH6. |
| PharmGKB | PA142671346. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG116635. |
| HOGENOM | HOG000006500. |
| HOVERGEN | HBG108140. |
| InParanoid | Q8NEH6. |
| OMA | AKTMMEE. |
| OrthoDB | EOG4QNMWG. |
| PhylomeDB | Q8NEH6. |
Gene expression databases | |
| ArrayExpress | Q8NEH6. |
| Bgee | Q8NEH6. |
| CleanEx | HS_MNS1. |
| Genevestigator | Q8NEH6. |
Family and domain databases | |
| InterPro | IPR026504. MNS1. [Graphical view] |
| PANTHER | PTHR19265. PTHR19265. 1 hit. |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 55329. |
| NextBio | 59614. |
| SOURCE | Search... |
Entry information
| Entry name | MNS1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8NEH6 Secondary accession number(s): Q8IYT6, Q9NUP4 | ||||||||
| Entry history |
| ||||||||
| 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 15 Human chromosome 15: 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 |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

Clusters with
