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Q8NEH6 (MNS1_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 3, 2013. Version 69. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | 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:
Meiosis-specific nuclear structural protein 1
Gene names
Name:MNS1
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length495 AA.
Sequence statusComplete.
Protein existenceEvidence 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 processMeiosis
   Cellular componentNucleus
   Coding sequence diversityPolymorphism
   DomainCoiled coil
   PTMPhosphoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological_processmeiosis

Inferred from electronic annotation. Source: UniProtKB-KW

   Cellular_componentintermediate filament

Inferred from electronic annotation. Source: Compara

nuclear envelope

Inferred from electronic annotation. Source: Compara

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 495495Meiosis-specific nuclear structural protein 1
PRO_0000298921

Regions

Coiled coil28 – 410383 Potential
Compositional bias63 – 373311Glu-rich

Amino acid modifications

Modified residue2441Phosphotyrosine By similarity

Natural variations

Natural variant101C → Y.
Corresponds to variant rs34807682 [ dbSNP | Ensembl ].
VAR_034737
Natural variant551Q → P.
Corresponds to variant rs1715919 [ dbSNP | Ensembl ].
VAR_034738
Natural variant2161I → T.
Corresponds to variant rs35775595 [ dbSNP | Ensembl ].
VAR_034739
Natural variant2441Y → H. Ref.2
Corresponds to variant rs17852882 [ dbSNP | Ensembl ].
VAR_034740
Natural variant4261E → G. Ref.2
Corresponds to variant rs17853357 [ dbSNP | Ensembl ].
VAR_034741

Sequences

Sequence LengthMass (Da)Tools
Q8NEH6 [UniParc].

Last modified August 21, 2007. Version 2.
Checksum: 85EF33C9A659FBD1

FASTA49560,571
        10         20         30         40         50         60 
MGSKRRNLSC SERHQKLVDE NYCKKLHVQA LKNVNSQIRN QMVQNENDNR VQRKQFLRLL 

        70         80         90        100        110        120 
QNEQFELDME EAIQKAEENK RLKELQLKQE EKLAMELAKL KHESLKDEKM RQQVRENSIE 

       130        140        150        160        170        180 
LRELEKKLKA AYMNKERAAQ IAEKDAIKYE QMKRDAEIAK TMMEEHKRII KEENAAEDKR 

       190        200        210        220        230        240 
NKAKAQYYLD LEKQLEEQEK KKQEAYEQLL KEKLMIDEIV RKIYEEDQLE KQQKLEKMNA 

       250        260        270        280        290        300 
MRRYIEEFQK EQALWRKKKR EEMEEENRKI IEFANMQQQR EEDRMAKVQE NEEKRLQLQN 

       310        320        330        340        350        360 
ALTQKLEEML RQREDLEQVR QELYQEEQAE IYKSKLKEEA EKKLRKQKEM KQDFEEQMAL 

       370        380        390        400        410        420 
KELVLQAAKE EEENFRKTML AKFAEDDRIE LMNAQKQRMK QLEHRRAVEK LIEERRQQFL 

       430        440        450        460        470        480 
ADKQRELEEW QLQQRRQGFI NAIIEEERLK LLKEHATNLL GYLPKGVFKK EDDIDLLGEE 

       490 
FRKVYQQRSE ICEEK 

« Hide

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. expand/collapse author list , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., 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.
IPIIPI00549955.
RefSeqNP_060835.1. NM_018365.2.
UniGeneHs.444483.

3D structure databases

ProteinModelPortalQ8NEH6.
ModBaseSearch...

Protein-protein interaction databases

IntActQ8NEH6. 1 interaction.
MINTMINT-1459670.
STRING9606.ENSP00000260453.

PTM databases

PhosphoSiteQ8NEH6.

Polymorphism databases

DMDM156632590.

Proteomic databases

PaxDbQ8NEH6.
PRIDEQ8NEH6.

Protocols and materials databases

DNASU55329.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000260453; ENSP00000260453; ENSG00000138587.
GeneID55329.
KEGGhsa:55329.
UCSCuc002adr.2. human.

Organism-specific databases

CTD55329.
GeneCardsGC15M056720.
HGNCHGNC:29636. MNS1.
HPAHPA039975.
HPA040382.
MIM610766. gene.
neXtProtNX_Q8NEH6.
PharmGKBPA142671346.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG116635.
HOGENOMHOG000006500.
HOVERGENHBG108140.
InParanoidQ8NEH6.
OMAAKTMMEE.
OrthoDBEOG4QNMWG.
PhylomeDBQ8NEH6.

Gene expression databases

ArrayExpressQ8NEH6.
BgeeQ8NEH6.
CleanExHS_MNS1.
GenevestigatorQ8NEH6.

Family and domain databases

InterProIPR026504. MNS1.
[Graphical view]
PANTHERPTHR19265. PTHR19265. 1 hit.
ProtoNetSearch...

Other

GenomeRNAi55329.
NextBio59614.
SOURCESearch...

Entry information

Entry nameMNS1_HUMAN
AccessionPrimary (citable) accession number: Q8NEH6
Secondary accession number(s): Q8IYT6, Q9NUP4
Entry history
Integrated into UniProtKB/Swiss-Prot: August 21, 2007
Last sequence update: August 21, 2007
Last modified: April 3, 2013
This is version 69 of the entry and version 2 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 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