Details for: MNS1

Gene ID: 55329

Symbol: MNS1

Ensembl ID: ENSG00000138587

Description: meiosis specific nuclear structural 1

Associated with

Other Information

Genular Protein ID: 2604095093

Symbol: MNS1_HUMAN

Name: N/A

UniProtKB Accession Codes:

Q8NEH6 Q8IYT6 Q9NUP4

Database IDs:

AGR 1 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID 1 BioGRID-ORCS 1 BioMuta 1 CCDS 1 CTD 1 ChiTaRS 1 DMDM 1 DNASU 1 DisGeNET 1 EMBL 3 EMDB 2 EPD 1 Ensembl 1 GO 12 GeneCards 1 GeneTree 1 Genevisible 1 GenomeRNAi 1 HGNC 2 HOGENOM 1 HPA 1 InParanoid 1 IntAct 1 InterPro 2 KEGG 1 MANE-Select 1 MIM 3 MINT 1 MalaCards 1 MassIVE 1 NCBI Taxonomy 1 OMA 1 OpenTargets 1 OrthoDB 1 PANTHER 2 PDB 3 PDBsum 2 PRO 1 PathwayCommons 1 PaxDb 1 PeptideAtlas 1 Pfam 1 PharmGKB 1 Pharos 1 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 1 Pumba 1 RNAct 1 RefSeq 1 SMR 1 STRING 1 SignaLink 1 TreeFam 1 UCSC 1 UniProtKB 2 VEuPathDB 1 eggNOG 1 iPTMnet 1 jPOST 1 neXtProt 1

Citations:

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 36191189

Title: SPACA9 is a lumenal protein of human ciliary singlet and doublet microtubules.

PubMed ID: 36191189

DOI: 10.1073/pnas.2207605119

PubMed ID: 30148830

Title: Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.

PubMed ID: 30148830

DOI: 10.1371/journal.pgen.1007602

PubMed ID: 31534215

Title: MNS1 variant associated with situs inversus and male infertility.

PubMed ID: 31534215

DOI: 10.1038/s41431-019-0489-z

Sequence Information:

  • Length: 495
  • Mass: 60571
  • Checksum: 85EF33C9A659FBD1
  • Sequence:
    • MGSKRRNLSC SERHQKLVDE NYCKKLHVQA LKNVNSQIRN QMVQNENDNR VQRKQFLRLL 
QNEQFELDME EAIQKAEENK RLKELQLKQE EKLAMELAKL KHESLKDEKM RQQVRENSIE 
LRELEKKLKA AYMNKERAAQ IAEKDAIKYE QMKRDAEIAK TMMEEHKRII KEENAAEDKR 
NKAKAQYYLD LEKQLEEQEK KKQEAYEQLL KEKLMIDEIV RKIYEEDQLE KQQKLEKMNA 
MRRYIEEFQK EQALWRKKKR EEMEEENRKI IEFANMQQQR EEDRMAKVQE NEEKRLQLQN 
ALTQKLEEML RQREDLEQVR QELYQEEQAE IYKSKLKEEA EKKLRKQKEM KQDFEEQMAL 
KELVLQAAKE EEENFRKTML AKFAEDDRIE LMNAQKQRMK QLEHRRAVEK LIEERRQQFL 
ADKQRELEEW QLQQRRQGFI NAIIEEERLK LLKEHATNLL GYLPKGVFKK EDDIDLLGEE 
FRKVYQQRSE ICEEK

Genular Protein ID: 1354038393

Symbol: B3KQ70_HUMAN

Name: N/A

UniProtKB Accession Codes:

B3KQ70

Database IDs:

ARBA 11 AlphaFoldDB 1 BioGRID-ORCS 1 CTD 1 ChiTaRS 1 DNASU 1 EMBL 4 GO 2 GenomeRNAi 1 InterPro 2 KEGG 1 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PeptideAtlas 1 Pfam 2 PharmGKB 1 RefSeq 1 SAM 1

Citations:

PubMed ID: 11181995

Title: The sequence of the human genome.

PubMed ID: 11181995

DOI: 10.1126/science.1058040

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

Sequence Information:

  • Length: 363
  • Mass: 44641
  • Checksum: 80D75C7EB562F8B3
  • Sequence:
    • MNKERAAQIA EKDAIKYEQM KRDAEIAKTM MEEHKRIIKE ENAAEDKRNK AKAQYYLDLE 
KQLEEQEKKK QEAYEQLLKE KLMIDEIVRK IYEEDQLEKQ QKLEKMNAMR RYIEEFQKEQ 
ALWRKKKREE MEEENRKIIE FANMQQQREE DRMAKVQENE EKRLQLQNAL TQKLEEMLRQ 
REDLEQVRQE LYQEEQAEIY KSKLKEEAEK KLRKQKEMKQ DFEEQMALKE LVLQAAKEEE 
ENFRKTMLAK FAEDDRIELM NAQKQRMKQL EHRRAVEKLI EERRQQFLAD KQRELEEWQL 
QQRRQGFINA IIEEERLKLL KEHATNLLGY LPKGVFKKED DIDLLGEEFR KVYQQRSEIC 
EEK

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.