Type | Description |
---|---|
Definition | nuclear pore associated protein 1 |
Date | Results | Publications |
---|---|---|
2015-01-10 13:31:00 | NPAP1 is specific to primate species and absent from the 15q11q13-orthologous regions in all nonprimate mammals. | 24482533 |
2013-01-26 10:21:00 | C15orf2 is part of the nuclear pore complex or its associated molecular networks. | 22694955 |
2010-10-20 13:20:00 | C15orf2 gene is imprinted, with monoallelic expression from the paternal allele in fetal brain. | 17337158 |
2010-07-19 11:23:00 | These results indicate that C15orf2 might have an important role in human biology and that a deficiency of C15orf2 might contribute to Prader-Willi syndrome. | 20020165 |
2010-02-15 11:16:00 | The results from this study show an involvement of microdeletions at 15q11.2 that predispose patients to idiopathic generalized epilepsies. | 19843651 |
Type | IDs |
---|---|
Synonymous | C15orf2 |
Gene |
UniProtKB-ID:
NPAP1_HUMAN
UniprotKB:
Q9NZP6
UniParc:
UPI00001AFA1B
EMBL:
AC100720,
AF179681
Ensembl:
ENSG00000185823
KO:
hsa:23742
|
Nucleutide sequences |
EMBL-CDS:
AAF72107.1
Ensembl_TRS:
ENST00000329468
|
Protein sequencees |
Ensembl_PRO:
ENSP00000333735
RefSeq:
NP_061831.2
|
Others |
UniRef100:
UniRef100_Q9NZP6
UniRef90:
UniRef90_Q9NZP6
UniRef50:
UniRef50_Q9NZP6
UniGene:
Hs.649663
CCDS:
CCDS10015.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
{{protein.nucleotideVersion}}
Ensembl: {{protein.nucleotideEnsembl}} |
{{protein.proteinVersion}}
Ensembl: {{protein.proteinEnsembl}} |
{{uniprot}} , |
Definition: {{{protein.definition}}}Transcript Veriant:{{protein.transcriptVeriant}} Status: {{protein.status}} |
||||
Location | {{protein.contigId}} ( {{protein.positionStart}}..{{protein.positionEnd}} , {{protein.orientation}} ) | |||||||
Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
{{conservedDomain.comments == '' || conservedDomain.comments == null ? "-" : conservedDomain.comments }} |
Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
{{conservedDomain.comments == '' || conservedDomain.comments == null ? "-" : conservedDomain.comments }} |
暂无数据
Pubmed编号 | 文献信息 | 发表日期 | 相关基因 |
---|---|---|---|
32694731 |
Nat Metab Michael Aregger , Keith A Lawson , Maximillian Billmann , Michael Costanzo , Amy H Y Tong , Katherine Chan , Mahfuzur Rahman , Kevin R Brown , Catherine Ross , Matej Usaj , Lucy Nedyalkova , Olga Sizova , Andrea Habsid , Judy Pawling , Zhen-Yuan Lin , Hala Abdouni , Cassandra J Wong , Alexander Weiss , Patricia Mero , James W Dennis , Anne-Claude Gingras , Chad L Myers , Brenda J Andrews , Charles Boone , Jason Moffat |
2020-06-01 | - |
24482533 |
Genome Biol Evol Lisa C Neumann , Nathalie Feiner , Axel Meyer , Karin Buiting , Bernhard Horsthemke |
2014-02-01 | - |
24024966 |
Genome-wide association study of chronic periodontitis in a general German population. J. Clin. Periodontol. Alexander Teumer , Birte Holtfreter , Uwe Völker , Astrid Petersmann , Matthias Nauck , Reiner Biffar , Henry Völzke , Heyo K Kroemer , Peter Meisel , Georg Homuth , Thomas Kocher |
2013-11-01 |
PDCD6IP,
ST20-MTHFS,
CDH13,
LOC101927025,
LOC101927661,
LOC101928114,
LOC101928134,
LOC102724761,
MTHFS,
CHD1,
PTPRT,
GPN1,
C1orf87,
WDR36,
NRSN1,
PSMA8,
ZNF524,
CCDC13,
NKAIN2,
FAM47A,
ZNF579,
PARP15,
DEFA1,
C10orf91,
ADAMTS15,
ABCA1,
EPHA3,
ETS2,
NLGN1,
DKK1,
KDM4B,
NPAP1,
FRG1,
ERC2,
DAOA,
LINC00907,
SUMF1,
NKAIN3,
GRIK1,
LRP12,
HLA-DOA,
FOXA1,
BIRC5,
C12orf74,
HMX3,
IGF2R,
IGL,
KCNJ16,
FAM180A,
LBP,
ST20,
LOC400867,
NPM1P2,
FAM135B,
PIK3C3,
LRP1B,
ETAA1,
RBFOX1,
PGPEP1,
ETNK2,
NMUR2,
RGMA,
ERGIC1,
PTEN,
SEMA6A,
RIT2,
ROBO2,
RYR3,
BCORL1,
SCN2A,
BLK,
SETMAR,
CSMD1,
MFSD1,
SMURF2,
PRB2,
SNRPN,
SNTB1,
SS18,
TGIF1,
TIMP2,
ROCK1P1,
VPREB1,
ZNF385D,
THSD4,
CAMK4,
LINC00208,
RAB6C,
FAM126A,
FIZ1,
WDR73,
ITGA8,
ACTN1,
ACTN2,
MBD2,
HS6ST2,
IQSEC1
|
23376485 |
Proteomic analysis of podocyte exosome-enriched fraction from normal human urine. J Proteomics Marco Prunotto , Annarita Farina , Lydie Lane , Agnès Pernin , Jürg Schifferli , Denis F Hochstrasser , Pierre Lescuyer , Solange Moll |
2013-04-26 |
CDH2,
GNPDA1,
C1orf68,
PDCD6IP,
PDCD6,
TOM1L1,
CDH6,
IL18BP,
DPP3,
SNUPN,
ARPC5,
CDH11,
ARPC4,
ARPC3,
ARPC1B,
ACTR3,
ACTR2,
TSPAN1,
ARPC2,
ACTR1B,
ACTR1A,
CDH13,
PDIA6,
TRAP1,
PDZK1IP1,
ATP6AP2,
DHRS2,
NUTF2,
FLOT1,
PSMD14,
RIDA,
GLYAT,
ZMPSTE24,
STUB1,
RTN3,
LANCL1,
CRISP3,
SIRPB1,
AKR1A1,
TFG,
TUBA1B,
BPNT1,
TUBB4B,
BTN2A2,
NDRG1,
RACK1,
ST3GAL6,
CPQ,
WFDC2,
BASP1,
IFITM3,
CDSN,
LYPLA1,
FAM3C,
ACAA2,
VAV3,
TOMM40,
BAIAP2,
ATP5H,
CEACAM5,
CAP1,
VAT1,
FBLN5,
CIB1,
GLRX3,
PROCR,
ARL6IP5,
ARPC1A,
OLFM4,
CEL,
CCT7,
CCT4,
CCT2,
NPC2,
DNPH1,
PAICS,
MYL12A,
ATP5L,
YKT6,
PMVK,
GNA13,
B3GNT2,
CCT8,
CETP,
CFL1,
PTGES3,
RBBP9,
MASP2,
CTSC,
GIPC1,
AHCYL1,
IQGAP2,
VAMP5,
CFTR,
ALDH1L1,
FTCD,
RUVBL2,
PGRMC1,
FGL2
|
22694955 |
Hum. Mol. Genet. Lisa C Neumann , Yolanda Markaki , Emil Mladenov , Daniel Hoffmann , Karin Buiting , Bernhard Horsthemke |
2012-09-15 |
NPAP1
|
21873635 |
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Brief. Bioinformatics Pascale Gaudet , Michael S Livstone , Suzanna E Lewis , Paul D Thomas |
2011-09-01 | - |
20020165 |
Neurogenetics Michaela Wawrzik , Unga Arifa Unmehopa , Dick Frans Swaab , Johannes van de Nes , Karin Buiting , Bernhard Horsthemke |
2010-05-01 |
NPAP1
|
19843651 |
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies. Brain Carolien G F de Kovel , Holger Trucks , Ingo Helbig , Heather C Mefford , Carl Baker , Costin Leu , Christian Kluck , Hiltrud Muhle , Sarah von Spiczak , Philipp Ostertag , Tanja Obermeier , Ailing A Kleefuss-Lie , Kerstin Hallmann , Michael Steffens , Verena Gaus , Karl M Klein , Hajo M Hamer , Felix Rosenow , Eva H Brilstra , Dorothée Kasteleijn-Nolst Trenité , Marielle E M Swinkels , Yvonne G Weber , Iris Unterberger , Fritz Zimprich , Lydia Urak , Martha Feucht , Karoline Fuchs , Rikke S Møller , Helle Hjalgrim , Peter De Jonghe , Arvid Suls , Ina-Maria Rückert , Heinz-Erich Wichmann , Andre Franke , Stefan Schreiber , Peter Nürnberg , Christian E Elger , Holger Lerche , Ulrich Stephani , Bobby P C Koeleman , Dick Lindhout , Evan E Eichler , Thomas Sander |
2010-01-01 |
FOPNL,
NPAP1
|
19066619 |
A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome. Eur J Hum Genet Deniz Kanber , Jacques Giltay , Dagmar Wieczorek , Corinna Zogel , Ron Hochstenbach , Almuth Caliebe , Alma Kuechler , Bernhard Horsthemke , Karin Buiting |
2009-05-01 | - |
18976975 |
Genome-scale RNAi screen for host factors required for HIV replication. Cell Host Microbe Honglin Zhou , Min Xu , Qian Huang , Adam T Gates , Xiaohua D Zhang , John C Castle , Erica Stec , Marc Ferrer , Berta Strulovici , Daria J Hazuda , Amy S Espeseth |
2008-11-13 | - |
排名 | 科研单位 | 文献 |
---|---|---|
{{affIndex+1}} |
{{aff.value}} |
{{aff.size}} |
目前还没有研究热点单位
排名 | 研究人员 | 文献 |
---|---|---|
{{authorIndex+1}} |
{{author.value}} |
{{author.size}} |
目前还没有研究热点人员