NEK9 (NIMA related kinase 9) - Rat Genome Database

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Gene: NEK9 (NIMA related kinase 9) Homo sapiens
Analyze
Symbol: NEK9
Name: NIMA related kinase 9
RGD ID: 1316228
HGNC Page HGNC
Description: Enables protein kinase binding activity. Predicted to be involved in cell division and protein phosphorylation. Colocalizes with centrosome. Implicated in lethal congenital contracture syndrome.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: APUG; DKFZp434D0935; LCCS10; MGC138306; MGC16714; NC; Nek8; NERCC; NERCC1; nercc1 kinase; never in mitosis A-related kinase 9; NIMA (never in mitosis gene a)- related kinase 9; nimA-related kinase 8; NIMA-related kinase 9; NIMA-related kinase Nek8; nimA-related protein kinase 9; serine/threonine-protein kinase Nek9
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1475,079,353 - 75,127,344 (-)EnsemblGRCh38hg38GRCh38
GRCh381475,079,353 - 75,127,637 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371475,546,056 - 75,593,751 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361474,620,728 - 74,663,389 (-)NCBINCBI36hg18NCBI36
Build 341474,620,727 - 74,663,389NCBI
Celera1455,586,461 - 55,631,402 (-)NCBI
Cytogenetic Map14q24.3NCBI
HuRef1455,716,982 - 55,761,929 (-)NCBIHuRef
CHM1_11475,486,591 - 75,531,543 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
centrosome  (IDA)
cytosol  (TAS)
nucleus  (IEA)

Molecular Function

References

Additional References at PubMed
PMID:8889548   PMID:11864968   PMID:12056414   PMID:12101123   PMID:12477932   PMID:12508121   PMID:12840024   PMID:14660563   PMID:15019993   PMID:15489334   PMID:16902406   PMID:17081983  
PMID:17192257   PMID:17314511   PMID:17353931   PMID:17443675   PMID:18029348   PMID:18976975   PMID:19001501   PMID:19941817   PMID:20360068   PMID:20508983   PMID:20562859   PMID:20873783  
PMID:21454704   PMID:21642957   PMID:21735226   PMID:22818914   PMID:22863883   PMID:22939624   PMID:23414517   PMID:23482567   PMID:23665325   PMID:24067654   PMID:24147044   PMID:25131192  
PMID:25147182   PMID:25281560   PMID:25852190   PMID:25921289   PMID:26186194   PMID:26496610   PMID:26522158   PMID:26673895   PMID:26676776   PMID:26908619   PMID:26956052   PMID:26972000  
PMID:27153399   PMID:27173435   PMID:27542412   PMID:28380382   PMID:28514442   PMID:28515276   PMID:28611215   PMID:28630147   PMID:29276125   PMID:29467282   PMID:29472518   PMID:29669786  
PMID:30021884   PMID:30166453   PMID:30890647   PMID:30948266   PMID:31091453   PMID:31732153   PMID:31857374   PMID:32098687   PMID:32184261   PMID:32235678   PMID:32353859   PMID:32807901  
PMID:32814769   PMID:33060197   PMID:33845483   PMID:34079125  


Genomics

Comparative Map Data
NEK9
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1475,079,353 - 75,127,344 (-)EnsemblGRCh38hg38GRCh38
GRCh381475,079,353 - 75,127,637 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371475,546,056 - 75,593,751 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361474,620,728 - 74,663,389 (-)NCBINCBI36hg18NCBI36
Build 341474,620,727 - 74,663,389NCBI
Celera1455,586,461 - 55,631,402 (-)NCBI
Cytogenetic Map14q24.3NCBI
HuRef1455,716,982 - 55,761,929 (-)NCBIHuRef
CHM1_11475,486,591 - 75,531,543 (-)NCBICHM1_1
Nek9
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391285,346,288 - 85,386,136 (-)NCBIGRCm39mm39
GRCm39 Ensembl1285,346,288 - 85,386,136 (-)Ensembl
GRCm381285,299,514 - 85,339,362 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1285,299,514 - 85,339,362 (-)EnsemblGRCm38mm10GRCm38
MGSCv371286,640,464 - 86,680,312 (-)NCBIGRCm37mm9NCBIm37
MGSCv361286,188,616 - 86,228,440 (-)NCBImm8
Celera1286,757,015 - 86,796,871 (-)NCBICelera
Cytogenetic Map12D2NCBI
Nek9
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.26104,944,056 - 104,984,538 (-)NCBI
Rnor_6.0 Ensembl6109,124,330 - 109,162,267 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.06109,121,524 - 109,162,433 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.06116,390,523 - 116,435,517 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.46109,345,437 - 109,389,174 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.16109,351,642 - 109,394,468 (-)NCBI
Celera6102,766,488 - 102,807,366 (-)NCBICelera
Cytogenetic Map6q31NCBI
Nek9
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955523446,748 - 482,246 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955523443,832 - 483,397 (+)NCBIChiLan1.0ChiLan1.0
NEK9
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11474,478,387 - 74,522,320 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1474,478,387 - 74,522,320 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01455,633,667 - 55,678,670 (-)NCBIMhudiblu_PPA_v0panPan3
NEK9
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1848,180,203 - 48,218,430 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl848,183,071 - 48,257,646 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha847,864,320 - 47,902,676 (-)NCBI
ROS_Cfam_1.0848,407,827 - 48,446,234 (-)NCBI
UMICH_Zoey_3.1848,078,603 - 48,116,941 (-)NCBI
UNSW_CanFamBas_1.0848,099,872 - 48,138,217 (-)NCBI
UU_Cfam_GSD_1.0848,498,571 - 48,536,910 (-)NCBI
Nek9
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864027,807,701 - 27,847,583 (+)NCBI
SpeTri2.0NW_0049364884,221,099 - 4,261,401 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NEK9
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl798,275,976 - 98,322,469 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1798,275,973 - 98,322,072 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.27104,120,094 - 104,166,188 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NEK9
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12452,297,211 - 52,342,359 (-)NCBI
ChlSab1.1 Ensembl2452,296,261 - 52,342,724 (-)Ensembl
Vero_WHO_p1.0NW_02366605340,527,142 - 40,572,456 (-)NCBI
Nek9
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473426,557,208 - 26,600,777 (+)NCBI

Position Markers
G35839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371475,552,997 - 75,553,099UniSTSGRCh37
Build 361474,622,750 - 74,622,852RGDNCBI36
Celera1455,590,639 - 55,590,741RGD
Cytogenetic Map14q24.3UniSTS
HuRef1455,721,155 - 55,721,257UniSTS
RH93908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371475,559,526 - 75,559,648UniSTSGRCh37
Build 361474,629,279 - 74,629,401RGDNCBI36
Celera1455,597,168 - 55,597,290RGD
Cytogenetic Map14q24.3UniSTS
HuRef1455,727,684 - 55,727,806UniSTS
GeneMap99-GB4 RH Map14199.07UniSTS
D14S1275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371475,570,480 - 75,570,598UniSTSGRCh37
Build 361474,640,233 - 74,640,351RGDNCBI36
Celera1455,608,119 - 55,608,237RGD
Cytogenetic Map14q24.3UniSTS
HuRef1455,738,632 - 55,738,750UniSTS
D14S860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371475,575,827 - 75,575,976UniSTSGRCh37
Build 361474,645,580 - 74,645,729RGDNCBI36
Celera1455,613,449 - 55,613,598RGD
Cytogenetic Map14q24.3UniSTS
HuRef1455,743,977 - 55,744,126UniSTS
Whitehead-RH Map14266.1UniSTS
Whitehead-YAC Contig Map14 UniSTS
NCBI RH Map14837.4UniSTS
STS-AA027231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371475,548,850 - 75,549,064UniSTSGRCh37
Build 361474,618,603 - 74,618,817RGDNCBI36
Celera1455,586,493 - 55,586,707RGD
Cytogenetic Map14q24.3UniSTS
HuRef1455,717,014 - 55,717,228UniSTS
GeneMap99-GB4 RH Map14198.97UniSTS
GDB:335751  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map10q24.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map3q22.2UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map6p21.1-p12.2UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map13q12.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map9q22.32UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
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Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2383
Count of miRNA genes:1080
Interacting mature miRNAs:1304
Transcripts:ENST00000238616, ENST00000553823, ENST00000553945, ENST00000554258, ENST00000555405, ENST00000555537, ENST00000555763, ENST00000555961, ENST00000556170, ENST00000557026, ENST00000557673
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2407 2524 1676 580 1594 422 4341 2081 3092 378 1441 1603 174 1 1204 2786 6 2
Low 32 467 50 44 357 43 15 116 642 41 19 10 1 2
Below cutoff 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_051093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001329237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001329238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_033116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005268209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB082526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC007055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL049780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL117502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY048580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY080896 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC093881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC112101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM976692 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CF890866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB455229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000238616   ⟹   ENSP00000238616
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,079,353 - 75,127,048 (-)Ensembl
RefSeq Acc Id: ENST00000553823   ⟹   ENSP00000452537
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,118,887 - 75,127,344 (-)Ensembl
RefSeq Acc Id: ENST00000553945   ⟹   ENSP00000452544
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,120,516 - 75,127,053 (-)Ensembl
RefSeq Acc Id: ENST00000554258   ⟹   ENSP00000451604
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,117,213 - 75,126,933 (-)Ensembl
RefSeq Acc Id: ENST00000555405
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,082,121 - 75,091,685 (-)Ensembl
RefSeq Acc Id: ENST00000555537
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,096,670 - 75,101,065 (-)Ensembl
RefSeq Acc Id: ENST00000555763
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,084,087 - 75,085,095 (-)Ensembl
RefSeq Acc Id: ENST00000555961
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,118,869 - 75,120,730 (-)Ensembl
RefSeq Acc Id: ENST00000556170
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,086,429 - 75,127,045 (-)Ensembl
RefSeq Acc Id: ENST00000557026
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,082,121 - 75,117,245 (-)Ensembl
RefSeq Acc Id: ENST00000557673   ⟹   ENSP00000450943
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,117,217 - 75,127,040 (-)Ensembl
RefSeq Acc Id: ENST00000676476
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,099,027 - 75,106,091 (-)Ensembl
RefSeq Acc Id: ENST00000676711
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,082,172 - 75,106,262 (-)Ensembl
RefSeq Acc Id: ENST00000677411
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,108,270 - 75,127,047 (-)Ensembl
RefSeq Acc Id: ENST00000677700   ⟹   ENSP00000503940
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,082,129 - 75,113,405 (-)Ensembl
RefSeq Acc Id: ENST00000678037   ⟹   ENSP00000504620
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,081,411 - 75,126,964 (-)Ensembl
RefSeq Acc Id: ENST00000678531   ⟹   ENSP00000503827
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,081,411 - 75,127,040 (-)Ensembl
RefSeq Acc Id: ENST00000678749   ⟹   ENSP00000504104
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1475,082,119 - 75,127,344 (-)Ensembl
RefSeq Acc Id: NM_001329237   ⟹   NP_001316166
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,079,353 - 75,127,048 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001329238   ⟹   NP_001316167
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,079,353 - 75,127,048 (-)NCBI
Sequence:
RefSeq Acc Id: NM_033116   ⟹   NP_149107
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,079,353 - 75,127,048 (-)NCBI
GRCh371475,548,818 - 75,593,778 (-)ENTREZGENE
Build 361474,620,728 - 74,663,389 (-)NCBI Archive
HuRef1455,716,982 - 55,761,929 (-)ENTREZGENE
CHM1_11475,486,591 - 75,531,543 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005268209   ⟹   XP_005268266
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,082,115 - 75,127,061 (-)NCBI
GRCh371475,548,818 - 75,593,778 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024449741   ⟹   XP_024305509
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,082,115 - 75,127,637 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_149107   ⟸   NM_033116
- Peptide Label: isoform 2
- UniProtKB: Q8TD19 (UniProtKB/Swiss-Prot),   Q6PKF2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005268266   ⟸   XM_005268209
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: NP_001316167   ⟸   NM_001329238
- Peptide Label: isoform 3
- UniProtKB: Q8TD19 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001316166   ⟸   NM_001329237
- Peptide Label: isoform 1
- UniProtKB: Q8TD19 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_024305509   ⟸   XM_024449741
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000450943   ⟸   ENST00000557673
RefSeq Acc Id: ENSP00000238616   ⟸   ENST00000238616
RefSeq Acc Id: ENSP00000452537   ⟸   ENST00000553823
RefSeq Acc Id: ENSP00000452544   ⟸   ENST00000553945
RefSeq Acc Id: ENSP00000451604   ⟸   ENST00000554258
RefSeq Acc Id: ENSP00000503940   ⟸   ENST00000677700
RefSeq Acc Id: ENSP00000504620   ⟸   ENST00000678037
RefSeq Acc Id: ENSP00000504104   ⟸   ENST00000678749
RefSeq Acc Id: ENSP00000503827   ⟸   ENST00000678531
Protein Domains
Protein kinase

Promoters
RGD ID:6791761
Promoter ID:HG_KWN:19811
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_033116
Position:
Human AssemblyChrPosition (strand)Source
Build 361474,663,401 - 74,664,517 (-)MPROMDB
RGD ID:7228173
Promoter ID:EPDNEW_H19832
Type:initiation region
Name:NEK9_1
Description:NIMA related kinase 9
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,127,048 - 75,127,108EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q24.3(chr14:73877072-78042422)x1 copy number loss See cases [RCV000051548] Chr14:73877072..78042422 [GRCh38]
Chr14:74343775..78508765 [GRCh37]
Chr14:73413528..77578518 [NCBI36]
Chr14:14q24.3
pathogenic
GRCh38/hg38 14q24.2-32.2(chr14:72787506-99596719)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|See cases [RCV000052293] Chr14:72787506..99596719 [GRCh38]
Chr14:73254214..100063056 [GRCh37]
Chr14:72323967..99132809 [NCBI36]
Chr14:14q24.2-32.2
pathogenic
NM_033116.6(NEK9):c.2335C>T (p.Arg779Ter) single nucleotide variant Arthrogryposis, perthes disease, and upward gaze palsy [RCV001333413] Chr14:75091377 [GRCh38]
Chr14:75558080 [GRCh37]
Chr14:14q24.3
pathogenic
GRCh37/hg19 14q24.2-q24.3(chr14:73152115..77698582) deletion Intellectual disability, mild [RCV000190520] Chr14:73152115..77698582 [GRCh37]
Chr14:14q24.2-24.3
pathogenic|likely pathogenic
NM_033116.6(NEK9):c.1756dup (p.Thr586fs) duplication Malignant tumor of prostate [RCV000149323] Chr14:75101740..75101741 [GRCh38]
Chr14:75568443..75568444 [GRCh37]
Chr14:14q24.3
uncertain significance
GRCh38/hg38 14q24.1-31.1(chr14:69562099-81975384)x1 copy number loss See cases [RCV000134154] Chr14:69562099..81975384 [GRCh38]
Chr14:70028816..82441728 [GRCh37]
Chr14:69098569..81511481 [NCBI36]
Chr14:14q24.1-31.1
pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3 copy number gain See cases [RCV000134000] Chr14:73655772..106879298 [GRCh38]
Chr14:74122475..107287505 [GRCh37]
Chr14:73192228..106358550 [NCBI36]
Chr14:14q24.3-32.33
pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33
pathogenic
GRCh38/hg38 14q24.3(chr14:74986195-76399258)x1 copy number loss See cases [RCV000137114] Chr14:74986195..76399258 [GRCh38]
Chr14:75452898..76865601 [GRCh37]
Chr14:74522651..75935354 [NCBI36]
Chr14:14q24.3
uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33
pathogenic
GRCh38/hg38 14q24.3-31.1(chr14:73343213-78835059)x1 copy number loss See cases [RCV000143265] Chr14:73343213..78835059 [GRCh38]
Chr14:73809921..79301402 [GRCh37]
Chr14:72879674..78371155 [NCBI36]
Chr14:14q24.3-31.1
pathogenic|likely pathogenic
NM_033116.6(NEK9):c.500T>C (p.Ile167Thr) single nucleotide variant Nevus comedonicus [RCV000240653] Chr14:75120534 [GRCh38]
Chr14:75587237 [GRCh37]
Chr14:14q24.3
pathogenic
NM_033116.6(NEK9):c.1489C>T (p.Arg497Ter) single nucleotide variant Lethal congenital contracture syndrome 10 [RCV000234925] Chr14:75106541 [GRCh38]
Chr14:75573244 [GRCh37]
Chr14:14q24.3
pathogenic
NM_033116.6(NEK9):c.2042G>A (p.Arg681His) single nucleotide variant Arthrogryposis, perthes disease, and upward gaze palsy [RCV000234928] Chr14:75097231 [GRCh38]
Chr14:75563934 [GRCh37]
Chr14:14q24.3
pathogenic
NEK9, GLY572VAL AND IVS14, G-T, +1 single nucleotide variant NEVUS COMEDONICUS [RCV000234965]|Nevus comedonicus [RCV000234965]   pathogenic
NM_033116.4(NEK9):c.1817T>C (p.Ile573Thr) single nucleotide variant Nevus comedonicus [RCV000234968] Chr14:75103855 [GRCh38]
Chr14:75570558 [GRCh37]
Chr14:14q24.3
pathogenic
NM_033116.6(NEK9):c.727G>T (p.Glu243Ter) single nucleotide variant not provided [RCV000413100] Chr14:75117230 [GRCh38]
Chr14:75583933 [GRCh37]
Chr14:14q24.3
likely pathogenic
NM_033116.6(NEK9):c.908T>C (p.Leu303Pro) single nucleotide variant not provided [RCV000414495] Chr14:75113369 [GRCh38]
Chr14:75580072 [GRCh37]
Chr14:14q24.3
likely pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3 copy number gain See cases [RCV000448557] Chr14:62493932..107285437 [GRCh37]
Chr14:14q23.2-32.33
pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3 copy number gain See cases [RCV000512497] Chr14:73750741..107285437 [GRCh37]
Chr14:14q24.2-32.33
pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33
pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
NM_033116.6(NEK9):c.1050T>C (p.Tyr350=) single nucleotide variant not provided [RCV000960605] Chr14:75109817 [GRCh38]
Chr14:75576520 [GRCh37]
Chr14:14q24.3
benign
NM_033116.6(NEK9):c.2886A>C (p.Leu962Phe) single nucleotide variant not provided [RCV000881542] Chr14:75084618 [GRCh38]
Chr14:75551321 [GRCh37]
Chr14:14q24.3
benign
NM_033116.6(NEK9):c.59G>A (p.Ser20Asn) single nucleotide variant not provided [RCV000900787] Chr14:75126863 [GRCh38]
Chr14:75593566 [GRCh37]
Chr14:14q24.3
likely benign
NM_033116.6(NEK9):c.2442+4A>G single nucleotide variant not provided [RCV000881758] Chr14:75091266 [GRCh38]
Chr14:75557969 [GRCh37]
Chr14:14q24.3
likely benign
NM_033116.6(NEK9):c.250G>A (p.Asp84Asn) single nucleotide variant not provided [RCV000904745] Chr14:75124193 [GRCh38]
Chr14:75590896 [GRCh37]
Chr14:14q24.3
likely benign
NM_033116.6(NEK9):c.2271C>T (p.Gly757=) single nucleotide variant not provided [RCV000898737] Chr14:75091441 [GRCh38]
Chr14:75558144 [GRCh37]
Chr14:14q24.3
benign
NM_033116.6(NEK9):c.84G>C (p.Ser28=) single nucleotide variant not provided [RCV000904002] Chr14:75126838 [GRCh38]
Chr14:75593541 [GRCh37]
Chr14:14q24.3
likely benign
NM_033116.6(NEK9):c.2385A>G (p.Thr795=) single nucleotide variant not provided [RCV000885075] Chr14:75091327 [GRCh38]
Chr14:75558030 [GRCh37]
Chr14:14q24.3
likely benign
NM_033116.6(NEK9):c.128G>C (p.Gly43Ala) single nucleotide variant not provided [RCV000947580] Chr14:75126794 [GRCh38]
Chr14:75593497 [GRCh37]
Chr14:14q24.3
benign
GRCh37/hg19 14q24.3(chr14:74040231-76368547) copy number loss not provided [RCV000767572] Chr14:74040231..76368547 [GRCh37]
Chr14:14q24.3
likely pathogenic
NM_033116.6(NEK9):c.2482C>A (p.Pro828Thr) single nucleotide variant not provided [RCV000901111] Chr14:75088602 [GRCh38]
Chr14:75555305 [GRCh37]
Chr14:14q24.3
benign
NM_033116.6(NEK9):c.525-12dup duplication not provided [RCV000901112] Chr14:75118938..75118939 [GRCh38]
Chr14:75585641..75585642 [GRCh37]
Chr14:14q24.3
benign
NM_033116.6(NEK9):c.264G>C (p.Leu88=) single nucleotide variant not provided [RCV000917916] Chr14:75124179 [GRCh38]
Chr14:75590882 [GRCh37]
Chr14:14q24.3
benign
NM_033116.6(NEK9):c.1236C>T (p.Ala412=) single nucleotide variant not provided [RCV000895533] Chr14:75107434 [GRCh38]
Chr14:75574137 [GRCh37]
Chr14:14q24.3
likely benign
NM_033116.6(NEK9):c.190G>A (p.Gly64Arg) single nucleotide variant Lethal congenital contracture syndrome 10 [RCV001030010] Chr14:75126732 [GRCh38]
Chr14:75593435 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_033116.6(NEK9):c.1505A>G (p.Tyr502Cys) single nucleotide variant Retinopathy [RCV000845273] Chr14:75106525 [GRCh38]
Chr14:75573228 [GRCh37]
Chr14:14q24.3
likely benign
NM_033116.6(NEK9):c.486A>G (p.Ser162=) single nucleotide variant not provided [RCV000887989] Chr14:75120548 [GRCh38]
Chr14:75587251 [GRCh37]
Chr14:14q24.3
likely benign
NM_033116.6(NEK9):c.2232T>C (p.Thr744=) single nucleotide variant Arthrogryposis, perthes disease, and upward gaze palsy [RCV001336840]|not provided [RCV000884036] Chr14:75095373 [GRCh38]
Chr14:75562076 [GRCh37]
Chr14:14q24.3
likely benign|uncertain significance
NM_033116.6(NEK9):c.222T>C (p.Asp74=) single nucleotide variant not provided [RCV000910174] Chr14:75124221 [GRCh38]
Chr14:75590924 [GRCh37]
Chr14:14q24.3
benign
NM_033116.6(NEK9):c.2357G>A (p.Arg786Gln) single nucleotide variant not provided [RCV000890249] Chr14:75091355 [GRCh38]
Chr14:75558058 [GRCh37]
Chr14:14q24.3
benign
NM_033116.6(NEK9):c.762+10C>T single nucleotide variant Arthrogryposis, perthes disease, and upward gaze palsy [RCV001333414] Chr14:75117185 [GRCh38]
Chr14:75583888 [GRCh37]
Chr14:14q24.3
uncertain significance
NM_033116.6(NEK9):c.1126G>A (p.Ala376Thr) single nucleotide variant Lethal congenital contracture syndrome 10 [RCV001262353] Chr14:75109741 [GRCh38]
Chr14:75576444 [GRCh37]
Chr14:14q24.3
likely benign
NM_033116.6(NEK9):c.1432del (p.Leu478fs) deletion not provided [RCV001268840] Chr14:75106598 [GRCh38]
Chr14:75573301 [GRCh37]
Chr14:14q24.3
pathogenic
NM_033116.6(NEK9):c.874-2A>G single nucleotide variant not provided [RCV001268841] Chr14:75113405 [GRCh38]
Chr14:75580108 [GRCh37]
Chr14:14q24.3
likely pathogenic
NM_033116.6(NEK9):c.1327+1G>T single nucleotide variant Arthrogryposis, perthes disease, and upward gaze palsy [RCV001332756] Chr14:75107342 [GRCh38]
Chr14:75574045 [GRCh37]
Chr14:14q24.3
likely pathogenic
NM_033116.6(NEK9):c.1450C>T (p.Gln484Ter) single nucleotide variant Arthrogryposis, perthes disease, and upward gaze palsy [RCV001336839] Chr14:75106580 [GRCh38]
Chr14:75573283 [GRCh37]
Chr14:14q24.3
pathogenic
GRCh37/hg19 14q22.2-24.3(chr14:54654001-75828024)x3 copy number gain 14q22.2q24.3 duplication [RCV001506967] Chr14:54654001..75828024 [GRCh37]
Chr14:14q22.2-24.3
likely pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:18591 AgrOrtholog
COSMIC NEK9 COSMIC
Ensembl Genes ENSG00000119638 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000238616 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000450943 UniProtKB/TrEMBL
  ENSP00000451604 UniProtKB/TrEMBL
  ENSP00000452537 UniProtKB/TrEMBL
  ENSP00000452544 UniProtKB/TrEMBL
  ENSP00000503827 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000503940 UniProtKB/TrEMBL
  ENSP00000504104 UniProtKB/TrEMBL
  ENSP00000504620 ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENST00000238616 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000553823 UniProtKB/TrEMBL
  ENST00000553945 UniProtKB/TrEMBL
  ENST00000554258 UniProtKB/TrEMBL
  ENST00000557026 ENTREZGENE
  ENST00000557673 UniProtKB/TrEMBL
  ENST00000677700 UniProtKB/TrEMBL
  ENST00000678037 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000678531 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000678749 UniProtKB/TrEMBL
Gene3D-CATH 2.130.10.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000119638 GTEx
HGNC ID HGNC:18591 ENTREZGENE
Human Proteome Map NEK9 Human Proteome Map
InterPro Kinase-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nek9_STKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_kinase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RCC1/BLIP-II UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Reg_chr_condens UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ser/Thr_kinase_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:91754 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 91754 ENTREZGENE
OMIM 609798 OMIM
  614262 OMIM
  617022 OMIM
  617025 OMIM
Pfam Pkinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RCC1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA38593 PharmGKB
PRINTS RCCNDNSATION UniProtKB/TrEMBL
PROSITE PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_ST UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RCC1_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART S_TKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50985 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF56112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R6D1_HUMAN UniProtKB/TrEMBL
  A0A7I2V454_HUMAN UniProtKB/TrEMBL
  A0A7I2V4E9_HUMAN UniProtKB/TrEMBL
  A0A7I2V5R1_HUMAN UniProtKB/TrEMBL
  G3V2Z5_HUMAN UniProtKB/TrEMBL
  G3V459_HUMAN UniProtKB/TrEMBL
  G3V5V0_HUMAN UniProtKB/TrEMBL
  G3V5V6_HUMAN UniProtKB/TrEMBL
  L8EAL4_HUMAN UniProtKB/TrEMBL
  NEK9_HUMAN UniProtKB/Swiss-Prot
  Q6PKF2 ENTREZGENE, UniProtKB/TrEMBL
  Q8TD19 ENTREZGENE
UniProt Secondary Q52LK6 UniProtKB/Swiss-Prot
  Q8NCN0 UniProtKB/Swiss-Prot
  Q8TCY4 UniProtKB/Swiss-Prot
  Q9UPI4 UniProtKB/Swiss-Prot
  Q9Y6S4 UniProtKB/Swiss-Prot
  Q9Y6S5 UniProtKB/Swiss-Prot
  Q9Y6S6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-19 NEK9  NIMA related kinase 9    NIMA-related kinase 9  Symbol and/or name change 5135510 APPROVED
2012-11-20 NEK9  NIMA-related kinase 9    NIMA (never in mitosis gene a)- related kinase 9  Symbol and/or name change 5135510 APPROVED