KIF18A (kinesin family member 18A) - Rat Genome Database

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Gene: KIF18A (kinesin family member 18A) Homo sapiens
Analyze
Symbol: KIF18A
Name: kinesin family member 18A
RGD ID: 1352766
HGNC Page HGNC:29441
Description: Enables cytoskeletal protein binding activity; plus-end-directed microtubule motor activity; and tubulin-dependent ATPase activity. Involved in microtubule depolymerization and mitotic metaphase chromosome alignment. Located in several cellular components, including caveola; kinetochore microtubule; and ruffle. Biomarker of colorectal cancer and stomach cancer.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DKFZp434G2226; kinesin-like protein KIF18A; MS-KIF18A; PPP1R99
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381128,020,619 - 28,108,156 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1128,020,619 - 28,108,156 (-)EnsemblGRCh38hg38GRCh38
GRCh371128,042,166 - 28,129,703 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361127,998,739 - 28,086,322 (-)NCBINCBI36Build 36hg18NCBI36
Build 341127,998,741 - 28,086,223NCBI
Celera1128,188,055 - 28,275,612 (-)NCBICelera
Cytogenetic Map11p14.1NCBI
HuRef1127,740,692 - 27,828,542 (-)NCBIHuRef
CHM1_11128,041,056 - 28,128,676 (-)NCBICHM1_1
T2T-CHM13v2.01128,161,289 - 28,248,842 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-epigallocatechin 3-gallate  (EXP)
1,1-dichloroethene  (ISO)
1,2-dimethylhydrazine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17beta-estradiol  (EXP,ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-butoxyethanol  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
3-methylcholanthrene  (ISO)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acrylamide  (ISO)
aflatoxin B1  (EXP,ISO)
all-trans-retinoic acid  (EXP)
amitrole  (ISO)
amphetamine  (ISO)
arsenite(3-)  (EXP)
azathioprine  (EXP)
benzo[a]pyrene diol epoxide I  (EXP)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
buta-1,3-diene  (ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
caffeine  (EXP)
calcitriol  (EXP)
cefaloridine  (ISO)
chlorpyrifos  (ISO)
choline  (ISO)
cisplatin  (EXP)
cobalt dichloride  (EXP)
copper(II) sulfate  (EXP)
coumestrol  (EXP)
CU-O LINKAGE  (EXP)
Cuprizon  (ISO)
cyclosporin A  (EXP,ISO)
dicrotophos  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
Enterolactone  (EXP)
ethanol  (ISO)
folic acid  (ISO)
FR900359  (EXP)
furan  (ISO)
gentamycin  (ISO)
glyphosate  (ISO)
hydrogen peroxide  (EXP)
hydroquinone  (EXP)
L-methionine  (ISO)
lead(0)  (EXP)
leflunomide  (EXP)
lidocaine  (ISO)
methimazole  (ISO)
N-Nitrosopyrrolidine  (EXP)
ochratoxin A  (EXP,ISO)
oxaliplatin  (ISO)
ozone  (ISO)
paracetamol  (EXP,ISO)
PCB138  (ISO)
perfluorooctanoic acid  (EXP)
phenanthridone  (EXP)
piroxicam  (EXP)
potassium chromate  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
propanal  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
rotenone  (ISO)
SB 431542  (EXP)
senecionine  (ISO)
silicon dioxide  (ISO)
silver atom  (ISO)
silver(0)  (ISO)
sodium arsenite  (ISO)
sophoraflavanone B  (ISO)
sulfadimethoxine  (ISO)
sulforaphane  (EXP)
sunitinib  (EXP)
testosterone  (EXP)
tetrachloromethane  (ISO)
thiram  (EXP)
topotecan  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
trimellitic anhydride  (ISO)
triphenyl phosphate  (EXP)
trovafloxacin  (ISO)
valproic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Kinesin 18A expression: clinical relevance to colorectal cancer progression. Nagahara M, etal., Int J Cancer. 2011 Dec 1;129(11):2543-52. doi: 10.1002/ijc.25916. Epub 2011 Jun 9.
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
6. [Expression of KIF18A in gastric cancer and its association with prognosis]. Wang L, etal., Zhonghua Wei Chang Wai Ke Za Zhi. 2016 May;19(5):585-9.
Additional References at PubMed
PMID:11076863   PMID:11230166   PMID:11256614   PMID:14702039   PMID:15231748   PMID:15489334   PMID:15489336   PMID:15878648   PMID:16344560   PMID:16381901   PMID:16565220   PMID:17006958  
PMID:17346968   PMID:18029348   PMID:18267093   PMID:18680169   PMID:19625775   PMID:20153196   PMID:20595236   PMID:21231887   PMID:21873635   PMID:21884977   PMID:21885282   PMID:22104080  
PMID:22595673   PMID:22623531   PMID:23288039   PMID:23746518   PMID:24366813   PMID:25048371   PMID:25208566   PMID:25281536   PMID:25281560   PMID:25431949   PMID:25884224   PMID:26186194  
PMID:26496610   PMID:26912793   PMID:26949251   PMID:27173435   PMID:27880917   PMID:28209915   PMID:28514442   PMID:29466986   PMID:29507755   PMID:29656893   PMID:30122526   PMID:30306428  
PMID:30344098   PMID:30655363   PMID:30804394   PMID:30817091   PMID:30907518   PMID:31451680   PMID:31586073   PMID:31677127   PMID:31772692   PMID:31977917   PMID:32076268   PMID:32094263  
PMID:32253833   PMID:32716640   PMID:33619254   PMID:33660365   PMID:33872988   PMID:33961781   PMID:34373451   PMID:34795231   PMID:35271311   PMID:35696571   PMID:35915203   PMID:35926461  
PMID:36424410   PMID:36543142   PMID:37071664   PMID:37499664   PMID:38372748   PMID:38446308   PMID:39331093  


Genomics

Comparative Map Data
KIF18A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381128,020,619 - 28,108,156 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1128,020,619 - 28,108,156 (-)EnsemblGRCh38hg38GRCh38
GRCh371128,042,166 - 28,129,703 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361127,998,739 - 28,086,322 (-)NCBINCBI36Build 36hg18NCBI36
Build 341127,998,741 - 28,086,223NCBI
Celera1128,188,055 - 28,275,612 (-)NCBICelera
Cytogenetic Map11p14.1NCBI
HuRef1127,740,692 - 27,828,542 (-)NCBIHuRef
CHM1_11128,041,056 - 28,128,676 (-)NCBICHM1_1
T2T-CHM13v2.01128,161,289 - 28,248,842 (-)NCBIT2T-CHM13v2.0
Kif18a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392109,111,165 - 109,172,094 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2109,111,083 - 109,172,092 (+)EnsemblGRCm39 Ensembl
GRCm382109,280,738 - 109,341,749 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2109,280,738 - 109,341,747 (+)EnsemblGRCm38mm10GRCm38
MGSCv372109,120,895 - 109,181,904 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362109,081,577 - 109,142,586 (+)NCBIMGSCv36mm8
Celera2110,441,710 - 110,502,913 (+)NCBICelera
Cytogenetic Map2E3NCBI
cM Map256.55NCBI
Kif18a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83116,219,007 - 116,279,378 (+)NCBIGRCr8
mRatBN7.2395,764,388 - 95,824,756 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl395,764,388 - 95,824,582 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx399,327,315 - 99,387,814 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03107,926,278 - 107,986,777 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03105,687,071 - 105,747,262 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03100,366,168 - 100,426,867 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3100,366,168 - 100,427,030 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03106,967,785 - 107,028,416 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4394,825,019 - 94,885,158 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera394,796,565 - 94,856,504 (+)NCBICelera
Cytogenetic Map3q34NCBI
Kif18a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554767,058,573 - 7,109,610 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554767,058,682 - 7,117,496 (-)NCBIChiLan1.0ChiLan1.0
KIF18A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2930,234,673 - 30,322,407 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11130,236,640 - 30,323,236 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01127,989,506 - 28,076,078 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11127,890,317 - 27,976,429 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1127,888,435 - 27,976,429 (-)Ensemblpanpan1.1panPan2
KIF18A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12148,497,752 - 48,574,930 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2148,498,087 - 48,565,651 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2147,996,571 - 48,074,757 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02149,642,091 - 49,720,944 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2149,641,761 - 49,720,876 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12148,644,615 - 48,722,982 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02148,795,947 - 48,874,039 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02149,391,450 - 49,469,640 (-)NCBIUU_Cfam_GSD_1.0
Kif18a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494736,048,853 - 36,118,133 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365339,173,715 - 9,239,931 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365339,173,739 - 9,242,928 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
KIF18A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl232,244,137 - 32,335,736 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1232,244,073 - 32,331,392 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2234,827,426 - 34,914,679 (+)NCBISscrofa10.2Sscrofa10.2susScr3
KIF18A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1137,003,325 - 37,088,705 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl137,003,357 - 37,088,640 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666038134,292,420 - 134,378,450 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Kif18a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476617,564,560 - 17,622,932 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476617,565,072 - 17,622,342 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in KIF18A
52 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11p14.3-12(chr11:22550115-38199159)x1 copy number loss See cases [RCV000052648] Chr11:22550115..38199159 [GRCh38]
Chr11:22571661..38220709 [GRCh37]
Chr11:22528237..38177285 [NCBI36]
Chr11:11p14.3-12		 pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3 copy number gain See cases [RCV000053613] Chr11:202758..31726224 [GRCh38]
Chr11:202758..31747772 [GRCh37]
Chr11:192758..31704348 [NCBI36]
Chr11:11p15.5-13		 pathogenic
NM_031217.3(KIF18A):c.564C>T (p.Val188=) single nucleotide variant Malignant melanoma [RCV000069312] Chr11:28091433 [GRCh38]
Chr11:28112980 [GRCh37]
Chr11:28069556 [NCBI36]
Chr11:11p14.1		 not provided
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
GRCh38/hg38 11p14.2-13(chr11:26368962-35252976)x1 copy number loss See cases [RCV000135295] Chr11:26368962..35252976 [GRCh38]
Chr11:26390509..35274523 [GRCh37]
Chr11:26347085..35231099 [NCBI36]
Chr11:11p14.2-13		 pathogenic
GRCh38/hg38 11p14.3-13(chr11:24595399-31096539)x3 copy number gain See cases [RCV000134877] Chr11:24595399..31096539 [GRCh38]
Chr11:24616945..31118086 [GRCh37]
Chr11:24573521..31074662 [NCBI36]
Chr11:11p14.3-13		 pathogenic
GRCh38/hg38 11p15.1-13(chr11:20079474-34463996)x1 copy number loss See cases [RCV000142499] Chr11:20079474..34463996 [GRCh38]
Chr11:20101020..34485543 [GRCh37]
Chr11:20057596..34442119 [NCBI36]
Chr11:11p15.1-13		 pathogenic
NM_031217.4(KIF18A):c.2102A>G (p.Gln701Arg) single nucleotide variant not specified [RCV004293638] Chr11:28036511 [GRCh38]
Chr11:28058058 [GRCh37]
Chr11:11p14.1		 uncertain significance
GRCh37/hg19 11p15.1-13(chr11:18536224-31923308)x1 copy number loss Aniridia 1 [RCV000420782] Chr11:18536224..31923308 [GRCh37]
Chr11:11p15.1-13		 pathogenic
GRCh37/hg19 11p15.1-13(chr11:21586131-33168232)x1 copy number loss Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome [RCV000435400] Chr11:21586131..33168232 [GRCh37]
Chr11:11p15.1-13		 pathogenic
GRCh37/hg19 11p14.1-13(chr11:27895487-34494489)x1 copy number loss See cases [RCV000448524] Chr11:27895487..34494489 [GRCh37]
Chr11:11p14.1-13		 pathogenic
GRCh37/hg19 11p14.2-11.12(chr11:26574629-50508019)x3 copy number gain See cases [RCV000448603] Chr11:26574629..50508019 [GRCh37]
Chr11:11p14.2-11.12		 pathogenic
GRCh37/hg19 11p14.3-13(chr11:25771208-35614978)x1 copy number loss See cases [RCV000512014] Chr11:25771208..35614978 [GRCh37]
Chr11:11p14.3-13		 pathogenic
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3 copy number gain See cases [RCV000511561] Chr11:230615..37698540 [GRCh37]
Chr11:11p15.5-12		 pathogenic
GRCh37/hg19 11p14.1-12(chr11:27588560-41770792)x1 copy number loss See cases [RCV000511434] Chr11:27588560..41770792 [GRCh37]
Chr11:11p14.1-12		 pathogenic|uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_031217.4(KIF18A):c.980T>C (p.Ile327Thr) single nucleotide variant not specified [RCV004295274] Chr11:28084726 [GRCh38]
Chr11:28106273 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1795T>A (p.Ser599Thr) single nucleotide variant not specified [RCV004329980] Chr11:28059079 [GRCh38]
Chr11:28080626 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.463A>G (p.Thr155Ala) single nucleotide variant not specified [RCV004315413] Chr11:28094663 [GRCh38]
Chr11:28116210 [GRCh37]
Chr11:11p14.1		 uncertain significance
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 copy number gain See cases [RCV000512477] Chr11:230615..31995219 [GRCh37]
Chr11:11p15.5-13		 pathogenic
GRCh37/hg19 11p14.3-14.1(chr11:25090108-28909131)x3 copy number gain not provided [RCV000683363] Chr11:25090108..28909131 [GRCh37]
Chr11:11p14.3-14.1		 uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p14.3-12(chr11:24469451-37524085)x1 copy number loss not provided [RCV000737457] Chr11:24469451..37524085 [GRCh37]
Chr11:11p14.3-12		 pathogenic
GRCh37/hg19 11p14.3-13(chr11:25196998-34196484)x1 copy number loss not provided [RCV000737466] Chr11:25196998..34196484 [GRCh37]
Chr11:11p14.3-13		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p14.2-13(chr11:27154853-33302474)x1 copy number loss not provided [RCV000749997] Chr11:27154853..33302474 [GRCh37]
Chr11:11p14.2-13		 pathogenic
NM_031217.4(KIF18A):c.2535C>T (p.Asp845=) single nucleotide variant not provided [RCV000948863] Chr11:28023820 [GRCh38]
Chr11:28045367 [GRCh37]
Chr11:11p14.1		 benign|likely benign
GRCh37/hg19 11p14.3-13(chr11:22079154-35597645)x1 copy number loss not provided [RCV000849589] Chr11:22079154..35597645 [GRCh37]
Chr11:11p14.3-13		 pathogenic
GRCh37/hg19 11p14.1(chr11:28055151-28348275)x1 copy number loss not provided [RCV001006399] Chr11:28055151..28348275 [GRCh37]
Chr11:11p14.1		 uncertain significance
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13		 pathogenic
NM_031217.4(KIF18A):c.649C>T (p.His217Tyr) single nucleotide variant not specified [RCV004321896] Chr11:28090667 [GRCh38]
Chr11:28112214 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2117C>T (p.Thr706Ile) single nucleotide variant not specified [RCV004321394] Chr11:28036496 [GRCh38]
Chr11:28058043 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2108T>C (p.Ile703Thr) single nucleotide variant not specified [RCV004286020] Chr11:28036505 [GRCh38]
Chr11:28058052 [GRCh37]
Chr11:11p14.1		 uncertain significance
GRCh37/hg19 11p15.3-13(chr11:11053978-34732891)x3 copy number gain not provided [RCV001006387] Chr11:11053978..34732891 [GRCh37]
Chr11:11p15.3-13		 pathogenic
GRCh37/hg19 11p14.1(chr11:28055151-28268659) copy number loss not specified [RCV002052919] Chr11:28055151..28268659 [GRCh37]
Chr11:11p14.1		 uncertain significance
GRCh37/hg19 11p14.1-13(chr11:27547893-31656604)x1 copy number loss not provided [RCV002265529] Chr11:27547893..31656604 [GRCh37]
Chr11:11p14.1-13		 not provided
GRCh37/hg19 11p14.1(chr11:27382897-29172035)x1 copy number loss See cases [RCV002292391] Chr11:27382897..29172035 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2357A>T (p.Gln786Leu) single nucleotide variant not specified [RCV004133301] Chr11:28036256 [GRCh38]
Chr11:28057803 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.214C>T (p.Leu72Phe) single nucleotide variant not specified [RCV004238757] Chr11:28097734 [GRCh38]
Chr11:28119281 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1580A>G (p.His527Arg) single nucleotide variant not specified [RCV004224650] Chr11:28069269 [GRCh38]
Chr11:28090816 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1469G>A (p.Arg490His) single nucleotide variant not specified [RCV004244019] Chr11:28069380 [GRCh38]
Chr11:28090927 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1096G>A (p.Val366Ile) single nucleotide variant not specified [RCV004181686] Chr11:28083222 [GRCh38]
Chr11:28104769 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1935G>C (p.Gln645His) single nucleotide variant not specified [RCV004159396] Chr11:28058939 [GRCh38]
Chr11:28080486 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.805G>A (p.Gly269Ser) single nucleotide variant not specified [RCV004184021] Chr11:28088616 [GRCh38]
Chr11:28110163 [GRCh37]
Chr11:11p14.1		 likely benign
NM_031217.4(KIF18A):c.1780A>C (p.Asn594His) single nucleotide variant not specified [RCV004117701] Chr11:28059094 [GRCh38]
Chr11:28080641 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2168T>C (p.Met723Thr) single nucleotide variant not specified [RCV004208098] Chr11:28036445 [GRCh38]
Chr11:28057992 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.198G>C (p.Lys66Asn) single nucleotide variant not specified [RCV004171897] Chr11:28097750 [GRCh38]
Chr11:28119297 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.518A>G (p.Asn173Ser) single nucleotide variant not specified [RCV004112384] Chr11:28091479 [GRCh38]
Chr11:28113026 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2039A>G (p.His680Arg) single nucleotide variant not specified [RCV004173214] Chr11:28036574 [GRCh38]
Chr11:28058121 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2648G>A (p.Ser883Asn) single nucleotide variant not specified [RCV004197842] Chr11:28021249 [GRCh38]
Chr11:28042796 [GRCh37]
Chr11:11p14.1		 likely benign
NM_031217.4(KIF18A):c.2016G>A (p.Met672Ile) single nucleotide variant not specified [RCV004132693] Chr11:28036597 [GRCh38]
Chr11:28058144 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1751A>G (p.Tyr584Cys) single nucleotide variant not specified [RCV004153215] Chr11:28059123 [GRCh38]
Chr11:28080670 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2539A>C (p.Asn847His) single nucleotide variant not specified [RCV004100107] Chr11:28023816 [GRCh38]
Chr11:28045363 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2150C>T (p.Pro717Leu) single nucleotide variant not specified [RCV004249002] Chr11:28036463 [GRCh38]
Chr11:28058010 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1010T>C (p.Val337Ala) single nucleotide variant not specified [RCV004266324] Chr11:28084696 [GRCh38]
Chr11:28106243 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1576G>A (p.Gly526Ser) single nucleotide variant not specified [RCV004361088] Chr11:28069273 [GRCh38]
Chr11:28090820 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2656A>G (p.Arg886Gly) single nucleotide variant not specified [RCV004338900] Chr11:28021241 [GRCh38]
Chr11:28042788 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2316A>G (p.Ile772Met) single nucleotide variant not specified [RCV004411895] Chr11:28036297 [GRCh38]
Chr11:28057844 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2645C>T (p.Pro882Leu) single nucleotide variant not provided [RCV000894067] Chr11:28021252 [GRCh38]
Chr11:28042799 [GRCh37]
Chr11:11p14.1		 benign
NM_031217.4(KIF18A):c.2213A>T (p.Asn738Ile) single nucleotide variant not specified [RCV004175295] Chr11:28036400 [GRCh38]
Chr11:28057947 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1886T>C (p.Leu629Pro) single nucleotide variant not specified [RCV004251279] Chr11:28058988 [GRCh38]
Chr11:28080535 [GRCh37]
Chr11:11p14.1		 likely benign
NM_031217.4(KIF18A):c.289A>G (p.Ile97Val) single nucleotide variant not specified [RCV004355392] Chr11:28097659 [GRCh38]
Chr11:28119206 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1041G>C (p.Lys347Asn) single nucleotide variant not specified [RCV004411887] Chr11:28084665 [GRCh38]
Chr11:28106212 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.10A>C (p.Thr4Pro) single nucleotide variant not specified [RCV004411888] Chr11:28097938 [GRCh38]
Chr11:28119485 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1424A>C (p.Lys475Thr) single nucleotide variant not specified [RCV004411889] Chr11:28077008 [GRCh38]
Chr11:28098555 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.803C>G (p.Ser268Cys) single nucleotide variant not specified [RCV004411899] Chr11:28088618 [GRCh38]
Chr11:28110165 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.748C>T (p.Arg250Cys) single nucleotide variant not specified [RCV004411898] Chr11:28088673 [GRCh38]
Chr11:28110220 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.456A>G (p.Ile152Met) single nucleotide variant not specified [RCV004411897] Chr11:28094670 [GRCh38]
Chr11:28116217 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.242A>C (p.Asp81Ala) single nucleotide variant not specified [RCV004411896] Chr11:28097706 [GRCh38]
Chr11:28119253 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2290G>A (p.Glu764Lys) single nucleotide variant not specified [RCV004411894] Chr11:28036323 [GRCh38]
Chr11:28057870 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2278G>A (p.Glu760Lys) single nucleotide variant not specified [RCV004411893] Chr11:28036335 [GRCh38]
Chr11:28057882 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.2126A>G (p.Asp709Gly) single nucleotide variant not specified [RCV004411892] Chr11:28036487 [GRCh38]
Chr11:28058034 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1627C>T (p.Leu543Phe) single nucleotide variant not specified [RCV004411891] Chr11:28062480 [GRCh38]
Chr11:28084027 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1487A>G (p.Lys496Arg) single nucleotide variant not specified [RCV004411890] Chr11:28069362 [GRCh38]
Chr11:28090909 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1108A>G (p.Ile370Val) single nucleotide variant not specified [RCV004631226] Chr11:28083210 [GRCh38]
Chr11:28104757 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1598A>G (p.Lys533Arg) single nucleotide variant not specified [RCV004631227] Chr11:28062509 [GRCh38]
Chr11:28084056 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.1616A>G (p.His539Arg) single nucleotide variant not specified [RCV004631228] Chr11:28062491 [GRCh38]
Chr11:28084038 [GRCh37]
Chr11:11p14.1		 uncertain significance
NM_031217.4(KIF18A):c.886G>A (p.Ala296Thr) single nucleotide variant not specified [RCV004631229] Chr11:28088535 [GRCh38]
Chr11:28110082 [GRCh37]
Chr11:11p14.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:307
Count of miRNA genes:254
Interacting mature miRNAs:265
Transcripts:ENST00000263181, ENST00000526288, ENST00000531047, ENST00000533466
Prediction methods: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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1576345LVC1_HLeft ventricular contractility QTL 1 (human)3.93Left ventricular contractility11797076733970767Human
2289313BW388_HBody weight QTL 388 (human)1.570.00356Body fat amountabdominal11443467130434671Human
597306233GWAS1402307_Hvaginal microbiome measurement QTL GWAS1402307 (human)0.00001vaginal microbiome measurement112804103528041036Human
597247422GWAS1343496_Hchronic lymphocytic leukemia QTL GWAS1343496 (human)0.000008leukocyte integrity trait (VT:0010898)112804965428049655Human
597107838GWAS1203912_Htestosterone measurement QTL GWAS1203912 (human)1e-10testosterone measurementserum testosterone level (CMO:0000568)112805616128056162Human
597191092GWAS1287166_Htestosterone measurement QTL GWAS1287166 (human)2e-09testosterone measurementserum testosterone level (CMO:0000568)112805616128056162Human
597427308GWAS1523382_Hurate measurement QTL GWAS1523382 (human)3e-08urate measurementblood uric acid level (CMO:0000501)112803208628032087Human
597189803GWAS1285877_Hfree androgen index QTL GWAS1285877 (human)3e-08free androgen index112805616128056162Human
1559107SCL32_HSerum cholesterol level QTL 32 (human)3.27Lipid levelLDL cholesterol11289243028892430Human
597067138GWAS1163212_Hdiastolic blood pressure QTL GWAS1163212 (human)0.0000008diastolic blood pressurediastolic blood pressure (CMO:0000005)112803641028036411Human
597615883GWAS1672743_Hankylosing spondylitis QTL GWAS1672743 (human)1e-11ankylosing spondylitis112802817328028174Human
1559104SCL15_HSerum cholesterol level QTL 15 (human)2.60.06Lipid levelhyperlipidemia susceptibility111589236841892368Human
1559113SCL31_HSerum cholesterol level QTL 31 (human)3.72Lipid levelLDL cholesterol11289243028892430Human

Markers in Region
G63410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371128,105,894 - 28,106,218UniSTSGRCh37
Build 361128,062,470 - 28,062,794RGDNCBI36
Celera1128,251,762 - 28,252,084RGD
Cytogenetic Map11p14.1UniSTS
HuRef1127,804,822 - 27,805,144UniSTS
TNG Radiation Hybrid Map1113515.0UniSTS
SHGC-145194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371128,121,507 - 28,121,806UniSTSGRCh37
Build 361128,078,083 - 28,078,382RGDNCBI36
Celera1128,267,374 - 28,267,673RGD
Cytogenetic Map11p14.1UniSTS
HuRef1127,820,431 - 27,820,730UniSTS
TNG Radiation Hybrid Map1113541.0UniSTS
G02275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371128,059,049 - 28,059,294UniSTSGRCh37
Build 361128,015,625 - 28,015,870RGDNCBI36
Celera1128,204,941 - 28,205,186RGD
Cytogenetic Map11p14.1UniSTS
HuRef1127,757,583 - 27,757,828UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2414 2780 2192 4908 1691 2321 6 594 1932 435 2269 7176 6369 53 3676 1 848 1740 1616 174 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_031217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054370094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB062483 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC023206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC090159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW770226 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY791349 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC026090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC035917 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC048347 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB080843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000263181   ⟹   ENSP00000263181
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1128,020,619 - 28,108,156 (-)Ensembl
Ensembl Acc Id: ENST00000526288
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1128,097,332 - 28,108,145 (-)Ensembl
Ensembl Acc Id: ENST00000531047
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1128,084,274 - 28,088,580 (-)Ensembl
Ensembl Acc Id: ENST00000533466
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1128,076,482 - 28,097,887 (-)Ensembl
RefSeq Acc Id: NM_031217   ⟹   NP_112494
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381128,020,619 - 28,108,156 (-)NCBI
GRCh371128,042,163 - 28,129,746 (-)ENTREZGENE
Build 361127,998,739 - 28,086,322 (-)NCBI Archive
HuRef1127,740,692 - 27,828,542 (-)ENTREZGENE
CHM1_11128,041,056 - 28,128,676 (-)NCBI
T2T-CHM13v2.01128,161,289 - 28,248,820 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017018379   ⟹   XP_016873868
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381128,020,619 - 28,108,156 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017018380   ⟹   XP_016873869
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381128,020,619 - 28,081,768 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054370093   ⟹   XP_054226068
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01128,161,289 - 28,248,842 (-)NCBI
RefSeq Acc Id: XM_054370094   ⟹   XP_054226069
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01128,161,289 - 28,222,437 (-)NCBI
RefSeq Acc Id: NP_112494   ⟸   NM_031217
- UniProtKB: Q86VS5 (UniProtKB/Swiss-Prot),   Q4VPE3 (UniProtKB/Swiss-Prot),   Q9H0F3 (UniProtKB/Swiss-Prot),   Q8NI77 (UniProtKB/Swiss-Prot),   B2R6H3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016873868   ⟸   XM_017018379
- Peptide Label: isoform X1
- UniProtKB: Q86VS5 (UniProtKB/Swiss-Prot),   Q4VPE3 (UniProtKB/Swiss-Prot),   Q9H0F3 (UniProtKB/Swiss-Prot),   Q8NI77 (UniProtKB/Swiss-Prot),   B2R6H3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016873869   ⟸   XM_017018380
- Peptide Label: isoform X2
- Sequence:
Ensembl Acc Id: ENSP00000263181   ⟸   ENST00000263181
RefSeq Acc Id: XP_054226068   ⟸   XM_054370093
- Peptide Label: isoform X1
- UniProtKB: Q8NI77 (UniProtKB/Swiss-Prot),   Q86VS5 (UniProtKB/Swiss-Prot),   Q4VPE3 (UniProtKB/Swiss-Prot),   Q9H0F3 (UniProtKB/Swiss-Prot),   B2R6H3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054226069   ⟸   XM_054370094
- Peptide Label: isoform X2
Protein Domains
Kinesin motor

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8NI77-F1-model_v2 AlphaFold Q8NI77 1-898 view protein structure

Promoters
RGD ID:6789228
Promoter ID:HG_KWN:12529
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:ENST00000403099,   ENST00000406787,   NM_001113528,   NM_031217,   NM_152636,   OTTHUMT00000318137,   UC001MSD.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361128,085,516 - 28,086,547 (-)MPROMDB
RGD ID:7219905
Promoter ID:EPDNEW_H15698
Type:initiation region
Name:KIF18A_1
Description:kinesin family member 18A
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
GRCh381128,108,134 - 28,108,194EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:29441 AgrOrtholog
COSMIC KIF18A COSMIC
Ensembl Genes ENSG00000121621 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000263181 ENTREZGENE
  ENST00000263181.7 UniProtKB/Swiss-Prot
Gene3D-CATH 3.40.850.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000121621 GTEx
HGNC ID HGNC:29441 ENTREZGENE
Human Proteome Map KIF18A Human Proteome Map
InterPro Kinesin-like_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Kinesin_motor_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Kinesin_motor_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Kinesin_motor_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:81930 UniProtKB/Swiss-Prot
NCBI Gene 81930 ENTREZGENE
OMIM 611271 OMIM
PANTHER CENTROMERE PROTEIN E UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KINESIN-LIKE PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Kinesin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134951326 PharmGKB
PRINTS KINESINHEAVY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE KINESIN_MOTOR_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KINESIN_MOTOR_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART KISc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B2R6H3 ENTREZGENE, UniProtKB/TrEMBL
  KI18A_HUMAN UniProtKB/Swiss-Prot
  Q4G194_HUMAN UniProtKB/TrEMBL
  Q4VPE3 ENTREZGENE
  Q86VS5 ENTREZGENE
  Q8NI77 ENTREZGENE
  Q9H0F3 ENTREZGENE
UniProt Secondary Q4VPE3 UniProtKB/Swiss-Prot
  Q86VS5 UniProtKB/Swiss-Prot
  Q9H0F3 UniProtKB/Swiss-Prot