KIF16B (kinesin family member 16B) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: KIF16B (kinesin family member 16B) Homo sapiens
Analyze
Symbol: KIF16B
Name: kinesin family member 16B
RGD ID: 1320877
HGNC Page HGNC:15869
Description: Enables phosphatidylinositol phosphate binding activity; phosphatidylinositol-3,4-bisphosphate binding activity; and plus-end-directed microtubule motor activity. Involved in several processes, including early endosome to late endosome transport; receptor catabolic process; and regulation of receptor recycling. Located in early endosome and spindle.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: C20orf23; chromosome 20 open reading frame 23; kinesin motor protein; kinesin-like protein KIF16B; KISC20ORF; SNX23; sorting nexin 23; sorting nexin-23; testis secretory sperm-binding protein Li 201a
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
GRCh382016,272,104 - 16,573,448 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2016,272,104 - 16,573,448 (-)EnsemblGRCh38hg38GRCh38
GRCh372016,252,749 - 16,554,093 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362016,200,749 - 16,502,078 (-)NCBINCBI36Build 36hg18NCBI36
Celera2016,327,872 - 16,629,179 (-)NCBICelera
Cytogenetic Map20p12.1NCBI
HuRef2016,214,467 - 16,516,712 (-)NCBIHuRef
CHM1_12016,252,472 - 16,554,080 (-)NCBICHM1_1
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10997877   PMID:11780052   PMID:12461558   PMID:12477932   PMID:14702039   PMID:15489334   PMID:15882625   PMID:16084724   PMID:16782399   PMID:17203973   PMID:17641687   PMID:18445686  
PMID:21139019   PMID:21873635   PMID:22357949   PMID:22449649   PMID:22558309   PMID:23006423   PMID:23749212   PMID:26496610   PMID:27107012   PMID:28514442   PMID:29507755   PMID:29568061  
PMID:29736960   PMID:29778605   PMID:30639242   PMID:30659120   PMID:31056421   PMID:31182584   PMID:31618441   PMID:32296183   PMID:32807901   PMID:32877691   PMID:33957083   PMID:33961781  
PMID:34079125   PMID:34369648   PMID:34432599   PMID:34709727   PMID:35384245   PMID:35944360   PMID:37689310   PMID:37696580  


Genomics

Comparative Map Data
KIF16B
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382016,272,104 - 16,573,448 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2016,272,104 - 16,573,448 (-)EnsemblGRCh38hg38GRCh38
GRCh372016,252,749 - 16,554,093 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362016,200,749 - 16,502,078 (-)NCBINCBI36Build 36hg18NCBI36
Celera2016,327,872 - 16,629,179 (-)NCBICelera
Cytogenetic Map20p12.1NCBI
HuRef2016,214,467 - 16,516,712 (-)NCBIHuRef
CHM1_12016,252,472 - 16,554,080 (-)NCBICHM1_1
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBIT2T-CHM13v2.0
Kif16b
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392142,459,399 - 142,743,535 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2142,459,394 - 142,743,451 (-)EnsemblGRCm39 Ensembl
GRCm382142,618,340 - 142,901,609 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2142,617,474 - 142,901,531 (-)EnsemblGRCm38mm10GRCm38
MGSCv372142,444,081 - 142,727,200 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362142,309,786 - 142,592,905 (-)NCBIMGSCv36mm8
Celera2143,799,300 - 144,080,607 (-)NCBICelera
Cytogenetic Map2G1NCBI
cM Map270.67NCBI
Kif16b
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83150,428,233 - 150,707,755 (-)NCBIGRCr8
mRatBN7.23129,974,692 - 130,254,194 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3129,974,800 - 130,254,019 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3133,858,582 - 134,149,362 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03142,442,587 - 142,733,395 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03140,145,790 - 140,436,578 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03136,596,621 - 136,936,809 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3136,657,480 - 136,936,674 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03143,103,727 - 143,381,598 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43130,967,515 - 131,250,402 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13130,874,500 - 131,130,642 (-)NCBI
Celera3128,908,978 - 129,180,308 (-)NCBICelera
Cytogenetic Map3q41NCBI
Kif16b
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541525,447,539 - 25,740,775 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541525,449,734 - 25,740,697 (-)NCBIChiLan1.0ChiLan1.0
KIF16B
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22117,158,926 - 17,461,659 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12017,155,768 - 17,458,469 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02016,229,429 - 16,532,735 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12016,210,821 - 16,512,618 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2016,210,821 - 16,512,618 (-)Ensemblpanpan1.1panPan2
KIF16B
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1246,260,558 - 6,576,544 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl246,261,553 - 6,575,845 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha246,126,588 - 6,442,971 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0246,666,622 - 6,989,878 (+)NCBIROS_Cfam_1.0
UMICH_Zoey_3.1246,276,871 - 6,576,736 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0246,372,345 - 6,688,664 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0246,648,582 - 6,963,507 (+)NCBIUU_Cfam_GSD_1.0
Kif16b
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024408640155,012,499 - 155,294,440 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364853,443,878 - 3,726,174 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364853,443,878 - 3,728,613 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
KIF16B
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1724,882,142 - 25,186,703 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11724,882,139 - 25,188,990 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21728,210,127 - 28,417,272 (-)NCBISscrofa10.2Sscrofa10.2susScr3
KIF16B
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1245,189,908 - 45,495,837 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl245,189,756 - 45,495,725 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660545,562,674 - 5,874,409 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Kif16b
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474117,424,335 - 17,750,531 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in KIF16B
95 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_024704.4(KIF16B):c.1303-28571A>T single nucleotide variant Lung cancer [RCV000101418] Chr20:16458553 [GRCh38]
Chr20:16439198 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.4(KIF16B):c.47+4657C>T single nucleotide variant Lung cancer [RCV000101419] Chr20:16568572 [GRCh38]
Chr20:16549217 [GRCh37]
Chr20:20p12.1
uncertain significance
GRCh38/hg38 20p13-11.21(chr20:89939-25697564)x3 copy number gain See cases [RCV000051227] Chr20:89939..25697564 [GRCh38]
Chr20:70580..25678200 [GRCh37]
Chr20:18580..25626200 [NCBI36]
Chr20:20p13-11.21
pathogenic
GRCh38/hg38 20p13-11.23(chr20:89939-19146279)x3 copy number gain See cases [RCV000051041] Chr20:89939..19146279 [GRCh38]
Chr20:70580..19126923 [GRCh37]
Chr20:18580..19074923 [NCBI36]
Chr20:20p13-11.23
pathogenic
GRCh38/hg38 20p12.1-11.23(chr20:13160260-17910332)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052740]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052740]|See cases [RCV000052740] Chr20:13160260..17910332 [GRCh38]
Chr20:13140907..17890976 [GRCh37]
Chr20:13088907..17838976 [NCBI36]
Chr20:20p12.1-11.23
pathogenic
GRCh38/hg38 20p13-11.23(chr20:89939-19071495)x3 copy number gain See cases [RCV000052995] Chr20:89939..19071495 [GRCh38]
Chr20:70580..19052139 [GRCh37]
Chr20:18580..19000139 [NCBI36]
Chr20:20p13-11.23
pathogenic
GRCh38/hg38 20p13-11.22(chr20:89939-21787252)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052996]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052996]|See cases [RCV000052996] Chr20:89939..21787252 [GRCh38]
Chr20:70580..21767890 [GRCh37]
Chr20:18580..21715890 [NCBI36]
Chr20:20p13-11.22
pathogenic
GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3 copy number gain See cases [RCV000052999] Chr20:9811433..39316956 [GRCh38]
Chr20:9792081..37945599 [GRCh37]
Chr20:9740081..37379013 [NCBI36]
Chr20:20p12.2-q12
pathogenic
NM_024704.4(KIF16B):c.3864G>A (p.Val1288=) single nucleotide variant Malignant melanoma [RCV000072537] Chr20:16273343 [GRCh38]
Chr20:16253988 [GRCh37]
Chr20:16201988 [NCBI36]
Chr20:20p12.1
not provided
NM_001199866.1(KIF16B):c.3862C>T (p.Arg1288Ter) single nucleotide variant Malignant melanoma [RCV000072538] Chr20:16367463 [GRCh38]
Chr20:16348108 [GRCh37]
Chr20:16296108 [NCBI36]
Chr20:20p12.1
not provided
NM_024704.4(KIF16B):c.1377C>T (p.Ile459=) single nucleotide variant Malignant melanoma [RCV000063688] Chr20:16429908 [GRCh38]
Chr20:16410553 [GRCh37]
Chr20:16358553 [NCBI36]
Chr20:20p12.1
not provided
NM_024704.5(KIF16B):c.1588G>A (p.Val530Met) single nucleotide variant Malignant tumor of prostate [RCV000149101] Chr20:16427128 [GRCh38]
Chr20:16407773 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1979G>A (p.Arg660His) single nucleotide variant Malignant tumor of prostate [RCV000149102] Chr20:16380023 [GRCh38]
Chr20:16360668 [GRCh37]
Chr20:20p12.1
uncertain significance
GRCh38/hg38 20p13-q11.1(chr20:80106-30227427)x3 copy number gain See cases [RCV000133996] Chr20:80106..30227427 [GRCh38]
Chr20:60747..29462103 [GRCh37]
Chr20:8747..28075764 [NCBI36]
Chr20:20p13-q11.1
pathogenic
GRCh38/hg38 20p12.1(chr20:16073090-16628731)x3 copy number gain See cases [RCV000135136] Chr20:16073090..16628731 [GRCh38]
Chr20:16053735..16609376 [GRCh37]
Chr20:16001735..16557376 [NCBI36]
Chr20:20p12.1
benign
GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3 copy number gain See cases [RCV000135859] Chr20:99557..64277321 [GRCh38]
Chr20:80198..62908674 [GRCh37]
Chr20:28198..62379118 [NCBI36]
Chr20:20p13-q13.33
pathogenic
GRCh38/hg38 20p13-11.1(chr20:80927-26324843)x3 copy number gain See cases [RCV000142017] Chr20:80927..26324843 [GRCh38]
Chr20:61568..26305479 [GRCh37]
Chr20:9568..26253479 [NCBI36]
Chr20:20p13-11.1
pathogenic
GRCh38/hg38 20p13-11.23(chr20:80928-18688031)x3 copy number gain See cases [RCV000143426] Chr20:80928..18688031 [GRCh38]
Chr20:61569..18668675 [GRCh37]
Chr20:9569..18616675 [NCBI36]
Chr20:20p13-11.23
pathogenic
GRCh37/hg19 20p13-11.1(chr20:80198-26075841)x3 copy number gain See cases [RCV000239954] Chr20:80198..26075841 [GRCh37]
Chr20:20p13-11.1
pathogenic
GRCh37/hg19 20p12.1(chr20:15355046-16852195)x3 copy number gain See cases [RCV000446978] Chr20:15355046..16852195 [GRCh37]
Chr20:20p12.1
uncertain significance
GRCh37/hg19 20p12.3-12.1(chr20:9121901-16858469)x1 copy number loss See cases [RCV000448674] Chr20:9121901..16858469 [GRCh37]
Chr20:20p12.3-12.1
pathogenic
GRCh37/hg19 20p13-q11.21(chr20:80198-26208081)x3 copy number gain not provided [RCV000487461] Chr20:80198..26208081 [GRCh37]
Chr20:20p13-q11.21
pathogenic
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3 copy number gain See cases [RCV000510832] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33
pathogenic
NM_024704.5(KIF16B):c.1981C>T (p.Arg661Cys) single nucleotide variant Inborn genetic diseases [RCV003257137] Chr20:16380021 [GRCh38]
Chr20:16360666 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2118A>C (p.Gln706His) single nucleotide variant Inborn genetic diseases [RCV003285900] Chr20:16379884 [GRCh38]
Chr20:16360529 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1629G>C (p.Leu543Phe) single nucleotide variant Inborn genetic diseases [RCV003271596] Chr20:16406440 [GRCh38]
Chr20:16387085 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3498+2939C>A single nucleotide variant Inborn genetic diseases [RCV003299274] Chr20:16367647 [GRCh38]
Chr20:16348292 [GRCh37]
Chr20:20p12.1
uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555) copy number gain See cases [RCV000512450] Chr20:61569..62915555 [GRCh37]
Chr20:20p13-q13.33
pathogenic
NM_024704.5(KIF16B):c.3572A>G (p.Tyr1191Cys) single nucleotide variant not provided [RCV000512705] Chr20:16356379 [GRCh38]
Chr20:16337024 [GRCh37]
Chr20:20p12.1
uncertain significance
GRCh37/hg19 20p13-12.1(chr20:3092739-17091453)x1 copy number loss not provided [RCV000684134] Chr20:3092739..17091453 [GRCh37]
Chr20:20p13-12.1
pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62948788)x3 copy number gain not provided [RCV000741058] Chr20:63244..62948788 [GRCh37]
Chr20:20p13-q13.33
pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62961294)x3 copy number gain not provided [RCV000741059] Chr20:63244..62961294 [GRCh37]
Chr20:20p13-q13.33
pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3 copy number gain not provided [RCV000741057] Chr20:63244..62912463 [GRCh37]
Chr20:20p13-q13.33
pathogenic
NM_024704.5(KIF16B):c.2113G>A (p.Val705Ile) single nucleotide variant Inborn genetic diseases [RCV003243967] Chr20:16379889 [GRCh38]
Chr20:16360534 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1532C>T (p.Thr511Ile) single nucleotide variant Inborn genetic diseases [RCV003244159] Chr20:16427184 [GRCh38]
Chr20:16407829 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3611T>G (p.Phe1204Cys) single nucleotide variant not provided [RCV000991131] Chr20:16356340 [GRCh38]
Chr20:16336985 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3065A>G (p.His1022Arg) single nucleotide variant not provided [RCV000882964] Chr20:16378937 [GRCh38]
Chr20:16359582 [GRCh37]
Chr20:20p12.1
benign
GRCh37/hg19 20p12.1(chr20:15872280-16764799)x1 copy number loss not provided [RCV001007085] Chr20:15872280..16764799 [GRCh37]
Chr20:20p12.1
uncertain significance
GRCh37/hg19 20p12.2-11.23(chr20:11716825-19331055) copy number gain not provided [RCV000767743] Chr20:11716825..19331055 [GRCh37]
Chr20:20p12.2-11.23
pathogenic
NM_024704.5(KIF16B):c.3413G>A (p.Ser1138Asn) single nucleotide variant not provided [RCV000961691] Chr20:16371699 [GRCh38]
Chr20:16352344 [GRCh37]
Chr20:20p12.1
benign
NM_024704.5(KIF16B):c.1671C>T (p.Ala557=) single nucleotide variant not provided [RCV000943375] Chr20:16406398 [GRCh38]
Chr20:16387043 [GRCh37]
Chr20:20p12.1
likely benign
NM_024704.5(KIF16B):c.494A>G (p.Lys165Arg) single nucleotide variant not provided [RCV001092533] Chr20:16511480 [GRCh38]
Chr20:16492125 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.456A>G (p.Glu152=) single nucleotide variant not provided [RCV000968404] Chr20:16511518 [GRCh38]
Chr20:16492163 [GRCh37]
Chr20:20p12.1
benign
GRCh37/hg19 20p12.3-11.22(chr20:8571696-22088650)x1 copy number loss not provided [RCV001007080] Chr20:8571696..22088650 [GRCh37]
Chr20:20p12.3-11.22
pathogenic
NM_024704.5(KIF16B):c.1587C>T (p.Ile529=) single nucleotide variant not provided [RCV000958004] Chr20:16427129 [GRCh38]
Chr20:16407774 [GRCh37]
Chr20:20p12.1
benign
GRCh37/hg19 20p13-11.1(chr20:61568-26305479)x3 copy number gain not provided [RCV001007068] Chr20:61568..26305479 [GRCh37]
Chr20:20p13-11.1
pathogenic
NM_024704.5(KIF16B):c.2586G>T (p.Glu862Asp) single nucleotide variant Intellectual disability [RCV001263412] Chr20:16379416 [GRCh38]
Chr20:16360061 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2446G>A (p.Glu816Lys) single nucleotide variant Inborn genetic diseases [RCV002557961]|not provided [RCV001092532] Chr20:16379556 [GRCh38]
Chr20:16360201 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3550A>G (p.Ile1184Val) single nucleotide variant not provided [RCV001591684] Chr20:16356401 [GRCh38]
Chr20:16337046 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3773_3774del (p.Ala1258fs) deletion Muscular atrophy [RCV001543627] Chr20:16312356..16312357 [GRCh38]
Chr20:16293001..16293002 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3498+3074C>G single nucleotide variant not provided [RCV001091289] Chr20:16367512 [GRCh38]
Chr20:16348157 [GRCh37]
Chr20:20p12.1
likely benign
NM_024704.5(KIF16B):c.3481C>T (p.Arg1161Cys) single nucleotide variant not provided [RCV001091290] Chr20:16370603 [GRCh38]
Chr20:16351248 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2564A>G (p.Gln855Arg) single nucleotide variant See cases [RCV001291804] Chr20:16379438 [GRCh38]
Chr20:16360083 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1754A>C (p.Asn585Thr) single nucleotide variant not provided [RCV001839462] Chr20:16404843 [GRCh38]
Chr20:16385488 [GRCh37]
Chr20:20p12.1
uncertain significance
GRCh37/hg19 20p12.2-11.23(chr20:11702911-19179706)x3 copy number gain not provided [RCV001795841] Chr20:11702911..19179706 [GRCh37]
Chr20:20p12.2-11.23
uncertain significance
NM_024704.5(KIF16B):c.3098G>C (p.Arg1033Thr) single nucleotide variant Inborn genetic diseases [RCV002945390] Chr20:16378904 [GRCh38]
Chr20:16359549 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2661A>C (p.Glu887Asp) single nucleotide variant Inborn genetic diseases [RCV002686784] Chr20:16379341 [GRCh38]
Chr20:16359986 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3244G>A (p.Asp1082Asn) single nucleotide variant Inborn genetic diseases [RCV002684380] Chr20:16374363 [GRCh38]
Chr20:16355008 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3808G>A (p.Asp1270Asn) single nucleotide variant Inborn genetic diseases [RCV002727786] Chr20:16273399 [GRCh38]
Chr20:16254044 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3449A>G (p.Asp1150Gly) single nucleotide variant Inborn genetic diseases [RCV002883513] Chr20:16370635 [GRCh38]
Chr20:16351280 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2111G>A (p.Arg704His) single nucleotide variant Inborn genetic diseases [RCV002992757] Chr20:16379891 [GRCh38]
Chr20:16360536 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3498+3406C>T single nucleotide variant Inborn genetic diseases [RCV002689663] Chr20:16367180 [GRCh38]
Chr20:16347825 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1162G>A (p.Ala388Thr) single nucleotide variant Inborn genetic diseases [RCV002970274] Chr20:16504386 [GRCh38]
Chr20:16485031 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3062G>A (p.Arg1021Lys) single nucleotide variant Inborn genetic diseases [RCV002752275] Chr20:16378940 [GRCh38]
Chr20:16359585 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2847G>T (p.Met949Ile) single nucleotide variant Inborn genetic diseases [RCV002879840] Chr20:16379155 [GRCh38]
Chr20:16359800 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3607G>A (p.Glu1203Lys) single nucleotide variant Inborn genetic diseases [RCV002840073] Chr20:16356344 [GRCh38]
Chr20:16336989 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1040G>A (p.Ser347Asn) single nucleotide variant Inborn genetic diseases [RCV002972781] Chr20:16504508 [GRCh38]
Chr20:16485153 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1503G>C (p.Glu501Asp) single nucleotide variant Inborn genetic diseases [RCV002753627] Chr20:16427213 [GRCh38]
Chr20:16407858 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3498+3036T>C single nucleotide variant Inborn genetic diseases [RCV002762624] Chr20:16367550 [GRCh38]
Chr20:16348195 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2212G>T (p.Asp738Tyr) single nucleotide variant Inborn genetic diseases [RCV002660615] Chr20:16379790 [GRCh38]
Chr20:16360435 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2296G>A (p.Glu766Lys) single nucleotide variant Inborn genetic diseases [RCV002884413] Chr20:16379706 [GRCh38]
Chr20:16360351 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3752A>G (p.Asn1251Ser) single nucleotide variant Inborn genetic diseases [RCV002762145] Chr20:16312378 [GRCh38]
Chr20:16293023 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.241A>G (p.Thr81Ala) single nucleotide variant Inborn genetic diseases [RCV003000869] Chr20:16515655 [GRCh38]
Chr20:16496300 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3718G>T (p.Ala1240Ser) single nucleotide variant Inborn genetic diseases [RCV002844846] Chr20:16312412 [GRCh38]
Chr20:16293057 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1090A>G (p.Ile364Val) single nucleotide variant Inborn genetic diseases [RCV002799351] Chr20:16504458 [GRCh38]
Chr20:16485103 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3299G>A (p.Ser1100Asn) single nucleotide variant Inborn genetic diseases [RCV002781676] Chr20:16374308 [GRCh38]
Chr20:16354953 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3158T>G (p.Leu1053Arg) single nucleotide variant Inborn genetic diseases [RCV002925426] Chr20:16378844 [GRCh38]
Chr20:16359489 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.259G>A (p.Val87Met) single nucleotide variant Inborn genetic diseases [RCV002845906] Chr20:16515637 [GRCh38]
Chr20:16496282 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.244C>G (p.Leu82Val) single nucleotide variant Inborn genetic diseases [RCV002987107] Chr20:16515652 [GRCh38]
Chr20:16496297 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3498+2923A>G single nucleotide variant Inborn genetic diseases [RCV002708650] Chr20:16367663 [GRCh38]
Chr20:16348308 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.796G>A (p.Gly266Arg) single nucleotide variant Inborn genetic diseases [RCV002955001] Chr20:16506094 [GRCh38]
Chr20:16486739 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1106A>G (p.Asn369Ser) single nucleotide variant Inborn genetic diseases [RCV002893582] Chr20:16504442 [GRCh38]
Chr20:16485087 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2507T>C (p.Leu836Pro) single nucleotide variant Inborn genetic diseases [RCV002826705] Chr20:16379495 [GRCh38]
Chr20:16360140 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3659G>A (p.Arg1220His) single nucleotide variant Inborn genetic diseases [RCV002956704] Chr20:16335978 [GRCh38]
Chr20:16316623 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2597G>T (p.Cys866Phe) single nucleotide variant Inborn genetic diseases [RCV002698869] Chr20:16379405 [GRCh38]
Chr20:16360050 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.386T>C (p.Leu129Pro) single nucleotide variant Inborn genetic diseases [RCV002929297] Chr20:16512886 [GRCh38]
Chr20:16493531 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2791C>A (p.Leu931Ile) single nucleotide variant Inborn genetic diseases [RCV002805230] Chr20:16379211 [GRCh38]
Chr20:16359856 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1382A>G (p.Asp461Gly) single nucleotide variant Inborn genetic diseases [RCV002788509] Chr20:16429903 [GRCh38]
Chr20:16410548 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3076G>T (p.Gly1026Cys) single nucleotide variant Inborn genetic diseases [RCV002770054] Chr20:16378926 [GRCh38]
Chr20:16359571 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.637G>A (p.Ala213Thr) single nucleotide variant Inborn genetic diseases [RCV002832062] Chr20:16508020 [GRCh38]
Chr20:16488665 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3386G>A (p.Arg1129His) single nucleotide variant Inborn genetic diseases [RCV002921784] Chr20:16371726 [GRCh38]
Chr20:16352371 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.853G>A (p.Val285Ile) single nucleotide variant Inborn genetic diseases [RCV002809211] Chr20:16506037 [GRCh38]
Chr20:16486682 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3835G>A (p.Ala1279Thr) single nucleotide variant Inborn genetic diseases [RCV002673635] Chr20:16273372 [GRCh38]
Chr20:16254017 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2235A>T (p.Glu745Asp) single nucleotide variant Inborn genetic diseases [RCV002809633] Chr20:16379767 [GRCh38]
Chr20:16360412 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2339G>T (p.Arg780Leu) single nucleotide variant Inborn genetic diseases [RCV003203275] Chr20:16379663 [GRCh38]
Chr20:16360308 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1594G>A (p.Ala532Thr) single nucleotide variant Inborn genetic diseases [RCV003204902] Chr20:16427122 [GRCh38]
Chr20:16407767 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2594A>G (p.Lys865Arg) single nucleotide variant Inborn genetic diseases [RCV003191419] Chr20:16379408 [GRCh38]
Chr20:16360053 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2613A>C (p.Glu871Asp) single nucleotide variant Inborn genetic diseases [RCV003194893] Chr20:16379389 [GRCh38]
Chr20:16360034 [GRCh37]
Chr20:20p12.1
likely benign
NM_024704.5(KIF16B):c.3081G>A (p.Met1027Ile) single nucleotide variant Inborn genetic diseases [RCV003304066] Chr20:16378921 [GRCh38]
Chr20:16359566 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3898T>C (p.Phe1300Leu) single nucleotide variant Inborn genetic diseases [RCV003309415] Chr20:16273309 [GRCh38]
Chr20:16253954 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3556A>G (p.Ile1186Val) single nucleotide variant Inborn genetic diseases [RCV003308862] Chr20:16356395 [GRCh38]
Chr20:16337040 [GRCh37]
Chr20:20p12.1
uncertain significance
GRCh38/hg38 20p13-11.21(chr20:87153-23635465)x3 copy number gain Renal agenesis [RCV003327640] Chr20:87153..23635465 [GRCh38]
Chr20:20p13-11.21
pathogenic
NM_024704.5(KIF16B):c.2603A>G (p.His868Arg) single nucleotide variant Inborn genetic diseases [RCV003364589] Chr20:16379399 [GRCh38]
Chr20:16360044 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1808G>A (p.Arg603His) single nucleotide variant Inborn genetic diseases [RCV003349887] Chr20:16381724 [GRCh38]
Chr20:16362369 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2578A>G (p.Ile860Val) single nucleotide variant Inborn genetic diseases [RCV003346808] Chr20:16379424 [GRCh38]
Chr20:16360069 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.2686A>G (p.Lys896Glu) single nucleotide variant Inborn genetic diseases [RCV003347209] Chr20:16379316 [GRCh38]
Chr20:16359961 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1914G>T (p.Glu638Asp) single nucleotide variant Inborn genetic diseases [RCV003386807] Chr20:16380088 [GRCh38]
Chr20:16360733 [GRCh37]
Chr20:20p12.1
uncertain significance
GRCh37/hg19 20p13-11.21(chr20:68351-23860313)x3 copy number gain not provided [RCV003885495] Chr20:68351..23860313 [GRCh37]
Chr20:20p13-11.21
pathogenic
NM_024704.5(KIF16B):c.3351G>C (p.Arg1117Ser) single nucleotide variant not provided [RCV003886838] Chr20:16371761 [GRCh38]
Chr20:16352406 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.470G>A (p.Arg157His) single nucleotide variant Inborn genetic diseases [RCV003361302] Chr20:16511504 [GRCh38]
Chr20:16492149 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.3029C>A (p.Ala1010Asp) single nucleotide variant Inborn genetic diseases [RCV003204600] Chr20:16378973 [GRCh38]
Chr20:16359618 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.1213G>A (p.Glu405Lys) single nucleotide variant Inborn genetic diseases [RCV003359193] Chr20:16497642 [GRCh38]
Chr20:16478287 [GRCh37]
Chr20:20p12.1
uncertain significance
NM_024704.5(KIF16B):c.712T>A (p.Ser238Thr) single nucleotide variant Inborn genetic diseases [RCV003378644] Chr20:16506178 [GRCh38]
Chr20:16486823 [GRCh37]
Chr20:20p12.1
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2281
Count of miRNA genes:622
Interacting mature miRNAs:705
Transcripts:ENST00000354981, ENST00000355755, ENST00000378003, ENST00000408042, ENST00000450176
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.

Markers in Region
Z94492  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372016,268,282 - 16,268,378UniSTSGRCh37
Build 362016,216,282 - 16,216,378RGDNCBI36
Celera2016,343,405 - 16,343,501RGD
Cytogenetic Map20p11.23UniSTS
HuRef2016,230,036 - 16,230,132UniSTS
Z94570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372016,398,694 - 16,398,855UniSTSGRCh37
Build 362016,346,694 - 16,346,855RGDNCBI36
Celera2016,473,820 - 16,473,981RGD
Cytogenetic Map20p11.23UniSTS
HuRef2016,361,034 - 16,361,195UniSTS
WIAF-1621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372016,252,903 - 16,253,023UniSTSGRCh37
Build 362016,200,903 - 16,201,023RGDNCBI36
Celera2016,328,026 - 16,328,146RGD
Cytogenetic Map20p11.23UniSTS
HuRef2016,214,621 - 16,214,741UniSTS
GeneMap99-GB4 RH Map2086.2UniSTS
NCBI RH Map20125.1UniSTS
Z94444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372016,323,403 - 16,323,554UniSTSGRCh37
Build 362016,271,403 - 16,271,554RGDNCBI36
Celera2016,398,527 - 16,398,678RGD
Cytogenetic Map20p11.23UniSTS
HuRef2016,285,876 - 16,286,027UniSTS
Z94715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372016,477,589 - 16,477,739UniSTSGRCh37
Build 362016,425,589 - 16,425,739RGDNCBI36
Celera2016,552,694 - 16,552,844RGD
Cytogenetic Map20p11.23UniSTS
HuRef2016,440,102 - 16,440,252UniSTS
Z94615  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372016,382,114 - 16,382,259UniSTSGRCh37
Build 362016,330,114 - 16,330,259RGDNCBI36
Celera2016,457,240 - 16,457,385RGD
Cytogenetic Map20p11.23UniSTS
HuRef2016,344,412 - 16,344,557UniSTS
G18087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372016,510,597 - 16,510,714UniSTSGRCh37
Build 362016,458,597 - 16,458,714RGDNCBI36
Celera2016,585,701 - 16,585,818RGD
Cytogenetic Map20p11.23UniSTS
HuRef2016,473,217 - 16,473,334UniSTS
RH78581  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372016,252,987 - 16,253,072UniSTSGRCh37
Build 362016,200,987 - 16,201,072RGDNCBI36
Celera2016,328,110 - 16,328,195RGD
Cytogenetic Map20p11.23UniSTS
HuRef2016,214,705 - 16,214,790UniSTS
GeneMap99-GB4 RH Map2086.2UniSTS
NCBI RH Map20125.1UniSTS


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 490 202 479 38 177 41 1415 99 544 186 320 460 7 39 1009 2
Low 1948 2438 1247 586 1437 424 2942 2068 3187 233 1139 1150 167 1 1165 1779 4 2
Below cutoff 350 326 30 3 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_028043 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001199865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001199866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001410853 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_024704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260750 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260753 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005260755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006723588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047440266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323638 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323639 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054323646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB046810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK026698 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK095322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL049794 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL117376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL118509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY044654 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY166853 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC034984 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC050577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC110317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC150261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ067573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647572 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471133 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HM005614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456837 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF456843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000354981   ⟹   ENSP00000347076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2016,272,104 - 16,573,448 (-)Ensembl
RefSeq Acc Id: ENST00000355755   ⟹   ENSP00000347995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2016,273,253 - 16,371,763 (-)Ensembl
RefSeq Acc Id: ENST00000408042   ⟹   ENSP00000384164
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2016,366,843 - 16,573,433 (-)Ensembl
RefSeq Acc Id: ENST00000450176   ⟹   ENSP00000396264
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2016,379,750 - 16,404,867 (-)Ensembl
RefSeq Acc Id: ENST00000635823   ⟹   ENSP00000490639
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2016,366,843 - 16,573,382 (-)Ensembl
RefSeq Acc Id: ENST00000636835   ⟹   ENSP00000489838
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2016,272,104 - 16,573,434 (-)Ensembl
RefSeq Acc Id: NM_001199865   ⟹   NP_001186794
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
GRCh372016,252,742 - 16,554,079 (-)NCBI
HuRef2016,214,467 - 16,516,712 (-)ENTREZGENE
CHM1_12016,252,472 - 16,554,080 (-)NCBI
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001199866   ⟹   NP_001186795
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,366,843 - 16,573,448 (-)NCBI
GRCh372016,252,742 - 16,554,079 (-)NCBI
HuRef2016,214,467 - 16,516,712 (-)ENTREZGENE
CHM1_12016,347,217 - 16,554,080 (-)NCBI
T2T-CHM13v2.02016,417,795 - 16,624,561 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001410853   ⟹   NP_001397782
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,366,843 - 16,573,448 (-)NCBI
T2T-CHM13v2.02016,417,795 - 16,624,561 (-)NCBI
RefSeq Acc Id: NM_024704   ⟹   NP_078980
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
GRCh372016,252,742 - 16,554,079 (-)NCBI
Build 362016,200,749 - 16,502,078 (-)NCBI Archive
Celera2016,327,872 - 16,629,179 (-)RGD
HuRef2016,214,467 - 16,516,712 (-)ENTREZGENE
CHM1_12016,252,472 - 16,554,080 (-)NCBI
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005260750   ⟹   XP_005260807
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,366,928 - 16,573,448 (-)NCBI
GRCh372016,252,742 - 16,554,079 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005260751   ⟹   XP_005260808
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,366,928 - 16,573,448 (-)NCBI
GRCh372016,252,742 - 16,554,079 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005260753   ⟹   XP_005260810
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005260754   ⟹   XP_005260811
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005260755   ⟹   XP_005260812
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006723588   ⟹   XP_006723651
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017027926   ⟹   XP_016883415
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047440261   ⟹   XP_047296217
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,366,928 - 16,573,448 (-)NCBI
RefSeq Acc Id: XM_047440262   ⟹   XP_047296218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
RefSeq Acc Id: XM_047440263   ⟹   XP_047296219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
RefSeq Acc Id: XM_047440264   ⟹   XP_047296220
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
RefSeq Acc Id: XM_047440265   ⟹   XP_047296221
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
RefSeq Acc Id: XM_047440266   ⟹   XP_047296222
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382016,272,104 - 16,573,448 (-)NCBI
RefSeq Acc Id: XM_054323634   ⟹   XP_054179609
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,417,795 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323635   ⟹   XP_054179610
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,417,795 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323636   ⟹   XP_054179611
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,417,795 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323637   ⟹   XP_054179612
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323638   ⟹   XP_054179613
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323639   ⟹   XP_054179614
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323640   ⟹   XP_054179615
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323641   ⟹   XP_054179616
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323642   ⟹   XP_054179617
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323643   ⟹   XP_054179618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323644   ⟹   XP_054179619
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323645   ⟹   XP_054179620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
RefSeq Acc Id: XM_054323646   ⟹   XP_054179621
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02016,322,635 - 16,624,561 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001186794 (Get FASTA)   NCBI Sequence Viewer  
  NP_001186795 (Get FASTA)   NCBI Sequence Viewer  
  NP_001397782 (Get FASTA)   NCBI Sequence Viewer  
  NP_078980 (Get FASTA)   NCBI Sequence Viewer  
  XP_005260807 (Get FASTA)   NCBI Sequence Viewer  
  XP_005260808 (Get FASTA)   NCBI Sequence Viewer  
  XP_005260810 (Get FASTA)   NCBI Sequence Viewer  
  XP_005260811 (Get FASTA)   NCBI Sequence Viewer  
  XP_005260812 (Get FASTA)   NCBI Sequence Viewer  
  XP_006723651 (Get FASTA)   NCBI Sequence Viewer  
  XP_016883415 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296217 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296218 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296219 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296220 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296221 (Get FASTA)   NCBI Sequence Viewer  
  XP_047296222 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179609 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179610 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179611 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179612 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179613 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179614 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179615 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179616 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179617 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179618 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179619 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179620 (Get FASTA)   NCBI Sequence Viewer  
  XP_054179621 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH34984 (Get FASTA)   NCBI Sequence Viewer  
  AAI10318 (Get FASTA)   NCBI Sequence Viewer  
  AAI50262 (Get FASTA)   NCBI Sequence Viewer  
  AAK98768 (Get FASTA)   NCBI Sequence Viewer  
  AAO17292 (Get FASTA)   NCBI Sequence Viewer  
  AEE61211 (Get FASTA)   NCBI Sequence Viewer  
  BAA90971 (Get FASTA)   NCBI Sequence Viewer  
  BAB13416 (Get FASTA)   NCBI Sequence Viewer  
  BAB15530 (Get FASTA)   NCBI Sequence Viewer  
  CAI46105 (Get FASTA)   NCBI Sequence Viewer  
  CAI46266 (Get FASTA)   NCBI Sequence Viewer  
  EAX10287 (Get FASTA)   NCBI Sequence Viewer  
  EAX10288 (Get FASTA)   NCBI Sequence Viewer  
  EAX10289 (Get FASTA)   NCBI Sequence Viewer  
  EAX10290 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000347076
  ENSP00000347076.2
  ENSP00000384164
  ENSP00000384164.1
  ENSP00000396264.1
  ENSP00000489838
  ENSP00000489838.1
  ENSP00000490639
  ENSP00000490639.2
GenBank Protein Q96L93 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_078980   ⟸   NM_024704
- Peptide Label: isoform 2
- UniProtKB: B1AKT7 (UniProtKB/Swiss-Prot),   B1AKG3 (UniProtKB/Swiss-Prot),   A7E2A8 (UniProtKB/Swiss-Prot),   A6NKJ9 (UniProtKB/Swiss-Prot),   Q9HCI2 (UniProtKB/Swiss-Prot),   Q9H5U0 (UniProtKB/Swiss-Prot),   Q9BQM5 (UniProtKB/Swiss-Prot),   Q9BQM1 (UniProtKB/Swiss-Prot),   Q9BQM0 (UniProtKB/Swiss-Prot),   Q9BQJ8 (UniProtKB/Swiss-Prot),   Q8IYU0 (UniProtKB/Swiss-Prot),   Q86YS5 (UniProtKB/Swiss-Prot),   Q86VL9 (UniProtKB/Swiss-Prot),   Q5TFK5 (UniProtKB/Swiss-Prot),   Q5JWW3 (UniProtKB/Swiss-Prot),   Q5HYK1 (UniProtKB/Swiss-Prot),   Q5HYC0 (UniProtKB/Swiss-Prot),   Q2TBF5 (UniProtKB/Swiss-Prot),   C9JWJ7 (UniProtKB/Swiss-Prot),   C9JSM8 (UniProtKB/Swiss-Prot),   C9JI52 (UniProtKB/Swiss-Prot),   C9JDN5 (UniProtKB/Swiss-Prot),   Q9NXN9 (UniProtKB/Swiss-Prot),   Q96L93 (UniProtKB/Swiss-Prot),   A0A140VK74 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001186794   ⟸   NM_001199865
- Peptide Label: isoform 3
- UniProtKB: A0A1B0GTU3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001186795   ⟸   NM_001199866
- Peptide Label: isoform 1
- UniProtKB: Q96L93 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005260812   ⟸   XM_005260755
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_005260811   ⟸   XM_005260754
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_005260810   ⟸   XM_005260753
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_005260808   ⟸   XM_005260751
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_005260807   ⟸   XM_005260750
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_006723651   ⟸   XM_006723588
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_016883415   ⟸   XM_017027926
- Peptide Label: isoform X9
- UniProtKB: Q96L93 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000396264   ⟸   ENST00000450176
RefSeq Acc Id: ENSP00000490639   ⟸   ENST00000635823
RefSeq Acc Id: ENSP00000489838   ⟸   ENST00000636835
RefSeq Acc Id: ENSP00000347076   ⟸   ENST00000354981
RefSeq Acc Id: ENSP00000384164   ⟸   ENST00000408042
RefSeq Acc Id: ENSP00000347995   ⟸   ENST00000355755
RefSeq Acc Id: XP_047296222   ⟸   XM_047440266
- Peptide Label: isoform X13
RefSeq Acc Id: XP_047296220   ⟸   XM_047440264
- Peptide Label: isoform X11
RefSeq Acc Id: XP_047296218   ⟸   XM_047440262
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047296221   ⟸   XM_047440265
- Peptide Label: isoform X12
RefSeq Acc Id: XP_047296219   ⟸   XM_047440263
- Peptide Label: isoform X10
RefSeq Acc Id: XP_047296217   ⟸   XM_047440261
- Peptide Label: isoform X3
RefSeq Acc Id: NP_001397782   ⟸   NM_001410853
- Peptide Label: isoform 4
- UniProtKB: A0A1B0GVS8 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054179621   ⟸   XM_054323646
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054179619   ⟸   XM_054323644
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054179617   ⟸   XM_054323642
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054179614   ⟸   XM_054323639
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054179620   ⟸   XM_054323645
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054179618   ⟸   XM_054323643
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054179616   ⟸   XM_054323641
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054179615   ⟸   XM_054323640
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054179613   ⟸   XM_054323638
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054179612   ⟸   XM_054323637
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054179611   ⟸   XM_054323636
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054179610   ⟸   XM_054323635
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054179609   ⟸   XM_054323634
- Peptide Label: isoform X1
Protein Domains
FHA   Kinesin motor   PX

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96L93-F1-model_v2 AlphaFold Q96L93 1-1317 view protein structure

Promoters
RGD ID:6798668
Promoter ID:HG_KWN:38671
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000355755,   ENST00000377997,   ENST00000378003,   ENST00000408042,   NM_024704,   UC010GCH.1,   UC010GCJ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362016,501,916 - 16,502,416 (-)MPROMDB
RGD ID:13206411
Promoter ID:EPDNEW_H26786
Type:initiation region
Name:KIF16B_1
Description:kinesin family member 16B
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
GRCh382016,573,448 - 16,573,508EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:15869 AgrOrtholog
COSMIC KIF16B COSMIC
Ensembl Genes ENSG00000089177 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000354981 ENTREZGENE
  ENST00000354981.7 UniProtKB/Swiss-Prot
  ENST00000408042 ENTREZGENE
  ENST00000408042.5 UniProtKB/Swiss-Prot
  ENST00000450176.1 UniProtKB/TrEMBL
  ENST00000635823 ENTREZGENE
  ENST00000635823.2 UniProtKB/TrEMBL
  ENST00000636835 ENTREZGENE
  ENST00000636835.1 UniProtKB/TrEMBL
Gene3D-CATH 2.60.200.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.1520.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.40.850.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000089177 GTEx
HGNC ID HGNC:15869 ENTREZGENE
Human Proteome Map KIF16B Human Proteome Map
InterPro FHA_dom 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
  Phox UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PX_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SMAD_FHA_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:55614 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 55614 ENTREZGENE
OMIM 618171 OMIM
PANTHER KINESIN-LIKE PROTEIN KIF1C ISOFORM X1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  STAR-RELATED LIPID TRANSFER PROTEIN 9 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam FHA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Kinesin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PF00787 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162393227 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
  PS50195 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART KISc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00312 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF49879 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF64268 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A140VK74 ENTREZGENE, UniProtKB/TrEMBL
  A0A1B0GTU3 ENTREZGENE, UniProtKB/TrEMBL
  A0A1B0GVS8 ENTREZGENE, UniProtKB/TrEMBL
  A6NKJ9 ENTREZGENE
  A7E2A8 ENTREZGENE
  B1AKG3 ENTREZGENE
  B1AKT7 ENTREZGENE
  C9JDN5 ENTREZGENE
  C9JI52 ENTREZGENE
  C9JSM8 ENTREZGENE
  C9JWJ7 ENTREZGENE
  H0Y534_HUMAN UniProtKB/TrEMBL
  KI16B_HUMAN UniProtKB/Swiss-Prot
  Q2TBF5 ENTREZGENE
  Q5HYC0 ENTREZGENE
  Q5HYK1 ENTREZGENE
  Q5JWW3 ENTREZGENE
  Q5TFK5 ENTREZGENE
  Q86VL9 ENTREZGENE
  Q86YS5 ENTREZGENE
  Q8IYU0 ENTREZGENE
  Q96L93 ENTREZGENE
  Q9BQJ8 ENTREZGENE
  Q9BQM0 ENTREZGENE
  Q9BQM1 ENTREZGENE
  Q9BQM5 ENTREZGENE
  Q9H5U0 ENTREZGENE
  Q9HCI2 ENTREZGENE
  Q9NXN9 ENTREZGENE
UniProt Secondary A6NKJ9 UniProtKB/Swiss-Prot
  A7E2A8 UniProtKB/Swiss-Prot
  B1AKG3 UniProtKB/Swiss-Prot
  B1AKT7 UniProtKB/Swiss-Prot
  C9JDN5 UniProtKB/Swiss-Prot
  C9JI52 UniProtKB/Swiss-Prot
  C9JSM8 UniProtKB/Swiss-Prot
  C9JWJ7 UniProtKB/Swiss-Prot
  Q2TBF5 UniProtKB/Swiss-Prot
  Q5HYC0 UniProtKB/Swiss-Prot
  Q5HYK1 UniProtKB/Swiss-Prot
  Q5JWW3 UniProtKB/Swiss-Prot
  Q5TFK5 UniProtKB/Swiss-Prot
  Q86VL9 UniProtKB/Swiss-Prot
  Q86YS5 UniProtKB/Swiss-Prot
  Q8IYU0 UniProtKB/Swiss-Prot
  Q9BQJ8 UniProtKB/Swiss-Prot
  Q9BQM0 UniProtKB/Swiss-Prot
  Q9BQM1 UniProtKB/Swiss-Prot
  Q9BQM5 UniProtKB/Swiss-Prot
  Q9H5U0 UniProtKB/Swiss-Prot
  Q9HCI2 UniProtKB/Swiss-Prot
  Q9NXN9 UniProtKB/Swiss-Prot