CLEC16A (C-type lectin domain containing 16A) - Rat Genome Database

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Gene: CLEC16A (C-type lectin domain containing 16A) Homo sapiens
Analyze
Symbol: CLEC16A
Name: C-type lectin domain containing 16A
RGD ID: 1604037
HGNC Page HGNC:29013
Description: Involved in several processes, including mitophagy; negative regulation of autophagosome maturation; and positive regulation of TORC1 signaling. Located in Golgi apparatus; cytosol; and vesicle. Implicated in Addison's disease; multiple sclerosis; rheumatoid arthritis; and type 1 diabetes mellitus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: C-type lectin domain family 16 member A; C-type lectin domain family 16, member A; Gop-1; KIAA0350; MGC111457
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
GRCh381610,944,564 - 11,182,186 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1610,944,539 - 11,182,186 (+)EnsemblGRCh38hg38GRCh38
GRCh371611,038,421 - 11,276,043 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361610,945,943 - 11,183,539 (+)NCBINCBI36Build 36hg18NCBI36
Celera1611,207,780 - 11,445,485 (+)NCBICelera
Cytogenetic Map16p13.13NCBI
HuRef1610,955,943 - 11,193,891 (+)NCBIHuRef
CHM1_11611,038,266 - 11,275,979 (+)NCBICHM1_1
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model



  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CLEC16AHumanAddison's disease  IAGP 5491177DNA:polymorphism:intron:rs12917716CRGD 
CLEC16AHumanmultiple sclerosis  IAGP 5491175DNA:polymorphism:intron:g.194570G>A and rs7184083RGD 
CLEC16AHumanrheumatoid arthritis  IAGP 5491176DNA:polymorphism:intron:rs6498169GRGD 
CLEC16AHumantype 1 diabetes mellitus  IAGP 5491176DNA:polymorphism:intron:rs2903692ARGD 
CLEC16AHumantype 1 diabetes mellitus  IAGP 2313978DNA:polymorphism:intron:rs725613 (human)RGD 
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CLEC16AHumanCharcot-Marie-Tooth disease type 1C  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1CClinVarPMID:28492532
CLEC16AHumanLandau-Kleffner syndrome  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Landau-Kleffner syndromeClinVarPMID:28492532
CLEC16AHumanMeniere's disease  IAGP (Homo sapiens) more ...8554872ClinVar Annotator: match by term: Meniere diseaseClinVar 
CLEC16AHumanMHC class II deficiency  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: MHC class II deficiencyClinVarPMID:26271388 more ...
CLEC16AHumanMHC class II deficiency  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: MHC class II deficiencyClinVarPMID:28492532
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CLEC16AHumanAddison's disease  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:18593762
CLEC16AHumanimmunoglobulin alpha deficiency  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:20694011 and PMID:27723758
CLEC16AHumanmultiple sclerosis  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:18946483 and PMID:19525955
CLEC16AHumanprimary biliary cholangitis  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:21399635
CLEC16AHumansystemic lupus erythematosus  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:19838195
CLEC16AHumantype 1 diabetes mellitus  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:17632545 and PMID:18946483
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CLEC16AHumanneurodegenerative disease  ISSClec16a (Mus musculus)13592920 MouseDO 

1 to 20 of 53 rows

  
Object Symbol
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Reference
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Original Reference(s)
CLEC16AHuman17beta-estradiol increases expressionISOClec16a (Mus musculus)6480464Estradiol results in increased expression of CLEC16A mRNACTDPMID:39298647
CLEC16AHuman2,3,7,8-tetrachlorodibenzodioxine affects expressionISOClec16a (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of CLEC16A mRNACTDPMID:21570461
CLEC16AHuman2,3,7,8-Tetrachlorodibenzofuran decreases expressionISOClec16a (Rattus norvegicus)64804642 more ...CTDPMID:32109520
CLEC16AHuman2-methylcholine affects expressionEXP 6480464beta-methylcholine affects the expression of CLEC16A mRNACTDPMID:21179406
CLEC16AHuman3,4-methylenedioxymethamphetamine decreases expressionISOClec16a (Mus musculus)6480464N-Methyl-3 and 4-methylenedioxyamphetamine results in decreased expression of CLEC16A mRNACTDPMID:26251327
CLEC16AHuman4,4'-sulfonyldiphenol decreases expressionISOClec16a (Mus musculus)6480464bisphenol S results in decreased expression of CLEC16A mRNACTDPMID:39298647
CLEC16AHumanaflatoxin B1 decreases expressionEXP 6480464Aflatoxin B1 results in decreased expression of CLEC16A mRNACTDPMID:22100608
CLEC16AHumanaflatoxin B1 increases methylationEXP 6480464Aflatoxin B1 results in increased methylation of CLEC16A intronCTDPMID:30157460
CLEC16AHumanAflatoxin B2 alpha increases methylationEXP 6480464aflatoxin B2 results in increased methylation of CLEC16A intronCTDPMID:30157460
CLEC16AHumanarsane affects methylationEXP 6480464Arsenic affects the methylation of CLEC16A geneCTDPMID:25304211
CLEC16AHumanarsenic atom affects methylationEXP 6480464Arsenic affects the methylation of CLEC16A geneCTDPMID:25304211
CLEC16AHumanatrazine decreases expressionEXP 6480464Atrazine results in decreased expression of CLEC16A mRNACTDPMID:22378314
CLEC16AHumanbenzo[a]pyrene decreases expressionEXP 6480464Benzo(a)pyrene results in decreased expression of CLEC16A mRNACTDPMID:20064835 more ...
CLEC16AHumanbenzo[a]pyrene decreases methylationEXP 6480464Benzo(a)pyrene results in decreased methylation of CLEC16A 3' UTRCTDPMID:27901495
CLEC16AHumanbenzo[a]pyrene affects methylationEXP 6480464Benzo(a)pyrene affects the methylation of CLEC16A intron and Benzo(a)pyrene affects the methylation of CLEC16A promoterCTDPMID:27901495 and PMID:30157460
CLEC16AHumanbenzo[a]pyrene diol epoxide I decreases expressionEXP 64804647 more ...CTDPMID:26238291
CLEC16AHumanbisphenol A decreases expressionISOClec16a (Rattus norvegicus)6480464bisphenol A results in decreased expression of CLEC16A mRNACTDPMID:25181051 more ...
CLEC16AHumanbisphenol A decreases methylationEXP 6480464bisphenol A results in decreased methylation of CLEC16A geneCTDPMID:31601247
CLEC16AHumanbisphenol A multiple interactionsEXP 6480464[bisphenol A co-treated with Fulvestrant] results in decreased methylation of CLEC16A geneCTDPMID:31601247
CLEC16AHumancadmium dichloride decreases expressionEXP 6480464Cadmium Chloride results in decreased expression of CLEC16A mRNACTDPMID:38568856

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Biological Process
1 to 14 of 14 rows

  
Object Symbol
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Source
Original Reference(s)
CLEC16AHumanautophagy involved_inIEAUniProtKB-KW:KW-0072150520179 UniProtGO_REF:0000043
CLEC16AHumancellular response to starvation involved_inIMP 150520179 PMID:28223137UniProtPMID:28223137
CLEC16AHumanendosomal transport involved_inIBAFB:FBgn0038427 and PANTHER:PTN000486192150520179 GO_CentralGO_REF:0000033
CLEC16AHumanmitophagy involved_inIDA 150520179 PMID:35604110DisProtPMID:35604110
CLEC16AHumannegative regulation of autophagosome maturation involved_inIMP 150520179 PMID:28223137UniProtPMID:28223137
CLEC16AHumannegative regulation of mitophagy acts_upstream_of_or_withinISOMGI:56486339068941 PMID:24949970MGIPMID:24949970
CLEC16AHumannegative regulation of proteasomal ubiquitin-dependent protein catabolic process acts_upstream_of_or_withinISOMGI:56486339068941 PMID:24949970MGIPMID:24949970
CLEC16AHumanpositive regulation of autophagosome maturation acts_upstream_of_or_withinISOMGI:56486339068941 PMID:24949970MGIPMID:24949970
CLEC16AHumanpositive regulation of TORC1 signaling involved_inIMP 150520179 PMID:28223137UniProtPMID:28223137
CLEC16AHumanproteasome-mediated ubiquitin-dependent protein catabolic process acts_upstream_ofISOMGI:56486339068941 PMID:24949970MGIPMID:24949970
CLEC16AHumanprotein destabilization involved_inISOClec16a (Mus musculus)9068941 PMID:36822331DisProtPMID:36822331
CLEC16AHumanregulation of autophagosome maturation involved_inIBAMGI:1921624 more ...150520179 GO_CentralGO_REF:0000033
CLEC16AHumanregulation of proteasomal ubiquitin-dependent protein catabolic process involved_inISOUniProtKB:Q8BH759068941 PMID:36822331DisProtPMID:36822331
CLEC16AHumanvacuolar transport involved_inIBAFB:FBgn0038427 and PANTHER:PTN000486192150520179 GO_CentralGO_REF:0000033
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Cellular Component
1 to 11 of 11 rows

  
Object Symbol
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Original Reference(s)
CLEC16AHumancytosol located_inIDA 150520179 PMID:28223137UniProtPMID:28223137
CLEC16AHumanendolysosome membrane located_inISOClec16a (Mus musculus)9068941 PMID:24949970MGIPMID:24949970
CLEC16AHumanendosome located_inIEAUniProtKB-KW:KW-0967150520179 UniProtGO_REF:0000043
CLEC16AHumanendosome membrane located_inIEAUniProtKB-SubCell:SL-0100150520179 UniProtGO_REF:0000044
CLEC16AHumanGolgi apparatus located_inIDA 150520179 PMID:28223137UniProtPMID:28223137
CLEC16AHumanGolgi apparatus is_active_inIBAFB:FBgn0038427 more ...150520179 GO_CentralGO_REF:0000033
CLEC16AHumanlate endosome located_inIBAFB:FBgn0038427 and PANTHER:PTN000486192150520179 GO_CentralGO_REF:0000033
CLEC16AHumanlysosomal membrane located_inIEAUniProtKB-SubCell:SL-0157150520179 UniProtGO_REF:0000044
CLEC16AHumanlysosome located_inIEAUniProtKB-KW:KW-0458150520179 UniProtGO_REF:0000043
CLEC16AHumanmembrane located_inIEAUniProtKB-KW:KW-0472150520179 UniProtGO_REF:0000043
CLEC16AHumanvesicle located_inIDA 150520179 PMID:28223137UniProtPMID:28223137
1 to 11 of 11 rows

Molecular Function

  
Object Symbol
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Term
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Reference
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Original Reference(s)
CLEC16AHumanprotein binding enablesIPIUniProtKB:P14373150520179 PMID:36538041IntActPMID:36538041


#
Reference Title
Reference Citation
1. Chromosomal region 16p13: further evidence of increased predisposition to immune diseases. Martinez A, etal., Ann Rheum Dis. 2010 Jan;69(1):309-11. Epub .
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
3. Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency. Skinningsrud B, etal., J Clin Endocrinol Metab. 2008 Sep;93(9):3310-7. Epub 2008 Jul 1.
4. Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia. Zoledziewska M, etal., Genes Immun. 2009 Jan;10(1):15-7. Epub 2008 Oct 23.
5. Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex. Zuvich RL, etal., Hum Mol Genet. 2011 Sep 1;20(17):3517-24. Epub 2011 Jun 8.
PMID:9205841   PMID:12168954   PMID:12477932   PMID:14702039   PMID:15489334   PMID:16344560   PMID:17554260   PMID:17554300   PMID:17632545   PMID:17660530   PMID:18650830   PMID:18940880  
PMID:18978792   PMID:18987646   PMID:19073967   PMID:19178520   PMID:19264985   PMID:19305408   PMID:19317741   PMID:19337309   PMID:19375175   PMID:19430480   PMID:19506219   PMID:19525953  
PMID:19525955   PMID:19734133   PMID:19834503   PMID:19838195   PMID:19851296   PMID:19865102   PMID:19879194   PMID:19951419   PMID:20036365   PMID:20043139   PMID:20095854   PMID:20190752  
PMID:20198315   PMID:20203524   PMID:20220768   PMID:20368992   PMID:20372818   PMID:20379614   PMID:20450971   PMID:20694011   PMID:20805369   PMID:20849399   PMID:20962850   PMID:21179112  
PMID:21399635   PMID:21829393   PMID:21833088   PMID:21873635   PMID:22036096   PMID:22257840   PMID:22534877   PMID:23042114   PMID:23133532   PMID:23151489   PMID:23251661   PMID:23273568  
PMID:23817569   PMID:24388013   PMID:24646814   PMID:24949970   PMID:25008175   PMID:25447402   PMID:25576669   PMID:25823473   PMID:25891430   PMID:25903733   PMID:26121298   PMID:26186194  
PMID:26203907   PMID:26472760   PMID:26496610   PMID:26987296   PMID:28223137   PMID:28514442   PMID:28581483   PMID:28611215   PMID:28617357   PMID:28718761   PMID:28986522   PMID:29180353  
PMID:29507755   PMID:30774629   PMID:30970177   PMID:32641384   PMID:33232298   PMID:33961781   PMID:34079125   PMID:34643957   PMID:35013429   PMID:35271311   PMID:35509820   PMID:35604110  
PMID:35844135   PMID:36538041   PMID:36622793   PMID:37175930   PMID:37827155   PMID:38569033   PMID:38777146  



CLEC16A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381610,944,564 - 11,182,186 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1610,944,539 - 11,182,186 (+)EnsemblGRCh38hg38GRCh38
GRCh371611,038,421 - 11,276,043 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361610,945,943 - 11,183,539 (+)NCBINCBI36Build 36hg18NCBI36
Celera1611,207,780 - 11,445,485 (+)NCBICelera
Cytogenetic Map16p13.13NCBI
HuRef1610,955,943 - 11,193,891 (+)NCBIHuRef
CHM1_11611,038,266 - 11,275,979 (+)NCBICHM1_1
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBIT2T-CHM13v2.0
Clec16a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391610,363,173 - 10,562,742 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1610,363,203 - 10,562,742 (+)EnsemblGRCm39 Ensembl
GRCm381610,545,309 - 10,744,878 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1610,545,339 - 10,744,878 (+)EnsemblGRCm38mm10GRCm38
MGSCv371610,545,480 - 10,744,964 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361610,458,965 - 10,658,449 (+)NCBIMGSCv36mm8
Celera1611,178,067 - 11,375,698 (+)NCBICelera
Cytogenetic Map16A1NCBI
cM Map165.68NCBI
Clec16a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8105,434,725 - 5,631,246 (-)NCBIGRCr8
mRatBN7.2104,927,799 - 5,123,749 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl104,928,030 - 5,123,578 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx109,624,383 - 9,820,126 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0109,145,490 - 9,341,240 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0104,783,769 - 4,979,511 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0105,002,196 - 5,196,914 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl105,009,826 - 5,196,892 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0103,827,156 - 4,020,226 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4104,870,719 - 5,069,691 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1104,873,502 - 5,072,213 (-)NCBI
Celera103,948,821 - 4,141,759 (-)NCBICelera
Cytogenetic Map10q11NCBI
Clec16a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554427,368,952 - 7,584,703 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554427,369,616 - 7,584,052 (-)NCBIChiLan1.0ChiLan1.0
CLEC16A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21811,495,055 - 11,731,694 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11615,270,314 - 15,506,950 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0169,887,877 - 10,124,500 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11611,109,639 - 11,346,971 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1611,109,869 - 11,343,512 (+)Ensemblpanpan1.1panPan2
CLEC16A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1631,560,940 - 31,757,100 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl631,562,834 - 31,757,678 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha632,943,444 - 33,139,557 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0631,743,163 - 31,939,531 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl631,743,173 - 31,939,523 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1631,556,477 - 31,752,772 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0631,430,738 - 31,627,044 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0631,855,194 - 32,051,540 (-)NCBIUU_Cfam_GSD_1.0
Clec16a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344111,244,073 - 111,419,122 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365309,089,476 - 9,264,592 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365309,089,478 - 9,264,563 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CLEC16A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl331,938,135 - 32,158,320 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1331,938,133 - 32,158,343 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2332,799,756 - 32,868,904 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CLEC16A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1510,420,866 - 10,658,370 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl510,420,931 - 10,658,507 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366606819,506,544 - 19,745,864 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Clec16a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248248,174,610 - 8,400,723 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248248,174,653 - 8,400,760 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in CLEC16A
164 total Variants

1 to 10 of 152 rows
Name
Type
Condition(s)
Position(s)
Clinical significance
GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3 copy number gain See cases [RCV000052367] Chr16:23141..11296695 [GRCh38]
Chr16:73141..11390552 [GRCh37]
Chr16:13141..11298053 [NCBI36]
Chr16:16p13.3-13.13
pathogenic
GRCh38/hg38 16p13.3-11.2(chr16:4644892-29170820)x3 copy number gain See cases [RCV000133809] Chr16:4644892..29170820 [GRCh38]
Chr16:4694893..29182141 [GRCh37]
Chr16:4634894..29089642 [NCBI36]
Chr16:16p13.3-11.2
pathogenic
GRCh38/hg38 16p13.3-13.13(chr16:46766-11525516)x3 copy number gain See cases [RCV000133780] Chr16:46766..11525516 [GRCh38]
Chr16:96766..11619372 [GRCh37]
Chr16:36766..11526873 [NCBI36]
Chr16:16p13.3-13.13
pathogenic
GRCh38/hg38 16p13.13(chr16:10778551-11374173)x3 copy number gain See cases [RCV000137607] Chr16:10778551..11374173 [GRCh38]
Chr16:10872408..11468030 [GRCh37]
Chr16:10779909..11375531 [NCBI36]
Chr16:16p13.13
likely benign
GRCh38/hg38 16p13.3-13.12(chr16:43732-13326806)x3 copy number gain See cases [RCV000139166] Chr16:43732..13326806 [GRCh38]
Chr16:93732..13420663 [GRCh37]
Chr16:33732..13328164 [NCBI36]
Chr16:16p13.3-13.12
pathogenic
GRCh37/hg19 16p13.13(chr16:11173868-11681288)x3 copy number gain See cases [RCV000240209] Chr16:11173868..11681288 [GRCh37]
Chr16:16p13.13
uncertain significance
GRCh38/hg38 16p13.3-13.11(chr16:666662-15743104)x3 copy number gain See cases [RCV000143710] Chr16:666662..15743104 [GRCh38]
Chr16:716662..15836961 [GRCh37]
Chr16:656663..15744462 [NCBI36]
Chr16:16p13.3-13.11
pathogenic
GRCh37/hg19 16p13.3-11.2(chr16:102839-28327676)x3 copy number gain See cases [RCV000203445] Chr16:102839..28327676 [GRCh37]
Chr16:16p13.3-11.2
pathogenic
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3 copy number gain Breast ductal adenocarcinoma [RCV000207053] Chr16:1279324..31926800 [GRCh37]
Chr16:16p13.3-11.2
uncertain significance
GRCh37/hg19 16p13.3-12.3(chr16:1274615-19073133)x3 copy number gain Breast ductal adenocarcinoma [RCV000207326] Chr16:1274615..19073133 [GRCh37]
Chr16:16p13.3-12.3
uncertain significance
1 to 10 of 152 rows

Predicted Target Of
Summary Value
Count of predictions:9783
Count of miRNA genes:1217
Interacting mature miRNAs:1537
Transcripts:ENST00000261657, ENST00000381822, ENST00000409552, ENST00000409790, ENST00000428742, ENST00000436973, ENST00000459723, ENST00000463459, ENST00000463896, ENST00000465491, ENST00000476025, ENST00000487189, ENST00000494853
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.


1 to 10 of 182 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
407128901GWAS777877_Hmultiple sclerosis QTL GWAS777877 (human)0.0000002multiple sclerosis161107283111072832Human
597052052GWAS1148126_Hmultiple sclerosis QTL GWAS1148126 (human)4e-09multiple sclerosis161102065511020656Human
406989377GWAS638353_Hmultiple sclerosis QTL GWAS638353 (human)1e-09multiple sclerosis161114127311141274Human
406909252GWAS558228_Hsystemic lupus erythematosus QTL GWAS558228 (human)0.0000005systemic lupus erythematosus161109603111096032Human
597300637GWAS1396711_Hprimary biliary cirrhosis QTL GWAS1396711 (human)0.000002primary biliary cirrhosis161109539911095400Human
597064862GWAS1160936_Halopecia areata QTL GWAS1160936 (human)0.0000002alopecia areata161110022311100224Human
597236885GWAS1332959_HBMI-adjusted waist-hip ratio QTL GWAS1332959 (human)3e-09body size trait (VT:0100005)161106033311060334Human
597282964GWAS1379038_Heosinophil count QTL GWAS1379038 (human)6e-76eosinophil quantity (VT:0002602)blood eosinophil count (CMO:0000033)161107168511071686Human
407336777GWAS985753_Heosinophil count QTL GWAS985753 (human)6e-13eosinophil quantity (VT:0002602)blood eosinophil count (CMO:0000033)161106707211067073Human
597212822GWAS1308896_Htype 2 diabetes mellitus QTL GWAS1308896 (human)2e-16type 2 diabetes mellitus161110694111106942Human

1 to 10 of 182 rows
D16S3122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,214,644 - 11,214,770UniSTSGRCh37
Build 361611,122,145 - 11,122,271RGDNCBI36
Celera1611,384,091 - 11,384,215RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,132,494 - 11,132,618UniSTS
Marshfield Genetic Map1620.77RGD
Marshfield Genetic Map1620.77UniSTS
Genethon Genetic Map1619.7UniSTS
deCODE Assembly Map1628.3UniSTS
Whitehead-YAC Contig Map16 UniSTS
D16S414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,052,781 - 11,052,945UniSTSGRCh37
GRCh371611,052,830 - 11,052,984UniSTSGRCh37
Build 361610,960,331 - 10,960,485RGDNCBI36
Celera1611,222,218 - 11,222,380UniSTS
Celera1611,222,267 - 11,222,419RGD
Cytogenetic Map16p13.13UniSTS
HuRef1610,970,382 - 10,970,546UniSTS
HuRef1610,970,431 - 10,970,585UniSTS
Marshfield Genetic Map1620.77UniSTS
Marshfield Genetic Map1620.77RGD
Genethon Genetic Map1619.7UniSTS
TNG Radiation Hybrid Map165418.0UniSTS
Stanford-G3 RH Map16504.0UniSTS
GeneMap99-GB4 RH Map16105.93UniSTS
Whitehead-RH Map1653.7UniSTS
Whitehead-YAC Contig Map16 UniSTS
NCBI RH Map16115.1UniSTS
GeneMap99-G3 RH Map16464.0UniSTS
D16S497  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,080,468 - 11,080,679UniSTSGRCh37
GRCh371611,080,517 - 11,080,678UniSTSGRCh37
Build 361610,988,018 - 10,988,179RGDNCBI36
Celera1611,249,903 - 11,250,114UniSTS
Celera1611,249,952 - 11,250,113RGD
Cytogenetic Map16p13.3-p12.1UniSTS
Cytogenetic Map16p13.13UniSTS
HuRef1610,997,975 - 10,998,186UniSTS
HuRef1610,998,024 - 10,998,185UniSTS
Marshfield Genetic Map1620.77UniSTS
Marshfield Genetic Map1620.77RGD
Genethon Genetic Map1619.7UniSTS
TNG Radiation Hybrid Map165443.0UniSTS
Stanford-G3 RH Map16509.0UniSTS
GeneMap99-GB4 RH Map16108.36UniSTS
Whitehead-RH Map1651.7UniSTS
Whitehead-YAC Contig Map16 UniSTS
NCBI RH Map16113.0UniSTS
GeneMap99-G3 RH Map16469.0UniSTS
SHGC-60718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,220,029 - 11,220,168UniSTSGRCh37
Build 361611,127,530 - 11,127,669RGDNCBI36
Celera1611,389,473 - 11,389,612RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,137,877 - 11,138,016UniSTS
GeneMap99-GB4 RH Map16113.47UniSTS
Whitehead-RH Map1653.8UniSTS
NCBI RH Map16139.9UniSTS
SHGC-32917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,250,954 - 11,251,063UniSTSGRCh37
Build 361611,158,455 - 11,158,564RGDNCBI36
Celera1611,420,397 - 11,420,506RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,168,803 - 11,168,912UniSTS
TNG Radiation Hybrid Map165537.0UniSTS
Stanford-G3 RH Map16519.0UniSTS
GeneMap99-GB4 RH Map16101.01UniSTS
Whitehead-RH Map1656.6UniSTS
NCBI RH Map16120.3UniSTS
GeneMap99-G3 RH Map16479.0UniSTS
RH47514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,250,913 - 11,251,063UniSTSGRCh37
Build 361611,158,414 - 11,158,564RGDNCBI36
Celera1611,420,356 - 11,420,506RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,168,762 - 11,168,912UniSTS
GeneMap99-GB4 RH Map16114.25UniSTS
RH8139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,111,611 - 11,111,770UniSTSGRCh37
Build 361611,019,112 - 11,019,271RGDNCBI36
Celera1611,281,046 - 11,281,205RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,029,116 - 11,029,275UniSTS
SHGC-82550  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,170,518 - 11,170,844UniSTSGRCh37
Build 361611,078,019 - 11,078,345RGDNCBI36
Celera1611,339,960 - 11,340,286RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,088,337 - 11,088,663UniSTS
TNG Radiation Hybrid Map165486.0UniSTS
SHGC-152679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,052,811 - 11,053,022UniSTSGRCh37
Build 361610,960,312 - 10,960,523RGDNCBI36
Celera1611,222,248 - 11,222,457RGD
Cytogenetic Map16p13.13UniSTS
HuRef1610,970,412 - 10,970,623UniSTS
TNG Radiation Hybrid Map124155.0UniSTS
D16S3335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,275,863 - 11,276,000UniSTSGRCh37
Build 361611,183,364 - 11,183,501RGDNCBI36
Celera1611,445,302 - 11,445,439RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,193,708 - 11,193,845UniSTS
D16S3285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,197,792 - 11,197,974UniSTSGRCh37
Build 361611,105,293 - 11,105,475RGDNCBI36
Celera1611,367,243 - 11,367,425RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,115,626 - 11,115,808UniSTS
Stanford-G3 RH Map16514.0UniSTS
SHGC-2756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,197,472 - 11,197,615UniSTSGRCh37
Build 361611,104,973 - 11,105,116RGDNCBI36
Celera1611,366,923 - 11,367,066RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,115,306 - 11,115,449UniSTS
TNG Radiation Hybrid Map165529.0UniSTS
SHGC-61091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,275,802 - 11,276,018UniSTSGRCh37
Build 361611,183,303 - 11,183,519RGDNCBI36
Celera1611,445,241 - 11,445,457RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,193,647 - 11,193,863UniSTS
GeneMap99-GB4 RH Map1699.02UniSTS
SHGC-60777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,220,490 - 11,220,639UniSTSGRCh37
Build 361611,127,991 - 11,128,140RGDNCBI36
Celera1611,389,934 - 11,390,083RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,138,338 - 11,138,487UniSTS
GeneMap99-GB4 RH Map1698.84UniSTS
Whitehead-RH Map1659.4UniSTS
NCBI RH Map16123.4UniSTS
RH70169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,224,687 - 11,224,811UniSTSGRCh37
Build 361611,132,188 - 11,132,312RGDNCBI36
Celera1611,394,131 - 11,394,255RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,142,535 - 11,142,659UniSTS
GeneMap99-GB4 RH Map1698.81UniSTS
SHGC-60572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371611,224,696 - 11,224,845UniSTSGRCh37
Build 361611,132,197 - 11,132,346RGDNCBI36
Celera1611,394,140 - 11,394,289RGD
Cytogenetic Map16p13.13UniSTS
HuRef1611,142,544 - 11,142,693UniSTS
GeneMap99-GB4 RH Map1698.81UniSTS
Whitehead-RH Map1657.5UniSTS
NCBI RH Map16122.4UniSTS
D16S414  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16p13.13UniSTS
NCBI RH Map16113.0UniSTS
D16S497  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16p13.13UniSTS
TNG Radiation Hybrid Map165443.0UniSTS
Stanford-G3 RH Map16509.0UniSTS
GeneMap99-G3 RH Map16469.0UniSTS




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
renal system
reproductive system
respiratory system
sensory system
1204 2434 2788 2246 4954 1723 2346 6 622 1949 464 2268 7285 6456 52 3720 848 1733 1613 171


1 to 30 of 94 rows
RefSeq Transcripts NG_016757 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001243403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001410905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_015226 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005255211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005255213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005255214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005255215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005255216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006720870 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011522434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011522435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011522436 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011522437 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011522438 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011522439 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011522440 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433848 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433850 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433851 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433853 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433854 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433855 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433856 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 30 of 94 rows

Ensembl Acc Id: ENST00000261657   ⟹   ENSP00000261657
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,123,900 - 11,182,181 (+)Ensembl
Ensembl Acc Id: ENST00000409552   ⟹   ENSP00000386495
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1610,944,581 - 11,126,787 (+)Ensembl
Ensembl Acc Id: ENST00000409790   ⟹   ENSP00000387122
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1610,944,564 - 11,182,186 (+)Ensembl
Ensembl Acc Id: ENST00000428742   ⟹   ENSP00000389743
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,123,743 - 11,157,225 (+)Ensembl
Ensembl Acc Id: ENST00000436973   ⟹   ENSP00000389963
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,123,895 - 11,157,233 (+)Ensembl
Ensembl Acc Id: ENST00000459723   ⟹   ENSP00000493756
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,126,010 - 11,150,317 (+)Ensembl
Ensembl Acc Id: ENST00000463459
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,024,867 - 11,048,512 (+)Ensembl
Ensembl Acc Id: ENST00000463896
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,024,153 - 11,048,518 (+)Ensembl
Ensembl Acc Id: ENST00000465491
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,024,480 - 11,123,920 (+)Ensembl
Ensembl Acc Id: ENST00000476025
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,024,473 - 11,047,342 (+)Ensembl
Ensembl Acc Id: ENST00000487189
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,024,818 - 11,044,222 (+)Ensembl
Ensembl Acc Id: ENST00000494853
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1610,972,481 - 11,024,919 (+)Ensembl
Ensembl Acc Id: ENST00000646363
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1611,024,508 - 11,136,283 (+)Ensembl
Ensembl Acc Id: ENST00000703130   ⟹   ENSP00000515187
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1610,944,539 - 11,182,182 (+)Ensembl
RefSeq Acc Id: NM_001243403   ⟹   NP_001230332
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,126,344 (+)NCBI
GRCh371611,038,345 - 11,276,046 (+)NCBI
HuRef1610,955,943 - 11,193,891 (+)NCBI
CHM1_11611,038,266 - 11,220,129 (+)NCBI
T2T-CHM13v2.01610,980,535 - 11,162,623 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001410905   ⟹   NP_001397834
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: NM_015226   ⟹   NP_056041
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
GRCh371611,038,345 - 11,276,046 (+)ENTREZGENE
Build 361610,945,943 - 11,183,539 (+)NCBI Archive
HuRef1610,955,943 - 11,193,891 (+)ENTREZGENE
CHM1_11611,038,266 - 11,275,979 (+)NCBI
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005255211   ⟹   XP_005255268
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
GRCh371611,038,345 - 11,276,046 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005255213   ⟹   XP_005255270
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
GRCh371611,038,345 - 11,276,046 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005255214   ⟹   XP_005255271
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
GRCh371611,038,345 - 11,276,046 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005255215   ⟹   XP_005255272
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,157,225 (+)NCBI
GRCh371611,038,345 - 11,276,046 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005255216   ⟹   XP_005255273
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,157,225 (+)NCBI
GRCh371611,038,345 - 11,276,046 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006720870   ⟹   XP_006720933
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,052,724 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011522434   ⟹   XP_011520736
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011522436   ⟹   XP_011520738
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,137,173 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011522437   ⟹   XP_011520739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,137,173 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011522438   ⟹   XP_011520740
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,150,314 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011522439   ⟹   XP_011520741
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,137,173 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011522440   ⟹   XP_011520742
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,137,173 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017023089   ⟹   XP_016878578
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,052,724 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017023090   ⟹   XP_016878579
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381611,036,025 - 11,182,186 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024450218   ⟹   XP_024305986
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,157,225 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024450219   ⟹   XP_024305987
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381611,024,323 - 11,182,186 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047433847   ⟹   XP_047289803
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
RefSeq Acc Id: XM_047433848   ⟹   XP_047289804
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
RefSeq Acc Id: XM_047433850   ⟹   XP_047289806
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
RefSeq Acc Id: XM_047433851   ⟹   XP_047289807
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
RefSeq Acc Id: XM_047433852   ⟹   XP_047289808
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,182,186 (+)NCBI
RefSeq Acc Id: XM_047433853   ⟹   XP_047289809
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,174,276 (+)NCBI
RefSeq Acc Id: XM_047433854   ⟹   XP_047289810
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,174,276 (+)NCBI
RefSeq Acc Id: XM_047433855   ⟹   XP_047289811
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,174,276 (+)NCBI
RefSeq Acc Id: XM_047433856   ⟹   XP_047289812
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,174,276 (+)NCBI
RefSeq Acc Id: XM_047433857   ⟹   XP_047289813
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,137,173 (+)NCBI
RefSeq Acc Id: XM_047433858   ⟹   XP_047289814
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,150,314 (+)NCBI
RefSeq Acc Id: XM_047433859   ⟹   XP_047289815
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,137,173 (+)NCBI
RefSeq Acc Id: XM_047433860   ⟹   XP_047289816
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,157,225 (+)NCBI
RefSeq Acc Id: XM_047433861   ⟹   XP_047289817
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,150,314 (+)NCBI
RefSeq Acc Id: XM_047433862   ⟹   XP_047289818
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,150,314 (+)NCBI
RefSeq Acc Id: XM_047433863   ⟹   XP_047289819
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,137,173 (+)NCBI
RefSeq Acc Id: XM_047433864   ⟹   XP_047289820
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,137,173 (+)NCBI
RefSeq Acc Id: XM_047433865   ⟹   XP_047289821
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,137,173 (+)NCBI
RefSeq Acc Id: XM_047433866   ⟹   XP_047289822
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,157,225 (+)NCBI
RefSeq Acc Id: XM_047433867   ⟹   XP_047289823
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,150,314 (+)NCBI
RefSeq Acc Id: XM_047433868   ⟹   XP_047289824
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381610,944,564 - 11,052,724 (+)NCBI
RefSeq Acc Id: XM_054379917   ⟹   XP_054235892
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379918   ⟹   XP_054235893
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379919   ⟹   XP_054235894
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379920   ⟹   XP_054235895
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379921   ⟹   XP_054235896
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379922   ⟹   XP_054235897
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379923   ⟹   XP_054235898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379924   ⟹   XP_054235899
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379925   ⟹   XP_054235900
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379926   ⟹   XP_054235901
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,210,556 (+)NCBI
RefSeq Acc Id: XM_054379927   ⟹   XP_054235902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,210,556 (+)NCBI
RefSeq Acc Id: XM_054379928   ⟹   XP_054235903
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,186,157 (+)NCBI
RefSeq Acc Id: XM_054379929   ⟹   XP_054235904
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,186,157 (+)NCBI
RefSeq Acc Id: XM_054379930   ⟹   XP_054235905
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,210,556 (+)NCBI
RefSeq Acc Id: XM_054379931   ⟹   XP_054235906
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,210,556 (+)NCBI
RefSeq Acc Id: XM_054379932   ⟹   XP_054235907
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,186,157 (+)NCBI
RefSeq Acc Id: XM_054379933   ⟹   XP_054235908
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,193,505 (+)NCBI
RefSeq Acc Id: XM_054379934   ⟹   XP_054235909
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,193,505 (+)NCBI
RefSeq Acc Id: XM_054379935   ⟹   XP_054235910
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,192,660 (+)NCBI
RefSeq Acc Id: XM_054379936   ⟹   XP_054235911
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,192,660 (+)NCBI
RefSeq Acc Id: XM_054379937   ⟹   XP_054235912
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,186,157 (+)NCBI
RefSeq Acc Id: XM_054379938   ⟹   XP_054235913
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,186,157 (+)NCBI
RefSeq Acc Id: XM_054379939   ⟹   XP_054235914
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,186,157 (+)NCBI
RefSeq Acc Id: XM_054379940   ⟹   XP_054235915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,193,505 (+)NCBI
RefSeq Acc Id: XM_054379941   ⟹   XP_054235916
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,193,505 (+)NCBI
RefSeq Acc Id: XM_054379942   ⟹   XP_054235917
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,192,660 (+)NCBI
RefSeq Acc Id: XM_054379943   ⟹   XP_054235918
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,192,660 (+)NCBI
RefSeq Acc Id: XM_054379944   ⟹   XP_054235919
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,186,157 (+)NCBI
RefSeq Acc Id: XM_054379945   ⟹   XP_054235920
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,186,157 (+)NCBI
RefSeq Acc Id: XM_054379946   ⟹   XP_054235921
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,186,157 (+)NCBI
RefSeq Acc Id: XM_054379947   ⟹   XP_054235922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,193,505 (+)NCBI
RefSeq Acc Id: XM_054379948   ⟹   XP_054235923
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,192,660 (+)NCBI
RefSeq Acc Id: XM_054379949   ⟹   XP_054235924
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,089,004 (+)NCBI
RefSeq Acc Id: XM_054379950   ⟹   XP_054235925
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,089,004 (+)NCBI
RefSeq Acc Id: XM_054379951   ⟹   XP_054235926
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01610,980,535 - 11,089,004 (+)NCBI
RefSeq Acc Id: XM_054379952   ⟹   XP_054235927
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01611,060,603 - 11,218,466 (+)NCBI
RefSeq Acc Id: XM_054379953   ⟹   XP_054235928
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01611,072,305 - 11,218,466 (+)NCBI
1 to 30 of 87 rows
Protein RefSeqs NP_001230332 (Get FASTA)   NCBI Sequence Viewer  
  NP_001397834 (Get FASTA)   NCBI Sequence Viewer  
  NP_056041 (Get FASTA)   NCBI Sequence Viewer  
  XP_005255268 (Get FASTA)   NCBI Sequence Viewer  
  XP_005255270 (Get FASTA)   NCBI Sequence Viewer  
  XP_005255271 (Get FASTA)   NCBI Sequence Viewer  
  XP_005255272 (Get FASTA)   NCBI Sequence Viewer  
  XP_005255273 (Get FASTA)   NCBI Sequence Viewer  
  XP_006720933 (Get FASTA)   NCBI Sequence Viewer  
  XP_011520736 (Get FASTA)   NCBI Sequence Viewer  
  XP_011520738 (Get FASTA)   NCBI Sequence Viewer  
  XP_011520739 (Get FASTA)   NCBI Sequence Viewer  
  XP_011520740 (Get FASTA)   NCBI Sequence Viewer  
  XP_011520741 (Get FASTA)   NCBI Sequence Viewer  
  XP_011520742 (Get FASTA)   NCBI Sequence Viewer  
  XP_016878578 (Get FASTA)   NCBI Sequence Viewer  
  XP_016878579 (Get FASTA)   NCBI Sequence Viewer  
  XP_024305986 (Get FASTA)   NCBI Sequence Viewer  
  XP_024305987 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289803 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289804 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289806 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289807 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289808 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289809 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289810 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289811 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289812 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289813 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289814 (Get FASTA)   NCBI Sequence Viewer  
1 to 30 of 87 rows
1 to 5 of 84 rows
1 to 5 of 84 rows
RefSeq Acc Id: NP_056041   ⟸   NM_015226
- Peptide Label: isoform 1
- UniProtKB: O15058 (UniProtKB/Swiss-Prot),   Q6ZTB2 (UniProtKB/Swiss-Prot),   Q2KHT3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001230332   ⟸   NM_001243403
- Peptide Label: isoform 2
- UniProtKB: Q2KHT3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005255271   ⟸   XM_005255214
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_005255268   ⟸   XM_005255211
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_005255270   ⟸   XM_005255213
- Peptide Label: isoform X2
- Sequence:
CLEC16A/TT9 C-terminal   FPL

Name Modeler Protein Id AA Range Protein Structure
AF-Q2KHT3-F1-model_v2 AlphaFold Q2KHT3 1-1053 view protein structure

RGD ID:7231323
Promoter ID:EPDNEW_H21408
Type:initiation region
Name:CLEC16A_1
Description:C-type lectin domain containing 16A
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
GRCh381610,944,564 - 10,944,624EPDNEW
RGD ID:6792917
Promoter ID:HG_KWN:23022
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000409552,   ENST00000409790,   NM_015226,   UC002DAO.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361610,945,694 - 10,946,194 (+)MPROMDB
RGD ID:6792916
Promoter ID:HG_KWN:23023
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562
Transcripts:OTTHUMT00000328544
Position:
Human AssemblyChrPosition (strand)Source
Build 361610,973,036 - 10,973,687 (+)MPROMDB


1 to 32 of 32 rows
Database
Acc Id
Source(s)
COSMIC CLEC16A COSMIC
Ensembl Genes ENSG00000038532 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000409552 ENTREZGENE
  ENST00000409552.4 UniProtKB/Swiss-Prot
  ENST00000409790 ENTREZGENE
  ENST00000409790.6 UniProtKB/Swiss-Prot
  ENST00000703130 ENTREZGENE
GTEx ENSG00000038532 GTEx
HGNC ID HGNC:29013 ENTREZGENE
Human Proteome Map CLEC16A Human Proteome Map
InterPro CLEC16A/TT9 UniProtKB/Swiss-Prot
  CLEC16A/TT9_N UniProtKB/Swiss-Prot
  CLEC16A_C UniProtKB/Swiss-Prot
KEGG Report hsa:23274 UniProtKB/Swiss-Prot
NCBI Gene 23274 ENTREZGENE
OMIM 611303 OMIM
PANTHER PROTEIN CLEC16A UniProtKB/Swiss-Prot
  PTHR21481 UniProtKB/Swiss-Prot
Pfam CLEC16A_C UniProtKB/Swiss-Prot
  FPL UniProtKB/Swiss-Prot
PharmGKB PA162382340 PharmGKB
UniProt A0A2R8YDG4_HUMAN UniProtKB/TrEMBL
  A0A8V8TR67 ENTREZGENE, UniProtKB/TrEMBL
  CL16A_HUMAN UniProtKB/Swiss-Prot
  H7BXG1_HUMAN UniProtKB/TrEMBL
  H7BZI2_HUMAN UniProtKB/TrEMBL
  H7BZJ9_HUMAN UniProtKB/TrEMBL
  O15058 ENTREZGENE
  Q2KHT3 ENTREZGENE
  Q6ZTB2 ENTREZGENE
UniProt Secondary O15058 UniProtKB/Swiss-Prot
  Q6ZTB2 UniProtKB/Swiss-Prot
1 to 32 of 32 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-03-28 CLEC16A  C-type lectin domain containing 16A  CLEC16A  C-type lectin domain family 16 member A  Symbol and/or name change 5135510 APPROVED
2015-12-22 CLEC16A  C-type lectin domain family 16 member A  CLEC16A  C-type lectin domain family 16, member A  Symbol and/or name change 5135510 APPROVED