ZBTB16 (zinc finger and BTB domain containing 16) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: ZBTB16 (zinc finger and BTB domain containing 16) Homo sapiens
Analyze
Symbol: ZBTB16
Name: zinc finger and BTB domain containing 16
RGD ID: 1352454
HGNC Page HGNC:12930
Description: Enables several functions, including DNA-binding transcription repressor activity, RNA polymerase II-specific; protein homodimerization activity; and transcription corepressor binding activity. Involved in several processes, including positive regulation of cell differentiation; positive regulation of ossification; and regulation of DNA-templated transcription. Acts upstream of or within negative regulation of DNA-templated transcription. Located in PML body and nuclear speck. Part of transcription repressor complex. Implicated in acute promyelocytic leukemia.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: PLZF; promyelocytic leukaemia zinc finger; zinc finger and BTB domain-containing protein 16; zinc finger protein 145 (Kruppel-like, expressed in promyelocytic leukemia); zinc finger protein PLZF; ZNF145
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
GRCh3811114,059,711 - 114,256,770 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl11114,059,041 - 114,256,765 (+)EnsemblGRCh38hg38GRCh38
GRCh3711113,930,433 - 114,127,492 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3611113,435,641 - 113,626,608 (+)NCBINCBI36Build 36hg18NCBI36
Build 3411113,435,658 - 113,626,568NCBI
Celera11111,083,317 - 111,274,300 (+)NCBICelera
Cytogenetic Map11q23.2NCBI
HuRef11109,859,046 - 110,049,950 (+)NCBIHuRef
CHM1_111113,814,520 - 114,005,500 (+)NCBICHM1_1
T2T-CHM13v2.011114,070,066 - 114,267,135 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(1->4)-beta-D-glucan  (ISO)
1-naphthyl isothiocyanate  (ISO)
17beta-estradiol  (EXP,ISO)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3,7-dihydropurine-6-thione  (ISO)
3-chloropropane-1,2-diol  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-sulfonyldiphenol  (EXP,ISO)
4-amino-2,6-dinitrotoluene  (ISO)
4-hydroxyphenyl retinamide  (ISO)
6-propyl-2-thiouracil  (ISO)
acrylamide  (EXP,ISO)
Aflatoxin B2 alpha  (EXP)
aldehydo-D-glucose  (ISO)
all-trans-retinoic acid  (EXP)
allethrin  (ISO)
amoxicillin  (ISO)
amphotericin B  (EXP)
arsane  (ISO)
arsenic atom  (ISO)
Benoxacor  (ISO)
benzo[a]pyrene  (EXP)
beta-naphthoflavone  (ISO)
bexarotene  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bromobenzene  (ISO)
busulfan  (ISO)
buta-1,3-diene  (ISO)
butan-1-ol  (EXP)
C60 fullerene  (ISO)
cadmium atom  (ISO)
cadmium dichloride  (ISO)
carbamazepine  (ISO)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chloroprene  (ISO)
chlorpyrifos  (ISO)
choline  (ISO)
cisplatin  (EXP)
cocaine  (ISO)
crocidolite asbestos  (ISO)
Cuprizon  (ISO)
cyclosporin A  (EXP,ISO)
cyhalothrin  (ISO)
cypermethrin  (ISO)
cyproconazole  (ISO)
D-glucose  (ISO)
dexamethasone  (EXP)
dibenz[a,h]anthracene  (ISO)
dibutyl phthalate  (ISO)
dichloroacetic acid  (ISO)
dieldrin  (ISO)
diethylstilbestrol  (ISO)
dimethylarsinic acid  (ISO)
dioxygen  (EXP)
diquat  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP,ISO)
ellagic acid  (EXP)
endosulfan  (ISO)
entinostat  (EXP)
epoxiconazole  (ISO)
ethanol  (EXP,ISO)
fenvalerate  (ISO)
flusilazole  (ISO)
folic acid  (ISO)
fructose  (ISO)
fulvestrant  (EXP)
furan  (ISO)
glucose  (ISO)
glycidol  (ISO)
GW 4064  (ISO)
hexaconazole  (ISO)
indole-3-methanol  (ISO)
indometacin  (EXP)
isoprenaline  (ISO)
isotretinoin  (EXP)
L-methionine  (ISO)
lipopolysaccharide  (EXP)
medroxyprogesterone acetate  (EXP)
mercaptopurine  (ISO)
mercury atom  (EXP)
mercury dibromide  (EXP)
mercury dichloride  (ISO)
mercury(0)  (EXP)
metformin  (ISO)
methoxychlor  (ISO)
methylarsonic acid  (ISO)
methylmercury chloride  (EXP)
mono(2-ethylhexyl) phthalate  (ISO)
N-acetyl-L-cysteine  (ISO)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
nickel sulfate  (ISO)
ozone  (ISO)
p-chloromercuribenzoic acid  (EXP)
panobinostat  (EXP)
paracetamol  (EXP,ISO)
paraquat  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenformin  (ISO)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
pirinixic acid  (ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
progesterone  (EXP,ISO)
propiconazole  (ISO)
purine-6-thiol  (ISO)
resmethrin  (ISO)
resveratrol  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
silicon dioxide  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (EXP,ISO)
stigmasterol  (ISO)
tamibarotene  (EXP)
tamoxifen  (ISO)
testosterone  (ISO)
tetrachloroethene  (ISO)
tetrachloromethane  (ISO)
tetraphene  (ISO)
titanium dioxide  (ISO)
tremolite asbestos  (ISO)
tributylstannane  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
triphenylstannane  (ISO)
troglitazone  (ISO)
uranium atom  (ISO)
valproic acid  (EXP,ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
anterior/posterior pattern specification  (IEA,ISO)
apoptotic process  (NAS)
cartilage development  (IDA)
cell population proliferation  (IEA,ISO)
central nervous system development  (IEA,ISS)
embryonic digit morphogenesis  (IEA,ISO)
embryonic hindlimb morphogenesis  (IEA,ISO)
embryonic limb morphogenesis  (ISO)
embryonic pattern specification  (IEA,ISO)
forelimb morphogenesis  (IEA,ISO)
hemopoiesis  (IDA,IEA,TAS)
hindlimb morphogenesis  (IEA,ISO)
male germ-line stem cell asymmetric division  (IEA,ISO)
mesonephros development  (IEA,ISS)
myeloid cell differentiation  (TAS)
negative regulation of cell population proliferation  (IEA,ISO)
negative regulation of DNA-templated transcription  (IDA,NAS)
negative regulation of myeloid cell differentiation  (IEA,ISS)
negative regulation of transcription by RNA polymerase II  (IDA)
ossification involved in bone maturation  (IEA,ISO)
positive regulation of apoptotic process  (IEA,ISO)
positive regulation of cartilage development  (IDA)
positive regulation of chondrocyte differentiation  (IMP)
positive regulation of DNA-templated transcription  (IDA)
positive regulation of fat cell differentiation  (IMP)
positive regulation of NK T cell differentiation  (IEA)
positive regulation of ossification  (IDA)
positive regulation of transcription by RNA polymerase II  (IEA)
protein localization to nucleus  (IEA,ISO)
protein ubiquitination  (IEA)
regulation of DNA-templated transcription  (IEA,ISO)
regulation of transcription by RNA polymerase II  (IBA,IEA)
skeletal system development  (IEA,ISO)

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia. Chen SJ, etal., J Clin Invest. 1993 May;91(5):2260-7.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. Deletion of a conserved noncoding sequence in Plzf intron leads to Plzf down-regulation in limb bud and polydactyly in the rat. Liska F, etal., Dev Dyn. 2009 Mar;238(3):673-84.
4. Targeting of the Plzf Gene in the Rat by Transcription Activator-Like Effector Nuclease Results in Caudal Regression Syndrome in Spontaneously Hypertensive Rats. Liška F, etal., PLoS One. 2016 Oct 11;11(10):e0164206. doi: 10.1371/journal.pone.0164206. eCollection 2016.
5. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
6. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
7. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
8. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
9. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
10. An ATIPical family of angiotensin II AT2 receptor-interacting proteins. Rodrigues-Ferreira S and Nahmias C, Trends Endocrinol Metab. 2010 Nov;21(11):684-90.
Additional References at PubMed
PMID:8384553   PMID:8541544   PMID:8622986   PMID:8889548   PMID:9256429   PMID:9294197   PMID:9486654   PMID:9531570   PMID:9627120   PMID:9765306   PMID:9770450   PMID:10433962  
PMID:10497277   PMID:10500192   PMID:10537309   PMID:10572087   PMID:10688654   PMID:10791968   PMID:10980608   PMID:11090081   PMID:11106752   PMID:11161217   PMID:11175338   PMID:11719366  
PMID:11865059   PMID:11920278   PMID:11929873   PMID:11964310   PMID:12004059   PMID:12145280   PMID:12242665   PMID:12408802   PMID:12460926   PMID:12477932   PMID:12590135   PMID:12802276  
PMID:12821938   PMID:12970399   PMID:14521715   PMID:14527952   PMID:14597771   PMID:14645547   PMID:14657020   PMID:14702039   PMID:14982881   PMID:15065091   PMID:15077196   PMID:15196694  
PMID:15219838   PMID:15231748   PMID:15467736   PMID:15489334   PMID:15623533   PMID:15949438   PMID:15964811   PMID:15968309   PMID:16024608   PMID:16169070   PMID:16189514   PMID:16637071  
PMID:16676348   PMID:16828757   PMID:17082479   PMID:17118363   PMID:17340613   PMID:17498654   PMID:17500595   PMID:17515885   PMID:17537403   PMID:17881917   PMID:18000064   PMID:18029348  
PMID:18262754   PMID:18348865   PMID:18417445   PMID:18448589   PMID:18504436   PMID:18568019   PMID:18611983   PMID:18703361   PMID:18771349   PMID:18846501   PMID:18953495   PMID:19421145  
PMID:19444914   PMID:19451220   PMID:19648967   PMID:19723763   PMID:19762545   PMID:19796243   PMID:19855079   PMID:19913121   PMID:20010871   PMID:20038602   PMID:20098615   PMID:20211142  
PMID:20379614   PMID:20628086   PMID:20945532   PMID:21547890   PMID:21632718   PMID:21873635   PMID:21900206   PMID:21915328   PMID:21988832   PMID:22292015   PMID:22555178   PMID:23088713  
PMID:23223428   PMID:23280881   PMID:23333304   PMID:23414517   PMID:23416030   PMID:23798432   PMID:23804241   PMID:23898169   PMID:24339862   PMID:24348178   PMID:24359167   PMID:24359566  
PMID:24416448   PMID:24424509   PMID:24764561   PMID:24784718   PMID:24816988   PMID:24821727   PMID:24821728   PMID:24990570   PMID:25023763   PMID:25178676   PMID:25241761   PMID:25369784  
PMID:25416956   PMID:25447205   PMID:25705792   PMID:25760953   PMID:25807461   PMID:25808865   PMID:25833398   PMID:26121690   PMID:26186194   PMID:26264872   PMID:26297253   PMID:26676652  
PMID:26871637   PMID:26916077   PMID:27035670   PMID:27107012   PMID:28038473   PMID:28223321   PMID:28416638   PMID:28514442   PMID:28581124   PMID:28611215   PMID:28786561   PMID:28948827  
PMID:29186366   PMID:29317492   PMID:29358655   PMID:29425303   PMID:29997244   PMID:30246336   PMID:30431129   PMID:30672466   PMID:31065369   PMID:31087222   PMID:31126665   PMID:31378879  
PMID:31554695   PMID:32296183   PMID:32517789   PMID:32773339   PMID:32814053   PMID:33060197   PMID:33206504   PMID:33470442   PMID:33961781   PMID:34042280   PMID:34660783   PMID:34764413  
PMID:35641094   PMID:36216898   PMID:36768269   PMID:36931259   PMID:38287116   PMID:38373386  


Genomics

Comparative Map Data
ZBTB16
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3811114,059,711 - 114,256,770 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl11114,059,041 - 114,256,765 (+)EnsemblGRCh38hg38GRCh38
GRCh3711113,930,433 - 114,127,492 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3611113,435,641 - 113,626,608 (+)NCBINCBI36Build 36hg18NCBI36
Build 3411113,435,658 - 113,626,568NCBI
Celera11111,083,317 - 111,274,300 (+)NCBICelera
Cytogenetic Map11q23.2NCBI
HuRef11109,859,046 - 110,049,950 (+)NCBIHuRef
CHM1_111113,814,520 - 114,005,500 (+)NCBICHM1_1
T2T-CHM13v2.011114,070,066 - 114,267,135 (+)NCBIT2T-CHM13v2.0
Zbtb16
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39948,563,097 - 48,747,525 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl948,565,597 - 48,747,522 (-)EnsemblGRCm39 Ensembl
GRCm38948,651,797 - 48,836,225 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl948,654,297 - 48,836,222 (-)EnsemblGRCm38mm10GRCm38
MGSCv37948,462,402 - 48,644,050 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36948,406,264 - 48,587,864 (-)NCBIMGSCv36mm8
Celera945,948,793 - 46,132,024 (-)NCBICelera
Cytogenetic Map9A5.3NCBI
cM Map926.47NCBI
Zbtb16
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8857,885,886 - 58,073,507 (-)NCBIGRCr8
mRatBN7.2848,989,376 - 49,177,011 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl848,994,566 - 49,177,011 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx854,500,313 - 54,682,843 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0852,779,162 - 52,961,700 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0850,643,426 - 50,825,960 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0852,980,226 - 53,146,765 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl852,985,313 - 53,146,953 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0851,573,252 - 51,740,759 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4851,931,530 - 52,094,813 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1852,110,091 - 52,110,396 (-)NCBI
Celera848,553,034 - 48,734,595 (-)NCBICelera
Cytogenetic Map8q23NCBI
Zbtb16
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541215,668,332 - 15,845,372 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495541215,668,332 - 15,845,384 (+)NCBIChiLan1.0ChiLan1.0
ZBTB16
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v29114,803,098 - 114,998,525 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan111115,897,024 - 116,092,398 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v011108,938,414 - 109,133,819 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.111112,780,446 - 112,977,164 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl11112,780,380 - 112,977,164 (+)Ensemblpanpan1.1panPan2
ZBTB16
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1519,082,594 - 19,284,360 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl519,087,154 - 19,267,628 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha519,007,960 - 19,195,854 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0519,104,312 - 19,292,747 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl519,106,853 - 19,291,539 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1519,168,970 - 19,356,857 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0519,070,647 - 19,258,747 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0519,117,162 - 19,305,163 (-)NCBIUU_Cfam_GSD_1.0
Zbtb16
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494796,135,014 - 96,315,732 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936612395,177 - 570,595 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936612389,877 - 570,595 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZBTB16
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl941,639,701 - 41,836,742 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1941,639,536 - 41,839,254 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2946,454,490 - 46,459,483 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ZBTB16
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11105,446,067 - 105,648,771 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1105,449,994 - 105,643,344 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604320,384,628 - 20,582,116 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Zbtb16
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247849,546,509 - 9,726,960 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247849,545,529 - 9,726,960 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZBTB16
84 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_006006.6(ZBTB16):c.1849A>G (p.Met617Val) single nucleotide variant Skeletal defects, genital hypoplasia, and intellectual disability [RCV000014305] Chr11:114250382 [GRCh38]
Chr11:114121104 [GRCh37]
Chr11:11q23.2
pathogenic|uncertain significance
GRCh38/hg38 11q23.2-23.3(chr11:113444446-120648921)x3 copy number gain See cases [RCV000050627] Chr11:113444446..120648921 [GRCh38]
Chr11:113315168..120519630 [GRCh37]
Chr11:112820378..120024840 [NCBI36]
Chr11:11q23.2-23.3
pathogenic
GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3 copy number gain See cases [RCV000053638] Chr11:100348599..135040246 [GRCh38]
Chr11:100219331..134910140 [GRCh37]
Chr11:99724541..134415350 [NCBI36]
Chr11:11q22.1-25
pathogenic
NM_006006.4(ZBTB16):c.1528G>A (p.Glu510Lys) single nucleotide variant Malignant melanoma [RCV000062128] Chr11:114242241 [GRCh38]
Chr11:114112963 [GRCh37]
Chr11:113618173 [NCBI36]
Chr11:11q23.2
not provided
NM_006006.4(ZBTB16):c.1200G>T (p.Arg400=) single nucleotide variant Lung cancer [RCV000109611] Chr11:114064500 [GRCh38]
Chr11:113935222 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.4(ZBTB16):c.1268+11773T>C single nucleotide variant Lung cancer [RCV000109612] Chr11:114076341 [GRCh38]
Chr11:113947063 [GRCh37]
Chr11:11q23.2
uncertain significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3
pathogenic
GRCh38/hg38 11q23.2-25(chr11:112864326-131189315)x3 copy number gain See cases [RCV000137582] Chr11:112864326..131189315 [GRCh38]
Chr11:112832130..131059210 [GRCh37]
Chr11:112240259..130564420 [NCBI36]
Chr11:11q23.2-25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
NM_006006.6(ZBTB16):c.1229G>A (p.Gly410Glu) single nucleotide variant Inborn genetic diseases [RCV003261211] Chr11:114064529 [GRCh38]
Chr11:113935251 [GRCh37]
Chr11:11q23.2
uncertain significance
GRCh37/hg19 11q13.4-23.3(chr11:71588805-116680918)x3 copy number gain not provided [RCV000683374] Chr11:71588805..116680918 [GRCh37]
Chr11:11q13.4-23.3
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
NM_006006.6(ZBTB16):c.1624+7C>G single nucleotide variant not provided [RCV000921846] Chr11:114242344 [GRCh38]
Chr11:114113066 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1293G>A (p.Thr431=) single nucleotide variant not provided [RCV000905823] Chr11:114156361 [GRCh38]
Chr11:114027083 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1072G>A (p.Val358Met) single nucleotide variant ZBTB16-related condition [RCV003905910]|not provided [RCV000966396] Chr11:114064372 [GRCh38]
Chr11:113935094 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.426C>T (p.Ala142=) single nucleotide variant not provided [RCV000926381] Chr11:114063726 [GRCh38]
Chr11:113934448 [GRCh37]
Chr11:11q23.2
benign|likely benign
NM_006006.6(ZBTB16):c.939C>T (p.Gly313=) single nucleotide variant not provided [RCV000898417] Chr11:114064239 [GRCh38]
Chr11:113934961 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.780C>T (p.Ala260=) single nucleotide variant not provided [RCV000921061] Chr11:114064080 [GRCh38]
Chr11:113934802 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.672C>G (p.Pro224=) single nucleotide variant not provided [RCV000906103] Chr11:114063972 [GRCh38]
Chr11:113934694 [GRCh37]
Chr11:11q23.2
benign
NM_006006.6(ZBTB16):c.813G>A (p.Lys271=) single nucleotide variant not provided [RCV000906642] Chr11:114064113 [GRCh38]
Chr11:113934835 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.756C>T (p.Pro252=) single nucleotide variant not provided [RCV000916114] Chr11:114064056 [GRCh38]
Chr11:113934778 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1883C>T (p.Ser628Leu) single nucleotide variant not provided [RCV000994728] Chr11:114250416 [GRCh38]
Chr11:114121138 [GRCh37]
Chr11:11q23.2
uncertain significance
GRCh37/hg19 11q22.3-23.3(chr11:104101411-116680918)x1 copy number loss not provided [RCV000848741] Chr11:104101411..116680918 [GRCh37]
Chr11:11q22.3-23.3
pathogenic
GRCh37/hg19 11q22.3-23.2(chr11:103320065-114349787)x1 copy number loss not provided [RCV001006439] Chr11:103320065..114349787 [GRCh37]
Chr11:11q22.3-23.2
pathogenic
GRCh37/hg19 11q23.1-23.3(chr11:110969076-114578509)x1 copy number loss not provided [RCV000848936] Chr11:110969076..114578509 [GRCh37]
Chr11:11q23.1-23.3
uncertain significance
GRCh37/hg19 11q22.3-23.3(chr11:105699599-114524876)x1 copy number loss not provided [RCV001006445] Chr11:105699599..114524876 [GRCh37]
Chr11:11q22.3-23.3
pathogenic
NM_006006.6(ZBTB16):c.1030G>A (p.Ala344Thr) single nucleotide variant Inborn genetic diseases [RCV003273674] Chr11:114064330 [GRCh38]
Chr11:113935052 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.672C>T (p.Pro224=) single nucleotide variant not provided [RCV000899996] Chr11:114063972 [GRCh38]
Chr11:113934694 [GRCh37]
Chr11:11q23.2
benign
NM_006006.6(ZBTB16):c.1176T>C (p.Ala392=) single nucleotide variant not provided [RCV000919355] Chr11:114064476 [GRCh38]
Chr11:113935198 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1542C>T (p.Gly514=) single nucleotide variant not provided [RCV000952970] Chr11:114242255 [GRCh38]
Chr11:114112977 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1005C>T (p.Ser335=) single nucleotide variant not provided [RCV000906600] Chr11:114064305 [GRCh38]
Chr11:113935027 [GRCh37]
Chr11:11q23.2
benign
NM_006006.6(ZBTB16):c.1047G>A (p.Pro349=) single nucleotide variant not provided [RCV000913078] Chr11:114064347 [GRCh38]
Chr11:113935069 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.261A>G (p.Ala87=) single nucleotide variant not provided [RCV000935866] Chr11:114063561 [GRCh38]
Chr11:113934283 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.402G>A (p.Glu134=) single nucleotide variant not provided [RCV000933906] Chr11:114063702 [GRCh38]
Chr11:113934424 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.399G>A (p.Thr133=) single nucleotide variant not provided [RCV000957004] Chr11:114063699 [GRCh38]
Chr11:113934421 [GRCh37]
Chr11:11q23.2
benign
NM_006006.6(ZBTB16):c.1248C>T (p.Asn416=) single nucleotide variant not provided [RCV000890014] Chr11:114064548 [GRCh38]
Chr11:113935270 [GRCh37]
Chr11:11q23.2
benign
NC_000011.9:g.104288964_134937416dup duplication Distal trisomy 11q [RCV001250234] Chr11:104288964..134937416 [GRCh37]
Chr11:11q22.3-25
pathogenic
NM_006006.6(ZBTB16):c.1998G>A (p.Thr666=) single nucleotide variant not provided [RCV001816109] Chr11:114250531 [GRCh38]
Chr11:114121253 [GRCh37]
Chr11:11q23.2
likely benign
GRCh37/hg19 11q23.1-24.3(chr11:112375478-128785742)x3 copy number gain not provided [RCV001829187] Chr11:112375478..128785742 [GRCh37]
Chr11:11q23.1-24.3
pathogenic
GRCh37/hg19 11q14.1-23.3(chr11:85422071-118022671)x1 copy number loss not provided [RCV001832892] Chr11:85422071..118022671 [GRCh37]
Chr11:11q14.1-23.3
uncertain significance
NM_006006.6(ZBTB16):c.443G>A (p.Arg148His) single nucleotide variant Inborn genetic diseases [RCV003101387]|See cases [RCV002252467] Chr11:114063743 [GRCh38]
Chr11:113934465 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.977C>T (p.Pro326Leu) single nucleotide variant Inborn genetic diseases [RCV003255581] Chr11:114064277 [GRCh38]
Chr11:113934999 [GRCh37]
Chr11:11q23.2
uncertain significance
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25
pathogenic
GRCh37/hg19 11q22.3-23.3(chr11:109328787-116414966)x1 copy number loss not provided [RCV002474547] Chr11:109328787..116414966 [GRCh37]
Chr11:11q22.3-23.3
pathogenic
NM_006006.6(ZBTB16):c.590G>A (p.Ser197Asn) single nucleotide variant Inborn genetic diseases [RCV002753540] Chr11:114063890 [GRCh38]
Chr11:113934612 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.457C>G (p.Leu153Val) single nucleotide variant Inborn genetic diseases [RCV002905756] Chr11:114063757 [GRCh38]
Chr11:113934479 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.1303G>A (p.Glu435Lys) single nucleotide variant Inborn genetic diseases [RCV002762486] Chr11:114156371 [GRCh38]
Chr11:114027093 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.1006G>A (p.Val336Met) single nucleotide variant Inborn genetic diseases [RCV002759182] Chr11:114064306 [GRCh38]
Chr11:113935028 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.1084C>A (p.Leu362Met) single nucleotide variant Inborn genetic diseases [RCV002783738] Chr11:114064384 [GRCh38]
Chr11:113935106 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.728C>T (p.Thr243Met) single nucleotide variant Inborn genetic diseases [RCV002744676] Chr11:114064028 [GRCh38]
Chr11:113934750 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.704A>G (p.His235Arg) single nucleotide variant Inborn genetic diseases [RCV002808686] Chr11:114064004 [GRCh38]
Chr11:113934726 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.1222G>A (p.Val408Met) single nucleotide variant Inborn genetic diseases [RCV002724912] Chr11:114064522 [GRCh38]
Chr11:113935244 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.772G>A (p.Gly258Arg) single nucleotide variant Inborn genetic diseases [RCV003179430] Chr11:114064072 [GRCh38]
Chr11:113934794 [GRCh37]
Chr11:11q23.2
uncertain significance
NM_006006.6(ZBTB16):c.414C>T (p.Ala138=) single nucleotide variant not provided [RCV003398138] Chr11:114063714 [GRCh38]
Chr11:113934436 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1269-3228A>G single nucleotide variant not provided [RCV003398139] Chr11:114153109 [GRCh38]
Chr11:114023831 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1626C>T (p.Gly542=) single nucleotide variant not provided [RCV003398140] Chr11:114247199 [GRCh38]
Chr11:114117921 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1183A>G (p.Met395Val) single nucleotide variant Inborn genetic diseases [RCV003366066] Chr11:114064483 [GRCh38]
Chr11:113935205 [GRCh37]
Chr11:11q23.2
uncertain significance
Single allele duplication not provided [RCV003448710] Chr11:102134973..134945611 [GRCh37]
Chr11:11q22.2-25
pathogenic
NM_006006.6(ZBTB16):c.90C>T (p.Ala30=) single nucleotide variant not provided [RCV003410920] Chr11:114063390 [GRCh38]
Chr11:113934112 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.31C>T (p.Leu11=) single nucleotide variant ZBTB16-related condition [RCV003909675] Chr11:114063331 [GRCh38]
Chr11:113934053 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1398C>T (p.Cys466=) single nucleotide variant ZBTB16-related condition [RCV003964152] Chr11:114186983 [GRCh38]
Chr11:114057705 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.565A>G (p.Thr189Ala) single nucleotide variant ZBTB16-related condition [RCV003971725] Chr11:114063865 [GRCh38]
Chr11:113934587 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.2004C>T (p.Leu668=) single nucleotide variant ZBTB16-related condition [RCV003947195] Chr11:114250537 [GRCh38]
Chr11:114121259 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.207C>T (p.His69=) single nucleotide variant ZBTB16-related condition [RCV003958974] Chr11:114063507 [GRCh38]
Chr11:113934229 [GRCh37]
Chr11:11q23.2
likely benign
NM_006006.6(ZBTB16):c.1029C>T (p.Asp343=) single nucleotide variant ZBTB16-related condition [RCV003949659] Chr11:114064329 [GRCh38]
Chr11:113935051 [GRCh37]
Chr11:11q23.2
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2075
Count of miRNA genes:820
Interacting mature miRNAs:975
Transcripts:ENST00000335953, ENST00000392996, ENST00000535379, ENST00000535509, ENST00000535700, ENST00000539918, ENST00000541602, ENST00000544220, ENST00000545851
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
D11S1792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711114,078,140 - 114,078,408UniSTSGRCh37
Build 3611113,583,350 - 113,583,618RGDNCBI36
Celera11111,231,047 - 111,231,315RGD
Cytogenetic Map11q23.1UniSTS
HuRef11110,006,698 - 110,006,966UniSTS
Marshfield Genetic Map11107.45UniSTS
Marshfield Genetic Map11107.45RGD
Genethon Genetic Map11112.7UniSTS
deCODE Assembly Map11114.7UniSTS
D11S1191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711114,092,188 - 114,092,468UniSTSGRCh37
Build 3611113,597,398 - 113,597,678RGDNCBI36
Celera11111,245,095 - 111,245,375RGD
Cytogenetic Map11q23.1UniSTS
HuRef11110,020,746 - 110,021,026UniSTS
D11S1104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711114,031,194 - 114,031,448UniSTSGRCh37
Build 3611113,536,404 - 113,536,658RGDNCBI36
Celera11111,184,105 - 111,184,359RGD
Cytogenetic Map11q23.1UniSTS
HuRef11109,959,755 - 109,960,009UniSTS
RH16530  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711113,952,572 - 113,952,705UniSTSGRCh37
Build 3611113,457,782 - 113,457,915RGDNCBI36
Celera11111,105,457 - 111,105,590RGD
Cytogenetic Map11q23.1UniSTS
HuRef11109,881,186 - 109,881,319UniSTS
GeneMap99-GB4 RH Map11373.7UniSTS
UniSTS:99119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711113,934,145 - 113,934,359UniSTSGRCh37
Build 3611113,439,355 - 113,439,569RGDNCBI36
Celera11111,087,032 - 111,087,246RGD
HuRef11109,862,761 - 109,862,975UniSTS
UniSTS:99223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711114,117,921 - 114,118,083UniSTSGRCh37
Build 3611113,623,131 - 113,623,293RGDNCBI36
Celera11111,270,813 - 111,270,975RGD
HuRef11110,046,461 - 110,046,623UniSTS
SHGC-80797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711113,973,698 - 113,973,977UniSTSGRCh37
Build 3611113,478,908 - 113,479,187RGDNCBI36
Celera11111,126,579 - 111,126,858RGD
Cytogenetic Map11q23.1UniSTS
HuRef11109,902,310 - 109,902,589UniSTS
TNG Radiation Hybrid Map1152603.0UniSTS
D11S2076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711114,096,655 - 114,096,778UniSTSGRCh37
Build 3611113,601,865 - 113,601,988RGDNCBI36
Celera11111,249,562 - 111,249,685RGD
Cytogenetic Map11q23.1UniSTS
HuRef11110,025,213 - 110,025,336UniSTS
D11S3293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711114,117,790 - 114,118,079UniSTSGRCh37
Build 3611113,623,000 - 113,623,289RGDNCBI36
Celera11111,270,682 - 111,270,971RGD
Cytogenetic Map11q23.1UniSTS
HuRef11110,046,330 - 110,046,619UniSTS
D11S3462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711113,997,012 - 113,997,163UniSTSGRCh37
Build 3611113,502,222 - 113,502,373RGDNCBI36
Celera11111,149,893 - 111,150,044RGD
Cytogenetic Map11q23.1UniSTS
HuRef11109,925,548 - 109,925,699UniSTS
A008C32  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711113,952,567 - 113,952,699UniSTSGRCh37
Build 3611113,457,777 - 113,457,909RGDNCBI36
Celera11111,105,452 - 111,105,584RGD
Cytogenetic Map11q23.1UniSTS
HuRef11109,881,181 - 109,881,313UniSTS
GeneMap99-GB4 RH Map11373.28UniSTS
ZBTB16_8745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711114,121,046 - 114,121,560UniSTSGRCh37
GRCh371938,055,082 - 38,056,004UniSTSGRCh37
Build 3611113,626,256 - 113,626,770RGDNCBI36
Celera1934,855,764 - 34,856,686UniSTS
Celera11111,273,948 - 111,274,462RGD
HuRef11110,049,598 - 110,050,112UniSTS
HuRef1934,505,175 - 34,506,097UniSTS
ZNF145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711113,934,910 - 113,935,029UniSTSGRCh37
Build 3611113,440,120 - 113,440,239RGDNCBI36
Celera11111,087,797 - 111,087,916RGD
Cytogenetic Map11q23.1UniSTS
HuRef11109,863,526 - 109,863,645UniSTS
GeneMap99-GB4 RH Map11373.28UniSTS
SHGC-33207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711113,952,661 - 113,952,810UniSTSGRCh37
Build 3611113,457,871 - 113,458,020RGDNCBI36
Celera11111,105,546 - 111,105,695RGD
Cytogenetic Map11q23.1UniSTS
HuRef11109,881,275 - 109,881,424UniSTS
TNG Radiation Hybrid Map1152592.0UniSTS
GeneMap99-G3 RH Map115050.0UniSTS
D11S4022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711114,017,857 - 114,018,059UniSTSGRCh37
Build 3611113,523,067 - 113,523,269RGDNCBI36
Celera11111,170,736 - 111,170,938RGD
Cytogenetic Map11q23.1UniSTS
HuRef11109,946,392 - 109,946,594UniSTS
Whitehead-RH Map11513.8UniSTS
Whitehead-YAC Contig Map11 UniSTS
NCBI RH Map111009.2UniSTS
GDB:335751  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map10q24.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map3q22.2UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map6p21.1-p12.2UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map13q12.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map9q22.32UniSTS
fj34c06.x1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711113,982,251 - 113,983,407UniSTSGRCh37
Celera11111,135,132 - 111,136,288UniSTS
HuRef11109,910,863 - 109,912,019UniSTS


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 1637 1986 898 170 462 77 3648 1699 1087 65 697 1076 92 1097 2543 1
Low 610 972 763 398 856 329 428 455 2559 256 572 301 73 1 107 244 3 1
Below cutoff 139 33 57 49 222 52 255 34 82 80 135 188 8 1 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001018011 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354750 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354752 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_006006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005271658 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054369888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054369889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054369890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001747955 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB208916 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF060568 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH006378 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000908 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP002518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP002755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC026902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC029812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM969145 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648973 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  S60093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z19002 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000335953   ⟹   ENSP00000338157
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,059,711 - 114,256,765 (+)Ensembl
RefSeq Acc Id: ENST00000392996   ⟹   ENSP00000376721
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,060,507 - 114,250,652 (+)Ensembl
RefSeq Acc Id: ENST00000535379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,237,207 - 114,250,557 (+)Ensembl
RefSeq Acc Id: ENST00000535509
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,246,790 - 114,250,476 (+)Ensembl
RefSeq Acc Id: ENST00000535700   ⟹   ENSP00000443013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,060,204 - 114,066,138 (+)Ensembl
RefSeq Acc Id: ENST00000539918   ⟹   ENSP00000445047
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,064,412 - 114,247,344 (+)Ensembl
RefSeq Acc Id: ENST00000541602
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,059,725 - 114,189,764 (+)Ensembl
RefSeq Acc Id: ENST00000544220   ⟹   ENSP00000437716
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,059,737 - 114,063,646 (+)Ensembl
RefSeq Acc Id: ENST00000545851
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,180,766 - 114,247,296 (+)Ensembl
RefSeq Acc Id: ENST00000682218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,183,380 - 114,252,357 (+)Ensembl
RefSeq Acc Id: ENST00000682278   ⟹   ENSP00000506794
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,059,041 - 114,252,357 (+)Ensembl
RefSeq Acc Id: ENST00000682697   ⟹   ENSP00000506924
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,062,220 - 114,252,357 (+)Ensembl
RefSeq Acc Id: ENST00000682810   ⟹   ENSP00000507219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,059,714 - 114,252,357 (+)Ensembl
RefSeq Acc Id: ENST00000682971   ⟹   ENSP00000506894
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,061,052 - 114,252,357 (+)Ensembl
RefSeq Acc Id: ENST00000683006
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,160,427 - 114,256,764 (+)Ensembl
RefSeq Acc Id: ENST00000683233   ⟹   ENSP00000506995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,059,714 - 114,252,357 (+)Ensembl
RefSeq Acc Id: ENST00000683318   ⟹   ENSP00000508351
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,060,204 - 114,252,357 (+)Ensembl
RefSeq Acc Id: ENST00000683554   ⟹   ENSP00000506953
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,062,226 - 114,252,357 (+)Ensembl
RefSeq Acc Id: ENST00000684295   ⟹   ENSP00000507788
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,059,881 - 114,252,357 (+)Ensembl
RefSeq Acc Id: ENST00000684612   ⟹   ENSP00000507350
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11114,059,714 - 114,252,357 (+)Ensembl
RefSeq Acc Id: NM_001018011   ⟹   NP_001018011
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,060,507 - 114,256,765 (+)NCBI
GRCh3711113,930,289 - 114,126,702 (+)NCBI
Build 3611113,436,498 - 113,626,608 (+)NCBI Archive
HuRef11109,859,046 - 110,049,950 (+)ENTREZGENE
CHM1_111113,815,377 - 114,005,500 (+)NCBI
T2T-CHM13v2.011114,070,862 - 114,267,130 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001354750   ⟹   NP_001341679
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,059,711 - 114,256,765 (+)NCBI
T2T-CHM13v2.011114,070,066 - 114,267,130 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001354751   ⟹   NP_001341680
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,060,242 - 114,256,765 (+)NCBI
T2T-CHM13v2.011114,070,597 - 114,267,130 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001354752   ⟹   NP_001341681
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,063,211 - 114,256,770 (+)NCBI
T2T-CHM13v2.011114,073,567 - 114,267,135 (+)NCBI
Sequence:
RefSeq Acc Id: NM_006006   ⟹   NP_005997
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,059,711 - 114,256,765 (+)NCBI
GRCh3711113,930,289 - 114,126,702 (+)NCBI
Build 3611113,435,641 - 113,626,608 (+)NCBI Archive
HuRef11109,859,046 - 110,049,950 (+)ENTREZGENE
CHM1_111113,814,520 - 114,005,500 (+)NCBI
T2T-CHM13v2.011114,070,066 - 114,267,130 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005271658   ⟹   XP_005271715
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,059,711 - 114,210,332 (+)NCBI
GRCh3711113,930,289 - 114,126,702 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047427563   ⟹   XP_047283519
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,059,711 - 114,121,896 (+)NCBI
RefSeq Acc Id: XM_054369888   ⟹   XP_054225863
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011114,072,576 - 114,267,130 (+)NCBI
RefSeq Acc Id: XM_054369889   ⟹   XP_054225864
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011114,070,066 - 114,221,344 (+)NCBI
RefSeq Acc Id: XM_054369890   ⟹   XP_054225865
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011114,070,066 - 114,132,249 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001018011 (Get FASTA)   NCBI Sequence Viewer  
  NP_001341679 (Get FASTA)   NCBI Sequence Viewer  
  NP_001341680 (Get FASTA)   NCBI Sequence Viewer  
  NP_001341681 (Get FASTA)   NCBI Sequence Viewer  
  NP_005997 (Get FASTA)   NCBI Sequence Viewer  
  XP_005271715 (Get FASTA)   NCBI Sequence Viewer  
  XP_047283519 (Get FASTA)   NCBI Sequence Viewer  
  XP_054225863 (Get FASTA)   NCBI Sequence Viewer  
  XP_054225864 (Get FASTA)   NCBI Sequence Viewer  
  XP_054225865 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC32847 (Get FASTA)   NCBI Sequence Viewer  
  AAC60590 (Get FASTA)   NCBI Sequence Viewer  
  AAD03619 (Get FASTA)   NCBI Sequence Viewer  
  AAH26902 (Get FASTA)   NCBI Sequence Viewer  
  AAH29812 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33858 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33859 (Get FASTA)   NCBI Sequence Viewer  
  BAD92153 (Get FASTA)   NCBI Sequence Viewer  
  CAA79489 (Get FASTA)   NCBI Sequence Viewer  
  EAW67241 (Get FASTA)   NCBI Sequence Viewer  
  EAW67242 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000338157
  ENSP00000338157.4
  ENSP00000376721
  ENSP00000376721.2
  ENSP00000437716.1
  ENSP00000445047.1
  ENSP00000506794.1
  ENSP00000506894.1
  ENSP00000506924.1
  ENSP00000506953.1
  ENSP00000506995.1
  ENSP00000507219
  ENSP00000507219.1
  ENSP00000507350.1
  ENSP00000507788
  ENSP00000507788.1
  ENSP00000508351
  ENSP00000508351.1
GenBank Protein Q05516 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_005997   ⟸   NM_006006
- Peptide Label: isoform 1
- UniProtKB: Q8TAL4 (UniProtKB/Swiss-Prot),   Q05516 (UniProtKB/Swiss-Prot),   A0A024R3C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001018011   ⟸   NM_001018011
- Peptide Label: isoform 1
- UniProtKB: Q8TAL4 (UniProtKB/Swiss-Prot),   Q05516 (UniProtKB/Swiss-Prot),   A0A024R3C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005271715   ⟸   XM_005271658
- Peptide Label: isoform X1
- UniProtKB: Q71UL7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001341679   ⟸   NM_001354750
- Peptide Label: isoform 1
- UniProtKB: Q05516 (UniProtKB/Swiss-Prot),   Q8TAL4 (UniProtKB/Swiss-Prot),   A0A024R3C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001341680   ⟸   NM_001354751
- Peptide Label: isoform 1
- UniProtKB: Q05516 (UniProtKB/Swiss-Prot),   Q8TAL4 (UniProtKB/Swiss-Prot),   A0A024R3C6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001341681   ⟸   NM_001354752
- Peptide Label: isoform 2
- UniProtKB: A0A0S2Z4J5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000437716   ⟸   ENST00000544220
RefSeq Acc Id: ENSP00000338157   ⟸   ENST00000335953
RefSeq Acc Id: ENSP00000443013   ⟸   ENST00000535700
RefSeq Acc Id: ENSP00000376721   ⟸   ENST00000392996
RefSeq Acc Id: ENSP00000445047   ⟸   ENST00000539918
RefSeq Acc Id: ENSP00000506794   ⟸   ENST00000682278
RefSeq Acc Id: ENSP00000506894   ⟸   ENST00000682971
RefSeq Acc Id: ENSP00000508351   ⟸   ENST00000683318
RefSeq Acc Id: ENSP00000507788   ⟸   ENST00000684295
RefSeq Acc Id: ENSP00000507219   ⟸   ENST00000682810
RefSeq Acc Id: ENSP00000506953   ⟸   ENST00000683554
RefSeq Acc Id: ENSP00000506924   ⟸   ENST00000682697
RefSeq Acc Id: ENSP00000507350   ⟸   ENST00000684612
RefSeq Acc Id: ENSP00000506995   ⟸   ENST00000683233
RefSeq Acc Id: XP_047283519   ⟸   XM_047427563
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054225864   ⟸   XM_054369889
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054225865   ⟸   XM_054369890
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054225863   ⟸   XM_054369888
- Peptide Label: isoform X3
- UniProtKB: Q05516 (UniProtKB/Swiss-Prot),   Q8TAL4 (UniProtKB/Swiss-Prot),   A0A024R3C6 (UniProtKB/TrEMBL)
Protein Domains
BTB   C2H2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q05516-F1-model_v2 AlphaFold Q05516 1-673 view protein structure

Promoters
RGD ID:6789590
Promoter ID:HG_KWN:14222
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   NB4
Transcripts:ENST00000335953,   UC001POO.1
Position:
Human AssemblyChrPosition (strand)Source
Build 3611113,435,391 - 113,435,891 (+)MPROMDB
RGD ID:6789591
Promoter ID:HG_KWN:14223
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:NM_001018011
Position:
Human AssemblyChrPosition (strand)Source
Build 3611113,436,191 - 113,436,692 (+)MPROMDB
RGD ID:7222177
Promoter ID:EPDNEW_H16833
Type:initiation region
Name:ZBTB16_3
Description:zinc finger and BTB domain containing 16
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H16834  EPDNEW_H16835  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,059,403 - 114,059,463EPDNEW
RGD ID:7222175
Promoter ID:EPDNEW_H16834
Type:initiation region
Name:ZBTB16_2
Description:zinc finger and BTB domain containing 16
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H16833  EPDNEW_H16835  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,059,575 - 114,059,635EPDNEW
RGD ID:7222179
Promoter ID:EPDNEW_H16835
Type:initiation region
Name:ZBTB16_1
Description:zinc finger and BTB domain containing 16
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H16834  EPDNEW_H16833  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811114,059,714 - 114,059,774EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:12930 AgrOrtholog
COSMIC ZBTB16 COSMIC
Ensembl Genes ENSG00000109906 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000335953 ENTREZGENE
  ENST00000335953.9 UniProtKB/Swiss-Prot
  ENST00000392996 ENTREZGENE
  ENST00000392996.2 UniProtKB/Swiss-Prot
  ENST00000539918.5 UniProtKB/TrEMBL
  ENST00000544220.1 UniProtKB/TrEMBL
  ENST00000682278.1 UniProtKB/Swiss-Prot
  ENST00000682697.1 UniProtKB/Swiss-Prot
  ENST00000682810 ENTREZGENE
  ENST00000682810.1 UniProtKB/TrEMBL
  ENST00000682971.1 UniProtKB/Swiss-Prot
  ENST00000683233.1 UniProtKB/TrEMBL
  ENST00000683318 ENTREZGENE
  ENST00000683318.1 UniProtKB/Swiss-Prot
  ENST00000683554.1 UniProtKB/Swiss-Prot
  ENST00000684295 ENTREZGENE
  ENST00000684295.1 UniProtKB/Swiss-Prot
  ENST00000684612.1 UniProtKB/TrEMBL
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000109906 GTEx
HGNC ID HGNC:12930 ENTREZGENE
Human Proteome Map ZBTB16 Human Proteome Map
InterPro BTB/POZ_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SKP1/BTB/POZ_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:7704 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 7704 ENTREZGENE
OMIM 176797 OMIM
PANTHER AGAP004733-PA UniProtKB/TrEMBL
  AGAP004733-PA UniProtKB/TrEMBL
  GH18834P-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GM08392P UniProtKB/TrEMBL
  PLZFA UniProtKB/TrEMBL
  ZINC FINGER PROTEIN UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN UniProtKB/TrEMBL
  ZINC FINGER PROTEIN UniProtKB/TrEMBL
Pfam BTB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2_6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37517 PharmGKB, RGD
PROSITE BTB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART BTB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZnF_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF54695 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R3C6 ENTREZGENE, UniProtKB/TrEMBL
  A0A0S2Z4J5 ENTREZGENE, UniProtKB/TrEMBL
  A0A804HIC1_HUMAN UniProtKB/TrEMBL
  A0A804HJ45_HUMAN UniProtKB/TrEMBL
  F5H6C3_HUMAN UniProtKB/TrEMBL
  H0YGW2_HUMAN UniProtKB/TrEMBL
  Q05516 ENTREZGENE
  Q71UL7 ENTREZGENE, UniProtKB/TrEMBL
  Q8TAL4 ENTREZGENE
  ZBT16_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q8TAL4 UniProtKB/Swiss-Prot