ZBTB10 (zinc finger and BTB domain containing 10) - Rat Genome Database

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Gene: ZBTB10 (zinc finger and BTB domain containing 10) Homo sapiens
Analyze
Symbol: ZBTB10
Name: zinc finger and BTB domain containing 10
RGD ID: 1348951
HGNC Page HGNC:30953
Description: Enables telomeric DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Located in chromosome, telomeric region and nucleoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ12752; RINZF; zinc finger and BTB domain-containing protein 10; zinc finger protein RIN ZF; zinc finger protein RINZF
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: LOC100421197  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38880,485,593 - 80,526,265 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl880,485,619 - 80,526,265 (+)EnsemblGRCh38hg38GRCh38
GRCh37881,397,828 - 81,438,500 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36881,561,003 - 81,597,165 (+)NCBINCBI36Build 36hg18NCBI36
Build 34881,561,002 - 81,595,322NCBI
Celera877,403,411 - 77,439,573 (+)NCBICelera
Cytogenetic Map8q21.13NCBI
HuRef876,887,755 - 76,928,401 (+)NCBIHuRef
CHM1_1881,449,813 - 81,490,426 (+)NCBICHM1_1
T2T-CHM13v2.0880,917,153 - 80,957,852 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-demecolcine  (EXP)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
17beta-hydroxy-17-methylestra-4,9,11-trien-3-one  (EXP)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP)
2-hydroxypropanoic acid  (EXP)
6-propyl-2-thiouracil  (ISO)
aflatoxin B1  (EXP)
amitrole  (ISO)
ammonium chloride  (ISO)
antirheumatic drug  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
avobenzone  (EXP)
benzo[a]pyrene  (EXP)
bisphenol A  (EXP,ISO)
carbon nanotube  (ISO)
chromium(6+)  (EXP)
cisplatin  (EXP)
clorgyline  (EXP)
clotrimazole  (ISO)
cobalt dichloride  (ISO)
colforsin daropate hydrochloride  (EXP)
copper(II) sulfate  (EXP)
coumestrol  (EXP)
crocidolite asbestos  (EXP)
cyclosporin A  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
entinostat  (EXP)
fenvalerate  (ISO)
fluoranthene  (ISO)
folic acid  (ISO)
formaldehyde  (EXP)
FR900359  (EXP)
geraniol  (EXP)
hydrogen cyanide  (ISO)
leflunomide  (EXP)
lipopolysaccharide  (EXP,ISO)
manganese(II) chloride  (ISO)
mercury atom  (EXP)
mercury dibromide  (EXP)
mercury(0)  (EXP)
methimazole  (ISO)
methylisothiazolinone  (EXP)
methylmercury chloride  (EXP)
N-methyl-4-phenylpyridinium  (EXP)
N1'-[2-[[5-[(dimethylamino)methyl]-2-furanyl]methylthio]ethyl]-N1-methyl-2-nitroethene-1,1-diamine  (ISO)
nickel atom  (EXP)
nickel sulfate  (EXP)
orphenadrine  (ISO)
ozone  (ISO)
paracetamol  (EXP)
PCB138  (ISO)
perfluorohexanesulfonic acid  (ISO)
phenylmercury acetate  (EXP)
potassium chromate  (EXP)
potassium cyanide  (ISO)
quercetin  (EXP)
quercetin 3-O-beta-D-galactopyranoside  (EXP)
rac-lactic acid  (EXP)
ranitidine  (ISO)
resveratrol  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (EXP)
Soman  (ISO)
tetrachloromethane  (ISO)
titanium dioxide  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
troglitazone  (ISO)
tungsten  (ISO)
urethane  (EXP)
valproic acid  (EXP)
vinclozolin  (ISO)
vincristine  (EXP)
vorinostat  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Astigmatism  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:14702039   PMID:15489334   PMID:18029348   PMID:20382698   PMID:21145461   PMID:21156786   PMID:21873635   PMID:22197932   PMID:22493691   PMID:22829776   PMID:22895009   PMID:22939629  
PMID:22990118   PMID:23254909   PMID:23471840   PMID:23667531   PMID:23817569   PMID:24035498   PMID:24239288   PMID:24388013   PMID:25416956   PMID:25609649   PMID:25959826   PMID:26186194  
PMID:26496610   PMID:26549023   PMID:26972000   PMID:27234298   PMID:28514442   PMID:28786561   PMID:29117863   PMID:29229926   PMID:29395067   PMID:29467282   PMID:29507755   PMID:29509190  
PMID:29568061   PMID:29844126   PMID:29892012   PMID:30021884   PMID:30629181   PMID:30655611   PMID:30804394   PMID:31091453   PMID:31753913   PMID:32296183   PMID:33301849   PMID:33961781  
PMID:34079125   PMID:34244565   PMID:35140242   PMID:35271311   PMID:35306527   PMID:35439318   PMID:35563538   PMID:35608340   PMID:35785414   PMID:35850772   PMID:36089195   PMID:36657642  
PMID:37689310   PMID:37827155   PMID:37834257  


Genomics

Comparative Map Data
ZBTB10
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38880,485,593 - 80,526,265 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl880,485,619 - 80,526,265 (+)EnsemblGRCh38hg38GRCh38
GRCh37881,397,828 - 81,438,500 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36881,561,003 - 81,597,165 (+)NCBINCBI36Build 36hg18NCBI36
Build 34881,561,002 - 81,595,322NCBI
Celera877,403,411 - 77,439,573 (+)NCBICelera
Cytogenetic Map8q21.13NCBI
HuRef876,887,755 - 76,928,401 (+)NCBIHuRef
CHM1_1881,449,813 - 81,490,426 (+)NCBICHM1_1
T2T-CHM13v2.0880,917,153 - 80,957,852 (+)NCBIT2T-CHM13v2.0
Zbtb10
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3939,315,627 - 9,350,393 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl39,315,662 - 9,350,393 (+)EnsemblGRCm39 Ensembl
GRCm3839,250,567 - 9,285,333 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl39,250,602 - 9,285,333 (+)EnsemblGRCm38mm10GRCm38
MGSCv3739,250,567 - 9,285,333 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3639,120,847 - 9,268,406 (+)NCBIMGSCv36mm8
Celera39,264,557 - 9,301,335 (+)NCBICelera
Cytogenetic Map3A1NCBI
cM Map32.25NCBI
Zbtb10
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8294,382,670 - 94,417,308 (-)NCBIGRCr8
mRatBN7.2292,475,254 - 92,509,892 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl292,479,014 - 92,512,515 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx298,984,227 - 99,015,192 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0297,105,240 - 97,136,209 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0292,162,106 - 92,193,075 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0294,692,939 - 94,730,976 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl294,692,939 - 94,730,978 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02114,442,396 - 114,479,721 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.02113,381,190 - 113,381,601 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4294,538,617 - 94,569,036 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1294,483,578 - 94,513,998 (-)NCBI
Celera288,065,419 - 88,095,620 (-)NCBICelera
Cytogenetic Map2q23NCBI
Zbtb10
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955444983,418 - 1,006,009 (-)EnsemblChiLan1.0
ChiLan1.0NW_004955444983,308 - 1,006,439 (-)NCBIChiLan1.0ChiLan1.0
ZBTB10
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2796,226,434 - 96,284,808 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1871,852,783 - 71,912,643 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0877,011,325 - 77,051,778 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1878,635,797 - 78,676,593 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl878,636,444 - 78,669,851 (+)Ensemblpanpan1.1panPan2
ZBTB10
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12927,750,151 - 27,781,995 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2927,750,146 - 27,777,650 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2928,023,919 - 28,056,757 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02927,874,508 - 27,907,339 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2927,873,837 - 28,056,534 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12927,928,249 - 27,961,065 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02927,958,623 - 27,991,433 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02928,315,753 - 28,348,605 (+)NCBIUU_Cfam_GSD_1.0
Zbtb10
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440530351,323,733 - 51,361,838 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366563,519,033 - 3,550,862 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366563,516,756 - 3,552,278 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZBTB10
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl456,136,033 - 56,175,296 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1456,138,082 - 56,174,337 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2461,268,500 - 61,304,770 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ZBTB10
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1875,918,402 - 75,959,221 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl875,919,657 - 75,952,485 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603965,234,924 - 65,276,024 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Zbtb10
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462474410,878,616 - 10,916,852 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462474410,874,076 - 10,917,976 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZBTB10
43 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8q21.11-21.13(chr8:73519300-82655582)x1 copy number loss See cases [RCV000051117] Chr8:73519300..82655582 [GRCh38]
Chr8:74431535..83567817 [GRCh37]
Chr8:74594089..83730372 [NCBI36]
Chr8:8q21.11-21.13		 pathogenic
GRCh38/hg38 8q12.3-21.13(chr8:61691800-82537696)x3 copy number gain See cases [RCV000053654] Chr8:61691800..82537696 [GRCh38]
Chr8:62604359..83449931 [GRCh37]
Chr8:62766913..83612486 [NCBI36]
Chr8:8q12.3-21.13		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8q21.11-21.2(chr8:73879385-85611466)x1 copy number loss See cases [RCV000054259] Chr8:73879385..85611466 [GRCh38]
Chr8:74791620..86523695 [GRCh37]
Chr8:74954174..86710947 [NCBI36]
Chr8:8q21.11-21.2		 pathogenic
GRCh38/hg38 8q21.13-21.3(chr8:77765431-91839285)x1 copy number loss See cases [RCV000054261] Chr8:77765431..91839285 [GRCh38]
Chr8:78677666..92851513 [GRCh37]
Chr8:78840221..92920689 [NCBI36]
Chr8:8q21.13-21.3		 pathogenic
GRCh38/hg38 8q21.13-22.1(chr8:78672463-95366868)x1 copy number loss See cases [RCV000054262] Chr8:78672463..95366868 [GRCh38]
Chr8:79584698..96379096 [GRCh37]
Chr8:79747253..96448272 [NCBI36]
Chr8:8q21.13-22.1		 pathogenic
GRCh38/hg38 8q21.13(chr8:74905308-81339951)x1 copy number loss See cases [RCV000133719] Chr8:74905308..81339951 [GRCh38]
Chr8:75817543..82252186 [GRCh37]
Chr8:75980098..82414741 [NCBI36]
Chr8:8q21.13		 pathogenic
GRCh38/hg38 8q13.1-22.1(chr8:66171669-93505509)x3 copy number gain See cases [RCV000137050] Chr8:66171669..93505509 [GRCh38]
Chr8:67083904..94517737 [GRCh37]
Chr8:67246458..94586913 [NCBI36]
Chr8:8q13.1-22.1		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3		 pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3 copy number gain See cases [RCV000139539] Chr8:46031340..139285494 [GRCh38]
Chr8:46942962..140297737 [GRCh37]
Chr8:47062127..140366919 [NCBI36]
Chr8:8q11.1-24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q13.3-21.13(chr8:70971013-82019151)x3 copy number gain See cases [RCV000240367] Chr8:70971013..82019151 [GRCh37]
Chr8:8q13.3-21.13		 likely pathogenic
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3 copy number gain not provided [RCV000848192] Chr8:31936551..146295771 [GRCh37]
Chr8:8p12-q24.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.11-21.13(chr8:75197438-81685526)x1 copy number loss See cases [RCV000445718] Chr8:75197438..81685526 [GRCh37]
Chr8:8q21.11-21.13		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.11-21.13(chr8:77751515-83516216)x1 copy number loss See cases [RCV000511429] Chr8:77751515..83516216 [GRCh37]
Chr8:8q21.11-21.13		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.13(chr8:80883771-81650440)x3 copy number gain See cases [RCV000511010] Chr8:80883771..81650440 [GRCh37]
Chr8:8q21.13		 likely benign
NM_001105539.3(ZBTB10):c.145C>T (p.Pro49Ser) single nucleotide variant Inborn genetic diseases [RCV003282131] Chr8:80486955 [GRCh38]
Chr8:81399190 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.473C>A (p.Pro158Gln) single nucleotide variant Inborn genetic diseases [RCV003299217] Chr8:80487283 [GRCh38]
Chr8:81399518 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.524A>C (p.Gln175Pro) single nucleotide variant Inborn genetic diseases [RCV003255882] Chr8:80487334 [GRCh38]
Chr8:81399569 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.757T>G (p.Ser253Ala) single nucleotide variant Inborn genetic diseases [RCV003276310] Chr8:80487567 [GRCh38]
Chr8:81399802 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
NM_001105539.3(ZBTB10):c.5_7del (p.Ser2del) deletion not provided [RCV001649226] Chr8:80486813..80486815 [GRCh38]
Chr8:81399048..81399050 [GRCh37]
Chr8:8q21.13		 benign
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
NM_001105539.3(ZBTB10):c.182G>T (p.Arg61Leu) single nucleotide variant Inborn genetic diseases [RCV003240101] Chr8:80486992 [GRCh38]
Chr8:81399227 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.859C>T (p.Leu287Phe) single nucleotide variant Inborn genetic diseases [RCV003251429] Chr8:80487669 [GRCh38]
Chr8:81399904 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.478A>G (p.Thr160Ala) single nucleotide variant Inborn genetic diseases [RCV003276309] Chr8:80487288 [GRCh38]
Chr8:81399523 [GRCh37]
Chr8:8q21.13		 likely benign
NM_001105539.3(ZBTB10):c.80C>T (p.Thr27Met) single nucleotide variant Inborn genetic diseases [RCV003276311] Chr8:80486890 [GRCh38]
Chr8:81399125 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771) copy number gain Polydactyly [RCV002280629] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8q21.11-21.13(chr8:75197438-81685526) copy number loss not specified [RCV002053774] Chr8:75197438..81685526 [GRCh37]
Chr8:8q21.11-21.13		 pathogenic
GRCh37/hg19 8q21.11-21.3(chr8:77906471-88917707) copy number loss not specified [RCV002053776] Chr8:77906471..88917707 [GRCh37]
Chr8:8q21.11-21.3		 pathogenic
GRCh37/hg19 8q13.2-24.3(chr8:70382990-146295771) copy number gain not specified [RCV002053772] Chr8:70382990..146295771 [GRCh37]
Chr8:8q13.2-24.3		 pathogenic
NM_001105539.3(ZBTB10):c.466C>T (p.Arg156Ter) single nucleotide variant Astigmatism [RCV002245528] Chr8:80487276 [GRCh38]
Chr8:81399511 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8q21.11-21.3(chr8:75904944-87097083)x1 copy number loss Chromosome 8q21.11 deletion syndrome [RCV002279750] Chr8:75904944..87097083 [GRCh37]
Chr8:8q21.11-21.3		 pathogenic
GRCh37/hg19 8q13.2-24.3(chr8:68912432-146295771)x2 copy number gain See cases [RCV002292707] Chr8:68912432..146295771 [GRCh37]
Chr8:8q13.2-24.3		 pathogenic
NM_001105539.3(ZBTB10):c.486T>G (p.Asp162Glu) single nucleotide variant Inborn genetic diseases [RCV003255881] Chr8:80487296 [GRCh38]
Chr8:81399531 [GRCh37]
Chr8:8q21.13		 likely benign
NM_001105539.3(ZBTB10):c.77C>T (p.Ser26Phe) single nucleotide variant Inborn genetic diseases [RCV003260881] Chr8:80486887 [GRCh38]
Chr8:81399122 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8q21.12-21.13(chr8:79876744-83112711)x3 copy number gain not provided [RCV002472757] Chr8:79876744..83112711 [GRCh37]
Chr8:8q21.12-21.13		 uncertain significance
GRCh37/hg19 8q21.12-24.11(chr8:79409349-119040631)x3 copy number gain not provided [RCV002474526] Chr8:79409349..119040631 [GRCh37]
Chr8:8q21.12-24.11		 pathogenic
NM_001105539.3(ZBTB10):c.1566T>G (p.Asn522Lys) single nucleotide variant Inborn genetic diseases [RCV002901048] Chr8:80500087 [GRCh38]
Chr8:81412322 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.961G>A (p.Ala321Thr) single nucleotide variant Inborn genetic diseases [RCV002864670] Chr8:80487771 [GRCh38]
Chr8:81400006 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.1643A>G (p.Glu548Gly) single nucleotide variant Inborn genetic diseases [RCV002997413] Chr8:80500164 [GRCh38]
Chr8:81412399 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.233A>T (p.Glu78Val) single nucleotide variant Inborn genetic diseases [RCV002733135] Chr8:80487043 [GRCh38]
Chr8:81399278 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.1715G>T (p.Gly572Val) single nucleotide variant Inborn genetic diseases [RCV002992875] Chr8:80500236 [GRCh38]
Chr8:81412471 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.90C>A (p.Asn30Lys) single nucleotide variant Inborn genetic diseases [RCV002686736] Chr8:80486900 [GRCh38]
Chr8:81399135 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.346G>C (p.Ala116Pro) single nucleotide variant Inborn genetic diseases [RCV002952023] Chr8:80487156 [GRCh38]
Chr8:81399391 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.590G>A (p.Ser197Asn) single nucleotide variant Inborn genetic diseases [RCV002977816] Chr8:80487400 [GRCh38]
Chr8:81399635 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.2556T>A (p.Asp852Glu) single nucleotide variant Inborn genetic diseases [RCV002644699] Chr8:80519468 [GRCh38]
Chr8:81431703 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.704C>T (p.Pro235Leu) single nucleotide variant Inborn genetic diseases [RCV002763409] Chr8:80487514 [GRCh38]
Chr8:81399749 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.322G>A (p.Gly108Ser) single nucleotide variant Inborn genetic diseases [RCV002666051] Chr8:80487132 [GRCh38]
Chr8:81399367 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.149C>T (p.Pro50Leu) single nucleotide variant Inborn genetic diseases [RCV002742356] Chr8:80486959 [GRCh38]
Chr8:81399194 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.239C>T (p.Ser80Phe) single nucleotide variant Inborn genetic diseases [RCV002963575] Chr8:80487049 [GRCh38]
Chr8:81399284 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.86A>G (p.Asn29Ser) single nucleotide variant Inborn genetic diseases [RCV002679016] Chr8:80486896 [GRCh38]
Chr8:81399131 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.79A>G (p.Thr27Ala) single nucleotide variant Inborn genetic diseases [RCV003255883] Chr8:80486889 [GRCh38]
Chr8:81399124 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.461A>G (p.Asn154Ser) single nucleotide variant Inborn genetic diseases [RCV003297175] Chr8:80487271 [GRCh38]
Chr8:81399506 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.1876C>G (p.Leu626Val) single nucleotide variant Inborn genetic diseases [RCV003190132] Chr8:80513924 [GRCh38]
Chr8:81426159 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.217G>A (p.Glu73Lys) single nucleotide variant Inborn genetic diseases [RCV003194991] Chr8:80487027 [GRCh38]
Chr8:81399262 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.2054A>C (p.Tyr685Ser) single nucleotide variant Inborn genetic diseases [RCV003341135] Chr8:80518496 [GRCh38]
Chr8:81430731 [GRCh37]
Chr8:8q21.13		 uncertain significance
NM_001105539.3(ZBTB10):c.1886G>A (p.Gly629Glu) single nucleotide variant Inborn genetic diseases [RCV003371717] Chr8:80513934 [GRCh38]
Chr8:81426169 [GRCh37]
Chr8:8q21.13		 uncertain significance
GRCh37/hg19 8q21.12-22.3(chr8:79046933-102008860)x3 copy number gain not provided [RCV003484742] Chr8:79046933..102008860 [GRCh37]
Chr8:8q21.12-22.3		 pathogenic
GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3 copy number gain not specified [RCV003986754] Chr8:27024288..89410121 [GRCh37]
Chr8:8p21.2-q21.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not specified [RCV003986742] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR27Ahsa-miR-27a-3pMirtarbaseexternal_infoWestern blot//Luciferase reporter assay//Reporter Functional MTI18006846
MIR27Ahsa-miR-27a-3pMirtarbaseexternal_infoReporter assayFunctional MTI20382698
MIR27Ahsa-miR-27a-3pTarbaseexternal_infoReporter GenePOSITIVE

Predicted Target Of
Summary Value
Count of predictions:4142
Count of miRNA genes:940
Interacting mature miRNAs:1185
Transcripts:ENST00000379091, ENST00000426744, ENST00000430430, ENST00000455036
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
RH11916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37881,438,230 - 81,438,329UniSTSGRCh37
Build 36881,600,785 - 81,600,884RGDNCBI36
Celera877,443,193 - 77,443,292RGD
Cytogenetic Map8q13-q21.1UniSTS
HuRef876,928,131 - 76,928,230UniSTS
GeneMap99-GB4 RH Map8404.21UniSTS
NCBI RH Map8870.0UniSTS
RH102223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37881,397,899 - 81,398,058UniSTSGRCh37
Build 36881,560,454 - 81,560,613RGDNCBI36
Celera877,402,862 - 77,403,021RGD
Cytogenetic Map8q13-q21.1UniSTS
HuRef876,887,800 - 76,887,959UniSTS
GeneMap99-GB4 RH Map8404.21UniSTS
RH120455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37881,427,370 - 81,427,696UniSTSGRCh37
Build 36881,589,925 - 81,590,251RGDNCBI36
Celera877,432,333 - 77,432,659RGD
Cytogenetic Map8q13-q21.1UniSTS
HuRef876,917,271 - 76,917,597UniSTS
TNG Radiation Hybrid Map839930.0UniSTS
RH78774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37881,436,019 - 81,436,146UniSTSGRCh37
Build 36881,598,574 - 81,598,701RGDNCBI36
Celera877,440,982 - 77,441,109RGD
Cytogenetic Map8q13-q21.1UniSTS
HuRef876,925,920 - 76,926,047UniSTS
GeneMap99-GB4 RH Map8401.78UniSTS
RH68928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37881,397,851 - 81,398,061UniSTSGRCh37
Build 36881,560,406 - 81,560,616RGDNCBI36
Celera877,402,814 - 77,403,024RGD
Cytogenetic Map8q13-q21.1UniSTS
HuRef876,887,752 - 76,887,962UniSTS
GeneMap99-GB4 RH Map8403.68UniSTS
NCBI RH Map8868.6UniSTS
ZBTB10__4922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37881,432,381 - 81,432,952UniSTSGRCh37
Build 36881,594,936 - 81,595,507RGDNCBI36
Celera877,437,344 - 77,437,915RGD
HuRef876,922,282 - 76,922,853UniSTS


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 237 1150 266 79 258 74 1356 177 741 152 815 550 9 307 965 4
Low 2177 1420 1458 544 1262 391 2996 2017 2973 264 641 1061 162 1 897 1823 1 1
Below cutoff 13 419 1 423 3 1 17 3 3 1 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001105539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001277145 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_023929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC009812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI627858 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ319673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ507398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK022814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC050061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC127097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC127098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC148254 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA865977 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OP794611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000379091   ⟹   ENSP00000368384
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl880,485,619 - 80,519,804 (+)Ensembl
RefSeq Acc Id: ENST00000426744   ⟹   ENSP00000416134
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl880,486,213 - 80,526,264 (+)Ensembl
RefSeq Acc Id: ENST00000430430   ⟹   ENSP00000387462
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl880,485,667 - 80,526,265 (+)Ensembl
RefSeq Acc Id: ENST00000455036   ⟹   ENSP00000412036
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl880,486,226 - 80,526,265 (+)Ensembl
RefSeq Acc Id: ENST00000610895   ⟹   ENSP00000484716
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl880,486,307 - 80,520,135 (+)Ensembl
RefSeq Acc Id: NM_001105539   ⟹   NP_001099009
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38880,486,226 - 80,526,265 (+)NCBI
GRCh37881,397,854 - 81,438,500 (+)NCBI
Build 36881,561,003 - 81,597,165 (+)NCBI Archive
Celera877,403,411 - 77,439,573 (+)RGD
HuRef876,887,755 - 76,928,401 (+)NCBI
CHM1_1881,450,374 - 81,490,426 (+)NCBI
T2T-CHM13v2.0880,917,786 - 80,957,852 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001277145   ⟹   NP_001264074
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38880,485,593 - 80,526,265 (+)NCBI
HuRef876,887,755 - 76,928,401 (+)NCBI
CHM1_1881,449,813 - 81,490,426 (+)NCBI
T2T-CHM13v2.0880,917,153 - 80,957,852 (+)NCBI
Sequence:
RefSeq Acc Id: NM_023929   ⟹   NP_076418
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38880,486,226 - 80,526,265 (+)NCBI
GRCh37881,397,854 - 81,438,500 (+)NCBI
Build 36881,561,003 - 81,597,165 (+)NCBI Archive
Celera877,403,411 - 77,439,573 (+)RGD
HuRef876,887,755 - 76,928,401 (+)NCBI
CHM1_1881,450,374 - 81,490,426 (+)NCBI
T2T-CHM13v2.0880,917,786 - 80,957,852 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_076418   ⟸   NM_023929
- Peptide Label: isoform b
- UniProtKB: Q96DT7 (UniProtKB/Swiss-Prot),   Q9H9H3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001099009   ⟸   NM_001105539
- Peptide Label: isoform a
- UniProtKB: Q8IXI9 (UniProtKB/Swiss-Prot),   Q86W96 (UniProtKB/Swiss-Prot),   A4FVD0 (UniProtKB/Swiss-Prot),   Q96MH9 (UniProtKB/Swiss-Prot),   Q96DT7 (UniProtKB/Swiss-Prot),   A8E4L4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001264074   ⟸   NM_001277145
- Peptide Label: isoform c
- UniProtKB: Q96DT7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000416134   ⟸   ENST00000426744
RefSeq Acc Id: ENSP00000484716   ⟸   ENST00000610895
RefSeq Acc Id: ENSP00000412036   ⟸   ENST00000455036
RefSeq Acc Id: ENSP00000368384   ⟸   ENST00000379091
RefSeq Acc Id: ENSP00000387462   ⟸   ENST00000430430
Protein Domains
BTB   C2H2-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96DT7-F1-model_v2 AlphaFold Q96DT7 1-871 view protein structure

Promoters
RGD ID:6807168
Promoter ID:HG_KWN:61581
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000379085,   NM_001105539,   NM_023929,   OTTHUMT00000338055,   UC003YBV.2,   UC010LZT.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36881,560,336 - 81,562,372 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30953 AgrOrtholog
COSMIC ZBTB10 COSMIC
Ensembl Genes ENSG00000205189 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000379091 ENTREZGENE
  ENST00000379091.8 UniProtKB/Swiss-Prot
  ENST00000426744 ENTREZGENE
  ENST00000426744.5 UniProtKB/Swiss-Prot
  ENST00000430430.5 UniProtKB/Swiss-Prot
  ENST00000455036 ENTREZGENE
  ENST00000455036.8 UniProtKB/Swiss-Prot
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000205189 GTEx
HGNC ID HGNC:30953 ENTREZGENE
Human Proteome Map ZBTB10 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:65986 UniProtKB/Swiss-Prot
NCBI Gene 65986 ENTREZGENE
OMIM 618576 OMIM
PANTHER AGAP004733-PA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC FINGER AND BTB DOMAIN CONTAINING 10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam BTB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/TrEMBL
PharmGKB PA134883318 PharmGKB
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 A4FVD0 ENTREZGENE
  A8E4L4 ENTREZGENE, UniProtKB/TrEMBL
  Q86W96 ENTREZGENE
  Q8IXI9 ENTREZGENE
  Q96DT7 ENTREZGENE
  Q96MH9 ENTREZGENE
  Q9H9H3 ENTREZGENE, UniProtKB/TrEMBL
  ZBT10_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A4FVD0 UniProtKB/Swiss-Prot
  Q86W96 UniProtKB/Swiss-Prot
  Q8IXI9 UniProtKB/Swiss-Prot
  Q96MH9 UniProtKB/Swiss-Prot