ZBTB8B (zinc finger and BTB domain containing 8B) - Rat Genome Database

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Gene: ZBTB8B (zinc finger and BTB domain containing 8B) Homo sapiens
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Symbol: ZBTB8B
Name: zinc finger and BTB domain containing 8B
RGD ID: 2307066
HGNC Page HGNC:37057
Description: Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DKFZp547H154; putative zinc finger and BTB domain-containing protein 8B; RP1-27O5.1; zinc finger and BTB domain-containing protein 8B; ZNF916B
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Black 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
GRCh38132,465,072 - 32,496,686 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl132,465,050 - 32,496,686 (+)Ensemblhg38GRCh38
GRCh37132,930,673 - 32,962,287 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36132,694,834 - 32,726,047 (+)NCBIBuild 36Build 36hg18NCBI36
Celera131,198,480 - 31,221,280 (+)NCBICelera
Cytogenetic Map1p35.1NCBI
HuRef131,046,019 - 31,068,729 (+)NCBIHuRef
CHM1_1133,046,109 - 33,068,992 (+)NCBICHM1_1
T2T-CHM13v2.0132,322,988 - 32,354,613 (+)NCBIT2T-CHM13v2.0
JBrowse:




Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
chromatin  (ISA)
cytosol  (IDA)
nucleoplasm  (IDA)
nucleus  (IBA,IEA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:14702039   PMID:15761153   PMID:16189514   PMID:16710414   PMID:21873635   PMID:22939629   PMID:32296183   PMID:33961781   PMID:36724073  


Genomics

Comparative Map Data
ZBTB8B
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38132,465,072 - 32,496,686 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl132,465,050 - 32,496,686 (+)Ensemblhg38GRCh38
GRCh37132,930,673 - 32,962,287 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36132,694,834 - 32,726,047 (+)NCBIBuild 36Build 36hg18NCBI36
Celera131,198,480 - 31,221,280 (+)NCBICelera
Cytogenetic Map1p35.1NCBI
HuRef131,046,019 - 31,068,729 (+)NCBIHuRef
CHM1_1133,046,109 - 33,068,992 (+)NCBICHM1_1
T2T-CHM13v2.0132,322,988 - 32,354,613 (+)NCBIT2T-CHM13v2.0
Zbtb8b
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394129,320,063 - 129,340,761 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl4129,319,558 - 129,334,646 (-)EnsemblGRCm39 EnsemblGRCm39
GRCm384129,425,765 - 129,446,969 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4129,425,765 - 129,440,853 (-)Ensemblmm10GRCm38
MGSCv374129,103,009 - 129,118,062 (-)NCBIMGSCv37MGSCv37mm9NCBIm37
MGSCv364128,928,574 - 128,943,095 (-)NCBIMGSCv36mm8
Celera4127,766,845 - 127,781,898 (-)NCBICelera
Cytogenetic Map4D2.2NCBI
cM Map463.26NCBI
Zbtb8b
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85147,046,150 - 147,065,961 (-)NCBIGRCr8GRCr8GRCr8
GRCr8 Ensembl5147,050,650 - 147,066,133 (-)EnsemblGRCr8
mRatBN7.25141,765,925 - 141,781,619 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5141,766,309 - 141,781,600 (-)EnsemblmRatBN7.2
UTH_Rnor_SHR_Utx5144,466,054 - 144,472,807 (-)NCBIUTH_Rnor_SHR_UtxUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05146,235,873 - 146,242,626 (-)NCBIUTH_Rnor_SHRSP_BbbUtx_1.0UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05146,234,527 - 146,241,302 (-)NCBIUTH_Rnor_WKY_Bbb_1.0UTH_Rnor_WKY_Bbb_1.0
Rnor_6.05147,628,566 - 147,644,209 (-)NCBIRnor_6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5147,628,899 - 147,635,789 (-)Ensemblrn6Rnor6.0
Rnor_5.05151,347,880 - 151,363,202 (-)NCBIRnor_5.0Rnor_5.0rn5
RGSC_v3.45148,583,356 - 148,590,246 (-)NCBIRGSC_v3.4RGSC_v3.4rn4
Celera5140,243,083 - 140,249,853 (-)NCBICelera
Cytogenetic Map5q36NCBI
Zbtb8b
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545210,788,498 - 10,816,287 (+)Ensembl
ChiLan1.0NW_00495545210,788,487 - 10,816,287 (+)NCBIChiLan1.0ChiLan1.0
ZBTB8B
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21194,323,801 - 194,357,538 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11193,445,940 - 193,479,665 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0131,754,980 - 31,778,720 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1132,924,328 - 32,946,825 (+)NCBIPanPan1.1PanPan1.1panPan2
PanPan1.1 Ensembl132,924,328 - 32,946,803 (+)EnsemblpanPan2panpan1.1
ZBTB8B
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1268,805,482 - 68,832,415 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha265,388,890 - 65,412,746 (-)NCBIDog10K_Boxer_TashaDog10K_Boxer_Tasha
ROS_Cfam_1.0269,374,578 - 69,398,456 (-)NCBIROS_Cfam_1.0ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl269,374,750 - 69,398,467 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1266,183,529 - 66,235,434 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0267,206,880 - 67,230,408 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0268,205,954 - 68,229,496 (-)NCBIUU_Cfam_GSD_1.0UU_Cfam_GSD_1.0
Zbtb8b
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505849,610,980 - 49,632,562 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647415,441,862 - 15,456,683 (+)EnsemblSpeTri2.0 Ensembl
SpeTri2.0NW_00493647415,444,209 - 15,456,846 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZBTB8B
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl688,856,238 - 88,878,113 (+)EnsemblsusScr11Sscrofa11.1
Sscrofa11.1688,856,313 - 88,878,386 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2682,825,621 - 82,921,391 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ZBTB8B
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.120100,389,497 - 100,414,867 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl20100,389,583 - 100,405,616 (-)EnsemblChlSab1.1 EnsemblchlSab2Vervet-AGM
Vero_WHO_p1.0NW_02366603316,273,917 - 16,299,903 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Zbtb8b
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476415,663,901 - 15,681,990 (+)EnsemblHetGla_female_1.0 EnsemblhetGla2HetGla_female_1.0 Ensembl
HetGla 1.0NW_00462476415,663,879 - 15,683,646 (+)NCBIHetGla 1.0HetGla 1.0hetGla2
Zbtb8b
(Rattus rattus - black rat)
Black Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rrattus_CSIRO_v1128,710,629 - 28,726,379 (+)NCBIRrattus_CSIRO_v1

Variants

.
Variants in ZBTB8B
43 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p35.2-35.1(chr1:30766758-33359428)x1 copy number loss See cases [RCV000053802] Chr1:30766758..33359428 [GRCh38]
Chr1:31239605..33825029 [GRCh37]
Chr1:31012192..33597616 [NCBI36]
Chr1:1p35.2-35.1		 pathogenic
GRCh38/hg38 1p35.3-35.1(chr1:28424867-33122854)x1 copy number loss See cases [RCV000135447] Chr1:28424867..33122854 [GRCh38]
Chr1:28751378..33588455 [GRCh37]
Chr1:28623965..33361042 [NCBI36]
Chr1:1p35.3-35.1		 pathogenic
GRCh38/hg38 1p36.11-34.2(chr1:24381206-41401517)x3 copy number gain See cases [RCV000138891] Chr1:24381206..41401517 [GRCh38]
Chr1:24707696..41886350 [GRCh37]
Chr1:24580283..41658937 [NCBI36]
Chr1:1p36.11-34.2		 pathogenic
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12		 likely benign
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p35.1(chr1:32608682-32953541)x3 copy number gain not provided [RCV000684559] Chr1:32608682..32953541 [GRCh37]
Chr1:1p35.1		 uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p35.2-34.3(chr1:31562164-37421958)x3 copy number gain not provided [RCV000748949] Chr1:31562164..37421958 [GRCh37]
Chr1:1p35.2-34.3		 pathogenic
NM_001145720.2(ZBTB8B):c.109G>A (p.Ala37Thr) single nucleotide variant not specified [RCV004317859] Chr1:32470733 [GRCh38]
Chr1:32936334 [GRCh37]
Chr1:1p35.1		 uncertain significance
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1		 uncertain significance
GRCh37/hg19 1p35.1-34.3(chr1:32859415-36454915) copy number loss not provided [RCV000767772] Chr1:32859415..36454915 [GRCh37]
Chr1:1p35.1-34.3		 pathogenic
GRCh37/hg19 1p35.2-35.1(chr1:32139063-32940848)x4 copy number gain not provided [RCV000846712] Chr1:32139063..32940848 [GRCh37]
Chr1:1p35.2-35.1		 uncertain significance
GRCh37/hg19 1p35.2-35.1(chr1:30819875-34380419)x3 copy number gain not provided [RCV001005079] Chr1:30819875..34380419 [GRCh37]
Chr1:1p35.2-35.1		 likely pathogenic
NM_001145720.2(ZBTB8B):c.500G>T (p.Gly167Val) single nucleotide variant not specified [RCV004326523] Chr1:32471124 [GRCh38]
Chr1:32936725 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.772G>A (p.Val258Met) single nucleotide variant not specified [RCV004295665] Chr1:32471396 [GRCh38]
Chr1:32936997 [GRCh37]
Chr1:1p35.1		 likely benign
GRCh37/hg19 1p35.1(chr1:32925002-33084424)x1 copy number loss not provided [RCV001832937] Chr1:32925002..33084424 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1484C>T (p.Thr495Met) single nucleotide variant not specified [RCV004233134] Chr1:32485414 [GRCh38]
Chr1:32951015 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.679A>G (p.Ile227Val) single nucleotide variant not specified [RCV004194331] Chr1:32471303 [GRCh38]
Chr1:32936904 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1255G>A (p.Gly419Arg) single nucleotide variant not specified [RCV004137816] Chr1:32485185 [GRCh38]
Chr1:32950786 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1313T>G (p.Met438Arg) single nucleotide variant not specified [RCV004242783] Chr1:32485243 [GRCh38]
Chr1:32950844 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.677G>C (p.Arg226Pro) single nucleotide variant not specified [RCV004199617] Chr1:32471301 [GRCh38]
Chr1:32936902 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.542A>T (p.Glu181Val) single nucleotide variant not specified [RCV004152563] Chr1:32471166 [GRCh38]
Chr1:32936767 [GRCh37]
Chr1:1p35.1		 likely benign
NM_001145720.2(ZBTB8B):c.880G>A (p.Asp294Asn) single nucleotide variant not specified [RCV004211607] Chr1:32471504 [GRCh38]
Chr1:32937105 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.812C>T (p.Ala271Val) single nucleotide variant not specified [RCV004164611] Chr1:32471436 [GRCh38]
Chr1:32937037 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1358A>G (p.Glu453Gly) single nucleotide variant not specified [RCV004101987] Chr1:32485288 [GRCh38]
Chr1:32950889 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1081C>T (p.Arg361Cys) single nucleotide variant not specified [RCV004170293] Chr1:32480980 [GRCh38]
Chr1:32946581 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.953T>A (p.Met318Lys) single nucleotide variant not specified [RCV004150293] Chr1:32471577 [GRCh38]
Chr1:32937178 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.984G>C (p.Glu328Asp) single nucleotide variant not specified [RCV004150294] Chr1:32471608 [GRCh38]
Chr1:32937209 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.472A>T (p.Ser158Cys) single nucleotide variant not specified [RCV004155196] Chr1:32471096 [GRCh38]
Chr1:32936697 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.755C>T (p.Pro252Leu) single nucleotide variant not specified [RCV004173127] Chr1:32471379 [GRCh38]
Chr1:32936980 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1414G>A (p.Asp472Asn) single nucleotide variant not specified [RCV004196388] Chr1:32485344 [GRCh38]
Chr1:32950945 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1223C>T (p.Thr408Met) single nucleotide variant not specified [RCV004094367] Chr1:32485153 [GRCh38]
Chr1:32950754 [GRCh37]
Chr1:1p35.1		 uncertain significance
GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3 copy number gain Trisomy 12p [RCV003447845] Chr1:99125..34026935 [GRCh38]
Chr1:1p36.33-35.1		 pathogenic
NM_001145720.2(ZBTB8B):c.965A>G (p.Gln322Arg) single nucleotide variant not specified [RCV004688998] Chr1:32471589 [GRCh38]
Chr1:32937190 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.319A>G (p.Met107Val) single nucleotide variant not specified [RCV004688996] Chr1:32470943 [GRCh38]
Chr1:32936544 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1472G>A (p.Arg491Gln) single nucleotide variant not specified [RCV004688997] Chr1:32485402 [GRCh38]
Chr1:32951003 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.270G>C (p.Leu90Phe) single nucleotide variant not specified [RCV004884979] Chr1:32470894 [GRCh38]
Chr1:32936495 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1076A>G (p.His359Arg) single nucleotide variant not specified [RCV004884978] Chr1:32480975 [GRCh38]
Chr1:32946576 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.698T>C (p.Phe233Ser) single nucleotide variant not specified [RCV004884980] Chr1:32471322 [GRCh38]
Chr1:32936923 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.697T>A (p.Phe233Ile) single nucleotide variant not specified [RCV004884984] Chr1:32471321 [GRCh38]
Chr1:32936922 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.671C>A (p.Pro224His) single nucleotide variant not specified [RCV004884983] Chr1:32471295 [GRCh38]
Chr1:32936896 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1139G>A (p.Arg380Gln) single nucleotide variant not specified [RCV004893074] Chr1:32481038 [GRCh38]
Chr1:32946639 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.667C>G (p.Pro223Ala) single nucleotide variant not specified [RCV004893075] Chr1:32471291 [GRCh38]
Chr1:32936892 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1246C>T (p.Arg416Trp) single nucleotide variant not specified [RCV005297339] Chr1:32485176 [GRCh38]
Chr1:32950777 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.984G>T (p.Glu328Asp) single nucleotide variant not specified [RCV005313600] Chr1:32471608 [GRCh38]
Chr1:32937209 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.16T>G (p.Tyr6Asp) single nucleotide variant not specified [RCV005297342] Chr1:32470640 [GRCh38]
Chr1:32936241 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1339G>C (p.Ala447Pro) single nucleotide variant not specified [RCV005297338] Chr1:32485269 [GRCh38]
Chr1:32950870 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.502A>T (p.Thr168Ser) single nucleotide variant not specified [RCV005297340] Chr1:32471126 [GRCh38]
Chr1:32936727 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.167A>G (p.Tyr56Cys) single nucleotide variant not specified [RCV005297341] Chr1:32470791 [GRCh38]
Chr1:32936392 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.869C>T (p.Ala290Val) single nucleotide variant not specified [RCV004893077] Chr1:32471493 [GRCh38]
Chr1:32937094 [GRCh37]
Chr1:1p35.1		 likely benign
NM_001145720.2(ZBTB8B):c.1082G>A (p.Arg361His) single nucleotide variant not specified [RCV004343714] Chr1:32480981 [GRCh38]
Chr1:32946582 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1186C>T (p.Arg396Cys) single nucleotide variant not specified [RCV004481152] Chr1:32485116 [GRCh38]
Chr1:32950717 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.1340C>A (p.Ala447Asp) single nucleotide variant not specified [RCV004481153] Chr1:32485270 [GRCh38]
Chr1:32950871 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.236T>C (p.Ile79Thr) single nucleotide variant not specified [RCV004481154] Chr1:32470860 [GRCh38]
Chr1:32936461 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.551A>G (p.Lys184Arg) single nucleotide variant not specified [RCV004481156] Chr1:32471175 [GRCh38]
Chr1:32936776 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.619G>T (p.Val207Leu) single nucleotide variant not specified [RCV004884981] Chr1:32471243 [GRCh38]
Chr1:32936844 [GRCh37]
Chr1:1p35.1		 uncertain significance
NM_001145720.2(ZBTB8B):c.200C>A (p.Ser67Tyr) single nucleotide variant not specified [RCV004893076] Chr1:32470824 [GRCh38]
Chr1:32936425 [GRCh37]
Chr1:1p35.1		 uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:4010
Count of miRNA genes:1223
Interacting mature miRNAs:1526
Transcripts:ENST00000609129
Prediction methods:Miranda
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1576329MYI9_HMyocardial infarction susceptibility QTL 9 (human)12Myocardial infarction susceptibilityearly-onset1758550333585503Human
407004266GWAS653242_Hinterleukin 2 measurement QTL GWAS653242 (human)0.000009interleukin 2 measurement13246917632469177Human
597021838GWAS1117912_Hinterleukin 2 measurement QTL GWAS1117912 (human)0.000009blood interleukin-2 amount (VT:0008598)13246917632469177Human
1576325MYI1_HMyocardial infarction susceptibility QTL 1 (human)11.681e-12Myocardial infarction susceptibilityearly-onset1758550333585503Human
1643380BW316_HBody weight QTL 316 (human)2.620.0002Body weightBMI1758550333585503Human

Markers in Region
D10S16   No map positions available.
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1096 2285 2519 2023 4852 1452 2014 4 376 1161 223 2116 5689 5322 52 3705 695 1704 1525 165

Sequence


Ensembl Acc Id: ENST00000609129   ⟹   ENSP00000476499
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl132,465,072 - 32,496,686 (+)Ensembl
Ensembl Acc Id: ENST00000930949   ⟹   ENSP00000601008
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl132,465,050 - 32,488,707 (+)Ensembl
Ensembl Acc Id: ENST00000930950   ⟹   ENSP00000601009
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl132,465,111 - 32,487,069 (+)Ensembl
Ensembl Acc Id: ENST00000930951   ⟹   ENSP00000601010
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl132,465,108 - 32,485,568 (+)Ensembl
RefSeq Acc Id: NM_001145720   ⟹   NP_001139192
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38132,465,072 - 32,496,686 (+)NCBI
GRCh37132,930,658 - 32,953,460 (+)RGD
Celera131,198,480 - 31,221,280 (+)RGD
HuRef131,046,019 - 31,068,729 (+)ENTREZGENE
CHM1_1133,046,109 - 33,068,992 (+)NCBI
T2T-CHM13v2.0132,322,988 - 32,354,613 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001139192 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein CAH10660 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000476499
  ENSP00000476499.1
GenBank Protein Q8NAP8 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001139192   ⟸   NM_001145720
- UniProtKB: Q5VXR5 (UniProtKB/Swiss-Prot),   Q15DG5 (UniProtKB/Swiss-Prot),   Q69YT7 (UniProtKB/Swiss-Prot),   Q8NAP8 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000476499   ⟸   ENST00000609129
Ensembl Acc Id: ENSP00000601009   ⟸   ENST00000930950
Ensembl Acc Id: ENSP00000601008   ⟸   ENST00000930949
Ensembl Acc Id: ENSP00000601010   ⟸   ENST00000930951
Protein Domains
BTB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8NAP8-F1-model_v2 AlphaFold Q8NAP8 1-495 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:37057 AgrOrtholog
COSMIC ZBTB8B COSMIC
Ensembl Genes ENSG00000273274 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000609129 ENTREZGENE
  ENST00000609129.2 UniProtKB/Swiss-Prot
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot
  Potassium Channel Kv1.1, Chain A UniProtKB/Swiss-Prot
GTEx ENSG00000273274 GTEx
HGNC ID HGNC:37057 ENTREZGENE
Human Proteome Map ZBTB8B Human Proteome Map
InterPro BTB/POZ_dom UniProtKB/Swiss-Prot
  SKP1/BTB/POZ_sf UniProtKB/Swiss-Prot
  Znf_C2H2_sf UniProtKB/Swiss-Prot
  Znf_C2H2_type UniProtKB/Swiss-Prot
  ZnFinger_BTB_dom_contain UniProtKB/Swiss-Prot
KEGG Report hsa:728116 UniProtKB/Swiss-Prot
NCBI Gene 728116 ENTREZGENE
PANTHER AGAP004733-PA UniProtKB/Swiss-Prot
  ZGC:110075 PROTEIN UniProtKB/Swiss-Prot
Pfam BTB UniProtKB/Swiss-Prot
  zf-H2C2_2 UniProtKB/Swiss-Prot
PharmGKB PA164727642 PharmGKB
PROSITE BTB UniProtKB/Swiss-Prot
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot
SMART BTB UniProtKB/Swiss-Prot
  ZnF_C2H2 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF54695 UniProtKB/Swiss-Prot
  SSF57667 UniProtKB/Swiss-Prot
UniProt Q15DG5 ENTREZGENE
  Q5VXR5 ENTREZGENE
  Q69YT7 ENTREZGENE
  Q8NAP8 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary Q15DG5 UniProtKB/Swiss-Prot
  Q5VXR5 UniProtKB/Swiss-Prot
  Q69YT7 UniProtKB/Swiss-Prot