Gene Gene information from NCBI Gene database.
Entrez ID 7709
Gene name Zinc finger and BTB domain containing 17
Gene symbol ZBTB17
Synonyms (NCBI Gene)
MIZ-1ZNF151ZNF60pHZ-67
Chromosome 1
Chromosome location 1p36.13
Summary This gene encodes a zinc finger protein involved in the regulation of c-myc. The symbol MIZ1 has also been associated with PIAS2 which is a different gene located on chromosome 18. [provided by RefSeq, Jul 2008]
miRNA miRNA information provided by mirtarbase database.
2
miRTarBase ID miRNA Experiments Reference
MIRT439262 hsa-miR-544a HITS-CLIP 24374217
MIRT439262 hsa-miR-544a HITS-CLIP 24374217
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IBA
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IMP 9312026
GO:0001046 Function Core promoter sequence-specific DNA binding IDA 19160485
GO:0001223 Function Transcription coactivator binding IPI 19160485
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604084 12936 ENSG00000116809
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q13105
Protein name Zinc finger and BTB domain-containing protein 17 (Myc-interacting zinc finger protein 1) (Miz-1) (Zinc finger protein 151) (Zinc finger protein 60)
Protein function Transcription factor that can function as an activator or repressor depending on its binding partners, and by targeting negative regulators of cell cycle progression. Plays a critical role in early lymphocyte development, where it is essential t
PDB 2LVR , 2LVT , 2LVU , 2M0D , 2M0E , 2M0F , 2N25 , 2N26 , 2Q81 , 3M52 , 4U2M , 4U2N , 5ION , 7AZW , 7AZX , 7MC1 , 7MC2 , 7MC3 , 7T58
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00651 BTB 14 113 BTB/POZ domain Domain
PF00096 zf-C2H2 306 328 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 390 412 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 418 440 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 446 468 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 474 496 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 530 552 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 558 580 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 586 608 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 614 637 Zinc finger, C2H2 type Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in germinal center B-cells. {ECO:0000269|PubMed:16142238}.
Sequence
MDFPQHSQHVLEQLNQQRQLGLLCDCTFVVDGVHFKAHKAVLAACSEYFKMLFVDQKDVV
HLDISNAAGLGQVLEFMYTAKLSLSPENVDDVLAVATFLQMQDIITACHALKS
LAEPATS
PGGNAEALATEGGDKRAKEEKVATSTLSRLEQAGRSTPIGPSRDLKEERGGQAQSAASGA
EQTEKADAPREPPPVELKPDPTSGMAAAEAEAALSESSEQEMEVEPARKGEEEQKEQEEQ
EEEGAGPAEVKEEGSQLENGEAPEENENEESAGTDSGQELGSEARGLRSGTYGDRTESKA
YGSVIHKCEDCGKEFTHTGNFKRHIRIHTGEKPFSCRECSKAFSDPAACKAHEKTHSPLK
PYGCEECGKSYRLISLLNLHKKRHSGEARYRCEDCGKLFTTSGNLKRHQLVHSGEKPYQC
DYCGRSFSDPTSKMRHLETH
DTDKEHKCPHCDKKFNQVGNLKAHLKIHIADGPLKCRECG
KQFTTSGNLKRHLRIH
SGEKPYVCIHCQRQFADPGALQRHVRIHTGEKPCQCVMCGKAFT
QASSLIAHVRQH
TGEKPYVCERCGKRFVQSSQLANHIRHHDNIRPHKCSVCSKAFVNVGD
LSKHIIIH
TGEKPYLCDKCGRGFNRVDNLRSHVKTVHQGKAGIKILEPEEGSEVSVVTVD
DMVTLATEALAATAVTQLTVVPVGAAVTADETEVLKAEISKAVKQVQEEDPNTHILYACD
SCGDKFLDANSLAQHVRIHTAQALVMFQTDADFYQQYGPGGTWPAGQVLQAGELVFRPRD
GAEGQPALAETSPTAPECPPPAE
Sequence length 803
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Cell cycle
Pathways in cancer
Transcriptional misregulation in cancer
Small cell lung cancer
  XBP1(S) activates chaperone genes
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
16
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs12134932 RCV005919936
Cholangiocarcinoma Benign rs12134932 RCV005919942
Malignant lymphoma, large B-cell, diffuse Benign rs12134932 RCV005919939
Nonpapillary renal cell carcinoma Benign rs12134932 RCV005919937
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Cardiomyopathy Dilated Associate 21459883, 23570452, 28296976
Colonic Neoplasms Associate 37370088
familial dilated cardiomyopathy Associate 21459883
Oligodendroglioma Associate 29890994
Stomach Neoplasms Associate 31151932