Gene Gene information from NCBI Gene database.
Entrez ID 9923
Gene name Zinc finger and BTB domain containing 40
Gene symbol ZBTB40
Synonyms (NCBI Gene)
ZNF923
Chromosome 1
Chromosome location 1p36.12
miRNA miRNA information provided by mirtarbase database.
1002
miRTarBase ID miRNA Experiments Reference
MIRT036494 hsa-miR-1226-3p CLASH 23622248
MIRT651362 hsa-miR-6887-3p HITS-CLIP 23824327
MIRT651361 hsa-miR-6795-3p HITS-CLIP 23824327
MIRT651360 hsa-miR-6734-3p HITS-CLIP 23824327
MIRT651359 hsa-miR-4297 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 28169274
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IDA 15302935
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612106 29045 ENSG00000184677
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NUA8
Protein name Zinc finger and BTB domain-containing protein 40
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00651 BTB 14 116 BTB/POZ domain Domain
PF00096 zf-C2H2 836 858 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 893 915 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 921 944 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 978 1000 Zinc finger, C2H2 type Domain
PF12874 zf-met 1135 1157 Domain
Sequence
MELPNYSRQLLQQLYTLCKEQQFCDCTISIGTIYFRAHKLVLAAASLLFKTLLDNTDTIS
IDASVVSPEEFALLLEMMYTGKLPVGKHNFSKIISLADSLQMFDVAVSCKNLLTSL
VNCS
VQGQVVRDVSAPSSETFRKEPEKPQVEILSSEGAGEPHSSPELAATPGGPVKAETEEAAH
SVSQEMSVNSPTAQESQRNAETPAETPTTAEACSPSPAVQTFSEAKKTSTEPGCERKHYQ
LNFLLENEGVFSDALMVTQDVLKKLEMCSEIKGPQKEMIVKCFEGEGGHSAFQRILGKVR
EESLDVQTVVSLLRLYQYSNPAVKTALLDRKPEDVDTVQPKGSTEEGKTLSVLLLEHKED
LIQCVTQLRPIMESLETAKEEFLTGTEKRVILNCCEGRTPKETIENLLHRMTEEKTLTAE
GLVKLLQAVKTTFPNLGLLLEKLQKSATLPSTTVQPSPDDYGTELLRRYHENLSEIFTDN
QILLKMISHMTSLAPGEREVMEKLVKRDSGSGGFNSLISAVLEKQTLSATAIWQLLLVVQ
ETKTCPLDLLMEEIRREPGADAFFRAVTTPEHATLETILRHNQLILEAIQQKIEYKLFTS
EEEHLAETVKEILSIPSETASPEASLRAVLSRAMEKSVPAIEICHLLCSVHKSFPGLQPV
MQELAYIGVLTKEDGEKETWKVSNKFHLEANNKEDEKAAKEDSQPGEQNDQGETGSLPGQ
QEKEASASPDPAKKSFICKACDKSFHFYCRLKVHMKRCRVAKSKQVQCKECSETKDSKKE
LDKHQLEAHGAGGEPDAPKKKKKRLPVTCDLCGREFAHASGMQYHKLTEHFDEKPFSCEE
CGAKFAANSTLKNHLRLH
TGDRPFMCKHCLMTFTQASALAYHTKKKHSEGKMYACQYCDA
VFAQSIELSRHVRTH
TGDKPYVCRDCGKGFRQANGLSIHLHTFHNIEDPYDCKKCRMSFP
TLQDHRKHIHEVHSKEYHPCPTCGKIFSAPSMLERHVVTHVGGKPFSCGICNKAYQQLSG
LWYHNRTHHPDVFAAQNHRSSKFSSLQCSSCDKTFPNTIEHKKHIKAEHADMKFHECDQC
KELFPTPALLQVHVKCQHSGSQPFRCLYCAATFRFPGALQHHVTTEHFKQSETTFPCELC
GELFTSQAQLDSHLESE
HPKVMSTETQAAASQMAQVIQTPEPVAPTEQVITLEETQLAGS
QVFVTLPDSQASQASSELVAVTVEDLLDGTVTLICGEAK
Sequence length 1239
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
11
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Likely benign rs374282664 RCV005935594
Clear cell carcinoma of kidney Uncertain significance rs551375407 RCV005931010
ZBTB40-related disorder Likely benign; Benign rs577900930, rs371758282, rs374357053, rs142695294, rs182939277, rs34216459, rs374282664, rs881646, rs36115661 RCV003981769
RCV003967323
RCV003909800
RCV003941956
RCV003959665
RCV003936916
RCV003981803
RCV003982207
RCV003972856
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Inflammatory Bowel Diseases Associate 36155972, 36680554
Osteoporosis Associate 22824048, 30013441
Pediatric Obesity Associate 35546387