Gene Gene information from NCBI Gene database.
Entrez ID 23144
Gene name Zinc finger CCCH-type containing 3
Gene symbol ZC3H3
Synonyms (NCBI Gene)
SMICLZC3HDC3
Chromosome 8
Chromosome location 8q24.3
miRNA miRNA information provided by mirtarbase database.
68
miRTarBase ID miRNA Experiments Reference
MIRT040908 hsa-miR-18a-3p CLASH 23622248
MIRT039752 hsa-miR-615-3p CLASH 23622248
MIRT1505864 hsa-miR-1238 CLIP-seq
MIRT1505865 hsa-miR-125a-3p CLIP-seq
MIRT1505866 hsa-miR-1908 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IDA 16115198, 19364924
GO:0005634 Component Nucleus IEA
GO:0005847 Component MRNA cleavage and polyadenylation specificity factor complex IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618640 28972 ENSG00000014164
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IXZ2
Protein name Zinc finger CCCH domain-containing protein 3 (Smad-interacting CPSF-like factor)
Protein function Required for the export of polyadenylated mRNAs from the nucleus (PubMed:19364924). Enhances ACVR1B-induced SMAD-dependent transcription. Binds to single-stranded DNA but not to double-stranded DNA in vitro. Involved in RNA cleavage (By similari
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00642 zf-CCCH 668 694 Zinc finger C-x8-C-x5-C-x3-H type (and similar) Family
PF00642 zf-CCCH 773 798 Zinc finger C-x8-C-x5-C-x3-H type (and similar) Family
Sequence
MEEKEILRRQIRLLQGLIDDYKTLHGNAPAPGTPAASGWQPPTYHSGRAFSARYPRPSRR
GYSSHHGPSWRKKYSLVNRPPGPSDPPADHAVRPLHGARGGQPPVPQQHVLERQVQLSQG
QNVVIKVKPPSKSGSASASGAQRGSLEEFEETPWSDQRPREGEGEPPRGQLQPSRPTRAR
GTCSVEDPLLVCQKEPGKPRMVKSVGSVGDSPREPRRTVSESVIAVKASFPSSALPPRTG
VALGRKLGSHSVASCAPQLLGDRRVDAGHTDQPVPSGSVGGPARPASGPRQAREASLVVT
CRTNKFRKNNYKWVAASSKSPRVARRALSPRVAAENVCKASAGMANKVEKPQLIADPEPK
PRKPATSSKPGSAPSKYKWKASSPSASSSSSFRWQSEASSKDHASQLSPVLSRSPSGDRP
AVGHSGLKPLSGETPLSAYKVKSRTKIIRRRSSTSLPGDKKSGTSPAATAKSHLSLRRRQ
ALRGKSSPVLKKTPNKGLVQVTTHRLCRLPPSRAHLPTKEASSLHAVRTAPTSKVIKTRY
RIVKKTPASPLSAPPFPLSLPSWRARRLSLSRSLVLNRLRPVASGGGKAQPGSPWWRSKG
YRCIGGVLYKVSANKLSKTSGQPSDAGSRPLLRTGRLDPAGSCSRSLASRAVQRSLAIIR
QARQRREKRKEYCMYYNRFGRCNRGERCPYIHDPEKVAVCTRFVRGTCKKTDGTCPFSHH
VSKEKMPVCSYFLKGICSNSNCPYSHVYVSRKAEVCSDFLKGYCPLGAKCKKKHTLLCPD
FARRGACPRGAQCQLLHR
TQKRHSRRAATSPAPGPSDATARSRVSASHGPRKPSASQRPT
RQTPSSAALTAAAVAAPPHCPGGSASPSSSKASSSSSSSSSPPASLDHEAPSLQEAALAA
ACSNRLCKLPSFISLQSSPSPGAQPRVRAPRAPLTKDSGKPLHIKPRL
Sequence length 948
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
5
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Colon adenocarcinoma Uncertain significance rs373613798 RCV005931226
Decreased total lymphocyte count Likely benign rs149025999, rs145312531 RCV002227878
RCV002227879
Decreased total neutrophil count Likely benign rs149025999, rs145312531 RCV002227878
RCV002227879
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adrenocortical Carcinoma Associate 33725886
Carcinoma Hepatocellular Associate 33059309
Carcinoma Hepatocellular Stimulate 38302914
Fibrosis Associate 38302914
Precancerous Conditions Associate 36471401
Retinal Vein Occlusion Associate 33059309