Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23619
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger imprinted 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZIM2
Synonyms (NCBI Gene) Gene synonyms aliases
ZNF656
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.43
Summary Summary of gene provided in NCBI Entrez Gene.
In human, ZIM2 and PEG3 (GeneID:5178) are two distinct genes that share a set of 5` exons and have a common promoter, and both genes are paternally expressed. Alternative splicing events connect the shared exons either with the remaining 4 exons unique to
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1513615 hsa-miR-409-3p CLIP-seq
MIRT1513616 hsa-miR-4266 CLIP-seq
MIRT1513617 hsa-miR-4695-5p CLIP-seq
MIRT1513618 hsa-miR-4779 CLIP-seq
MIRT1513619 hsa-miR-4786-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0003700 Function DNA-binding transcription factor activity NAS 34673265
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IEA
GO:0006355 Process Regulation of DNA-templated transcription IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q9NZV7
Protein name Zinc finger imprinted 2 (Zinc finger protein 656)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 175 216 KRAB box Family
PF13894 zf-C2H2_4 328 351 Domain
PF00096 zf-C2H2 466 488 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 494 516 Zinc finger, C2H2 type Domain
Tissue specificity TISSUE SPECIFICITY: Highest levels of expression in adult testis; modest levels in fetal kidney and brain.
Sequence
MYQPEDDNNSDVTSDDDMTRNRRESSPPHSVHSFSGDRDWDRRGRSRDMEPRDRWSHTRN
PRSRMPPRDLSLPVVAKTSFEMDREDDRDSRAYESRSQDAESYQNVVDLAEDRKPHNTIQ
DNMENYRKLLSLGFLAQDSVPAEKRNTEMLDNLPSAGSQFPDFKHLGTFLVFEELVTFED
VLVDFSPEELSSLSAAQRNLYREVMLENYRNLVSLG
HQFSKPDIISRLEEEESYAMETDS
RHTVICQGESHDDPLEPHQGNQEKLLTPITMNDPKTLTPERSYGSDEFERSSNLSKQSKD
PLGKDPQEGTAPGICTSPQSASQENKHNRCEFCKRTFSTQVALRRHERIHTGKKPYECKQ
CAEAFYLMPHLNRHQKTHSGRKTSGCNEGRKPSVQCANLCERVRIHSQEDYFECFQCGKA
FLQNVHLLQHLKAHEAARVLPPGLSHSKTYLIRYQRKHDYVGERACQCCDCGRVFSRNSY
LIQHYRTH
TQERPYQCQLCGKCFGRPSYLTQHYQLHSQEKTVECDHC
Sequence length 527
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Prostate cancer Prostate cancer N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Uterine Diseases Associate 36552753