Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
58495
Gene name Gene Name - the full gene name approved by the HGNC.
Ovo like zinc finger 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
OVOL2
Synonyms (NCBI Gene) Gene synonyms aliases
CHED, CHED1, CHED2, EUROIMAGE566589, PPCD1, ZNF339
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20p11.23
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intr
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs869320627 ->GGTTCCGGCGGCCGGGGCTGCC Pathogenic Intron variant, upstream transcript variant, genic upstream transcript variant
rs869320628 A>G Pathogenic Intron variant, upstream transcript variant, genic upstream transcript variant
rs869320629 A>G Pathogenic Intron variant, upstream transcript variant, genic upstream transcript variant
rs869320630 A>C Pathogenic Intron variant, 5 prime UTR variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1208409 hsa-miR-1197 CLIP-seq
MIRT1208410 hsa-miR-1237 CLIP-seq
MIRT1208411 hsa-miR-1248 CLIP-seq
MIRT1208412 hsa-miR-1275 CLIP-seq
MIRT1208413 hsa-miR-188-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0000976 Function Transcription cis-regulatory region binding IDA 19700410
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0001227 Function DNA-binding transcription repressor activity, RNA polymerase II-specific IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616441 15804 ENSG00000125850
Protein
UniProt ID Q9BRP0
Protein name Transcription factor Ovo-like 2 (hOvo2) (Zinc finger protein 339)
Protein function Zinc-finger transcription repressor factor (PubMed:19700410). Plays a critical role in maintaining the identity of epithelial lineages by suppressing epithelial-to mesenchymal transition (EMT) mainly through the repression of ZEB1, an EMT induce
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13894 zf-C2H2_4 147 170 Domain
PF00096 zf-C2H2 175 198 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 214 237 Zinc finger, C2H2 type Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in testis, ovary, heart and skeletal muscle (PubMed:12213202). Expressed in the cornea, but absent from the corneal endothelium (PubMed:26749309). {ECO:0000269|PubMed:12213202, ECO:0000269|PubMed:26749309}.
Sequence
MPKVFLVKRRSLGVSVRSWDELPDEKRADTYIPVGLGRLLHDPPEDCRSDGGSSSGSGSS
SAGEPGGAESSSSPHAPESETPEPGDAEGPDGHLATKQRPVARSKIKFTTGTCSDSVVHS
CDLCGKGFRLQRMLNRHLKCHNQVKRHLCTFCGKGFNDTFDLKRHVRTHTGIRPYKCNVC
NKAFTQRCSLESHLKKIH
GVQQQYAYKQRRDKLYVCEDCGYTGPTQEDLYLHVNSAHPGS
SFLKKTSKKLAALLQGKLTSAHQENTSLSEEEERK
Sequence length 275
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Polymorphous corneal dystrophy Posterior polymorphous corneal dystrophy 1 rs869320627, rs869320628, rs869320629, rs869320630 N/A
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
Congenital Hereditary Endothelial Dystrophy congenital hereditary endothelial dystrophy type I N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alopecia Associate 26873447
Bowen's Disease Stimulate 28339425
Breast Neoplasms Associate 38066300
Carcinogenesis Associate 37138231
Carcinoma Ovarian Epithelial Associate 36149163
Carcinoma Squamous Cell Associate 28339425
Corneal Dystrophy Posterior Polymorphous 1 Associate 19574904, 26749309, 27355326, 28046031, 28654985, 29499165
Corneal endothelial dystrophy type 2 Associate 26749309, 40225920
Hair Diseases Associate 26873447
Nasopharyngeal Carcinoma Associate 29721073